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Stoichiometry and Redox Reactions

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Stoichiometry and Redox Reactions

EXERCISE 1 JEE MAIN/BOARDS


MOLE CONCEPT are in accordance with the law of conservation
Q.1 Express the following in S.I. units: of mass.
(i) 125 pounds, the average weight of an Q.11 A chloride of phosphate contains 22.57%
P. Phosphine contains 8.82% hydrogen and
Indian boy (1 b = 545 g)
hydrogen chloride gas contain 97.26% chlorine.
(ii) 14 b/m2 (atmospheric pressure)
Show that the data illustrate law of reciprocal
(iii) 5'8", the average height of ramp models.
proportions.
P
Q.2 The isotropic distribution of potassium is (22.57) (91.38)

39 41 41
93.2% K and 6.8% K . How many K atoms
are there in 2g-atoms?
(77.43) (8.82)
Q.3 How many oxygen atoms are present in Cl
(97.26)
H
(2.77)
6.025 g of Barium phosphate (at. mass of
Ba=137.5, P= 31, O = 16 amu) Q.12 1.375 g of cupric oxide was reduced by
heating in a current of hydrogen and the mass
Q.4 The vapour density of a mixture containing of copper that remained was 1.098 g. In
NO2 and N2O4 is 3.83 at 27ºC. another experiment, 1.179 g of copper was
Calculate the moles of NO2 in 100 g mixture. dissolved in the nitric acid and the resulting
copper nitrate converted into cupric oxide by
Q.5 Assume that the nucleus of the F atom is a ignition. The mass of cupric oxide formed was
3
sphere of radius 5  10 cm. Calculate the 1.476 g. Show that these results illustrate the
density of matter in F nucleus. (At. mass F= 19) law of constant composition.

Q.6 20.0 mL of Dil. HNO3 is neutralised Q.13 1.020 g of metallic oxide contains 0.540 g
completely with 25 mL of 0.08 M NaOH. What of the metal. Calculate the equivalent mass of
is molarity of HNO3 ? the metal and hence its atomic mass with the
help of Dulong and Petit's law. Taking the
Q.7 Gastric juice containing 3.0 g of HCl per symbol for the metal as M, find the molecular
litre. If a person produces about 2.5 litres of formula of the oxide. The specific heat of the
gastric juice a per day, how many antacid metal is 0.216 cal deg–1 g–1.
tablets each containing 400 mg of Al(OH)3 are
Q.14 Potassium per magnate is a dark green
needed to neutralise all the HCl produced in crystalline substance whose composition is
one day. 39.7% K, 29.9% Mn and rest O. Find the
Q.8 10 mL of HCl solution produced 0.1435 g empirical formula?
of AgCl when treated with excess of Silver Q.15 Calculate the molarity of pure water at
nitrate solution. What is the Molarity of acid 4ºC.
solution [at. mass Ag = 100].
Q.16 (a) What is the mass in grams of one
Q.9 A certain compound containing only molecule of caffeine (C8H20N4O2 ) ?
carbon and oxygen. Analysis show it has 36%
(b) Determine the total number of electrons in
carbon and 64% oxygen. If its molecular mass
0.142 g Cl2 .
is 400 then what is the molecular formula of the
compound. Q.17 Calculate the molarity of distilled water if
Q.10 0.44 g of a hydro carbon an complete its density is 103 kg / m3 .
combustion which oxygen gave 1.8 g water and
0.88 g carbon dixoide. Show that these results Q.18 A plant virus if found to consist of uniform
cylindrical particles of 150 Å in diameter and

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Stoichiometry and Redox Reactions

5000 Å long. The specific volume of virus is 0.75 Q.26 Equal masses of zinc (at. mass 65) and
cm3/g. If the virus is considered to be a simple iodine (at. mass 127) were allowed to react till
particle, find the its molecular weight. completion of reaction to form ZnI2. Which
substance is left unreacted and to what fraction
Q.19 Calculate the mass of two litre sample of
of its original mass?
water containing 25% heavy water (D2O) in it
by volume. Density of H2 O is 1.0 gcm–3 whereas Q.27 Two gram each of P4 and O2 are allowed
that of D2 O is 1.06 gmc–3. to react till none of the reactant is left. If the
products are P4 O6 and P4O10 .Calculate the
Q.20 2.5 moles of sulphuryl chloride were mass of each of the product.
dissolved in water to produce sulphuric acid
and hydrochloric acid. How many moles of KOH Q.28 A piece of aluminium weighing 2.7 g was
will be required to completely neutralise the heated with 100 mL of H2SO4 (25% by mass, d
solution? = 1.18 g cm–3). After complete dissolution of
metal, the solution is diluted by adding water
Q.21 100 g of a sample of common salt
to 500 ml. What is the molarity of free H2SO4 in
containing contamination of NH4Cl and MgCl2
resulting solution?
to the extent of 2% each by mass is dissolved in
water. How much volume of 5% by mass of Q.29 Chemical reaction between ferrous
AgNO3 solution (d = 1.04 g cm–3) is required to oxalate and KMnO4 has been given in the form
precipitate all chloride ions? of three partial equations. Write the complete
balanced equation and thus find out the
Q.22 A mixture of formic acid and oxalic acid is
volume of 0.5 M KMnO4 required to
heated with concentrated H2SO4 . The gases
completely react with 1.5 mol of FeC2O4 .
produced are collected and on treatment with
KOH solution, the volume of the gases KMnO4  H2SO4 
decreased by 1.6th. Calculate the molar ratio of K 2SO4  MnSO4  H2O  (O)
the two acids in the original mixture.
FeC 2O 4  H 2SO 4  FeSO4  H 2C2O4
Q.23 The mean molecular mass of a mixture of
methane (CH4 ) and ethene (C 2H4 ) in the FeSI4  H 2C 2O 4  H2SO 4  O 
molar ratio of x: y is found to be 20. What will Fe 2 (SO4 )3  CO2  H2
be the mean molecular mass if the molar ratio
of the gases is reversed?

Q.24 1 g sample of KClO3 was heated under


such conditions that a part of it decomposes a
2KClO3  2KCl  3O2 while the remaining
part decomposes as
4KClO3  3KClO4  KCl.
If net oxygen obtained is 146.8 ml at STP.
Calculate the mass of KClO4 in the residue.

Q.25 A mixture of FeO and Fe3O4 was heated


in air to constant mass and it was found to gain
5% in its mass. Find the composition of the
initial mixture.

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Stoichiometry and Redox Reactions

REDOX REACTIONS (b) Cu2  I  Cu  I2


Q.1 Indicate the oxidation number of (c) CuO  NH3  Cu  N2  H2O
underlined in each case: 2 3
(d) H2SO3  Cr2O7 H2SO4  Cr  H2O
(a) (N2H5 ) 2 SO4 (b) Mg3 N2
(Acid medium)
(c) [Co(NH3 )5 Cl]Cl2 (d) K 2 FeO4 2
(e) Cr2O7

 C2H4O  H  C 2H4O2  Cr 3
(e) Ba(H2 PO2 ) 2 (f) H2 SO4 (Acid medium)
(g) CS2 (h) S 2 (f)
(i) Na 2 S4O6 (j) S2Cl6 SbCl3  KIO3  HCl  SbCl3  ICl  H2O  KCl
(k) RNO2 (l) Pb 3 O4
2 (Acid medium)
(m) S2 O 8 (n) C6H12O6
(o) Mg2 P 2O7 (p) KClO3 Q.5 Define disproportionation? Give one
example.
Q.2 Write complete balanced equation for the
Q.6 Define difference between ion electron
following in acidic medium by ion-electron
method and oxidation method?
method:
  
(a) Br  BrO3  H  Br2  H2O Q.7 What is the most essential conditions that
must be satisfied in a redox reaction?
(b) H2S  Cr3 O72  H  Cr2O3  S8  H2O
(c) Q.8 Does the oxidation number of an element
in any molecule or any poly atomic ion
Au  NO3  
 Cl  H  AuCl4  NO3  H2O
represents the actual charge on it?
  2
(d) Cu 2O  H  NO3  Cu  NO  H2O
2 1 Q.9 What is redox couple?
(e) MnO4  MnO4  MnO2
2  2 Q.10 Calculate the standard e.m.f. of the cells
(f) Cu  SO2  Cu  SO4
formed by different combinations of the
 
(g) Cl2  I2 IO3  Cl following half cells.
(h) Zn(g) / Zn2(aq)
Fe(CN)64  MnO4 Fe 3  CO2  NO3  Mn 2 Cu(s) / Cu2(aq)
2 2 3
(i) Cu3P  Cr2O7  Cu  H3PO4  Cr Ni(s) / Ni2(aq)
Q.3 Write complete balanced equation for the Ag(s) / Ag2(aq)
following in basic medium by ion-electron
method: Q.11 Balance the following equations in acidic
(a)
2 
Cu  I  Cu  I2  medium by both oxidation number & ion
 electron methods & identify the oxidants & the
(b) Fe 3 O4  MnO4 Fe 2O3  MnO2 reductants.
(c) (a)
C2H5 OH  MnO4  C2H3 O  MnO2 (s)  H2O MnO4 (aq)  C2H2O4(aq) Mn(aq)
2
 CO2(g)  H2O( l )
 2 
(d) CrI3  H2O2  OH  CrO4  IO4  H2O (b) H2S(aq)  Cl2(g) S(s)  Cl(aq)
(e) KOH  K 4Fe(CN)6  Ce(NO3 ) 4 
Q.12 Balance the following equations in basic
Fe(OH)3  Ce(OH)3  K 2CO3  KNO3  H2O medium by both oxidation number & ion
electron methods. Identify the reductants & the
Q.4 Balance the following equations by
oxidants.
oxidation method:  
 (a) P(s)  OH(aq) PH1(s)  H2PO2(aq)
(a) I  H2O2 H2O  I2 (Acid medium)

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Stoichiometry and Redox Reactions


(b) N2H4(g)  ClO3(aq) NO(g)  Cl(aq)
Q.13 Define oxidation & reduction in term of
oxidation number.

Q.14 Discuss the following redox reactions?


(i) Combination reactions
(ii) Decomposition reactions
(iii) Displacement reactions
(iv) Disproportionation reaction

Q.15 What is an electrochemical series? How


can this be used to explain the oxidising &
reducing abilities of element?

Q.16 What is the difference between valence &


oxidation HO.

Q.17 H2S act only as a reductant as well as


oxidant explain?

Q.18 What are half reactions? Explain with


examples?

Q.19 Draw a labelled diagram for the daniel


cell. Discuss its working?

Q.20 Explain the term:


(i) Oxidation
(ii) Reduction
(iii) Oxidizing agent
(iv) Reducing agent

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Stoichiometry and Redox Reactions

EXERCISE 2 JEE MAIN

MOLE CONCEPT N2 and 2 volume of H2 at STP. The hydride of


Q.1 If 'x' gms of an element A reacts with 16 nitrogen is
gms of oxygen then the equivalent weight of (A) NH3 (B) N2H6 (C) NH2 (D) N2H4
element A is
x x Q.8 5 volumes of a hydrocarbon on complete
(A) (B) (C) x (D) 2x consumed 10 volumes of oxygen giving 5
4 2 volumes of CO2 at STP. The hydrocarbon is
Q.2The mass of CO containing the same (A) C2H6 (B) C2H4 (C) CH4 (D) C2H4
amount of oxygen as in 88 gms of CO2 is
(A) 56 gms (B) 28 gms (C) 112 gms(D) 14 gms Q.9 The percentage by mole of NO2 in a
mixture of NO2 (g) and NO(g) having average
Q.3 When 8 gms of oxygen reacts with
magnesium then the amount of MgO formed is molecular mass 34 is
(A) 18 gm (B) 20 gm (C) 24 gm (D) 32 gm (A) 25% (B) 20% (C) 40% (D) 75%

Q.4 One gram of the silver salt of an organic Q.10 The minimum mass of mixture of A2 and
dibasic acid yields, on strong heating 0.5934 g B4 required to produce at least 1 kg of each
of silver. If the weight percentage of carbon in product is
it 8 times the weight percentage of hydrogen (Given At. mass of 'A' = 10; At. mass of 'B' =
and one half the weight percentage of oxygen, 120) 5A 2  2B4  2AB2  4A 2B
determine the molecular formula of the acid.
(A) 2120 gm (B) 1060 gm
[Atomic weight of Ag = 108]
(C) 560 gm (D) 1660 gm
(A) C4H6 O4 (B) C4H6 O6
(C) C2H6O2 (D) C5H10O5 Q.11 74 gm of a sample on complete
combustion given 132 gm CO2 and 54 gm of
Q.5 Mass of sucrose C12H22O11 produced by H2 O . The molecular formula of the compound
mixing 84 gm of carbon, 12 gm of hydrogen may be
and 56 lit. O2 at 1 atm & 273 K according to (A) C5H12 (B) C4H10 O
given reaction, is (C) C3H6 O2 (D) C3H7 O2
C(s)  H2 (g)  O2 (g)  C12H22O11(s)
(A) 138.5 (B) 155.5 Q.12 The volume of oxygen used when x gms
(C) 172.5 (D) 199.5 of Zn is converted to ZnO is
x2 x
Q.6 40 gm of carbonate of an alkali metal or (A)  5.6 litres (B)  5.6 litres
65 65
alkaline earth metal containing some inert 4x
impurities was made to react with excess HCl (C)  5.6 litres (D) None of these
solution. The liberated CO2 occupied 12.315 lit. 65
at 1 atm & 300 K. The correct option is Q.13 A sample of clay was partially dried and
(A) Mass of impurity is 1 gm and metal is Be then contained 50% silica and 7% water. The
(B) Mass of impurity is 3 gm and metal is Li original clay contained 12% water. The silica is
(C) Mass of impurity is 5 gm and metal is Be original sample is
(D) Mass of impurity is 2 gm and metal is Mg (A) 51.69 (B) 47.31
(C) 63.31 (D) None of these
Q.7 An hydride of nitrogen decomposes to
give nitrogen and hydrogen. It was formed that Q.14 The mass of CO2 produced from 620
one volume of the hydride gave one volume of mixture of C2H4O2 & O2 , prepared produce

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Stoichiometry and Redox Reactions

maximum energy is (Combustion reaction is Q.22 The molarity of a solution of conc. HCl
exothermic) containing 36.5% by weight of HCl would be
(A) 413.33 gm (B) 593.04 gm (A) 16.75 (B) 17.75 (C) 15.75 (D) 14.75
(C) 440 gm (D) 320 gm
Q.23 0.35 gms of a sample of Na 2CO3 .xH2O
Q.15 In the quantitative determination of were dissolved in water and the volume was
nitrogen, N2 gas liberated from 0.42 gm of a made to 50 ml of this solution required 9.9 ml
sample of organic compound was collected of N/10 HCl for complete neutralization.
over water. If the volume of N2 gas collected Calculate the value of x.
was 100/11 ml at total pressure 860 mm Hg at (A) 1 (B) 2
250 K, % by mass of nitrogen in the organic (C) 3 (D) None of these
compound is Q.24 1.2 gms of a sample of washing soda was
[Aq. tension at 250 K is 24 mm Hg and R = dissolved in water and volume was made upto
0.08 L atm mol–1 K–1] 250 cc. 25 cc of this solution when titrated
10 5 20 100 against N/10 HCl for required 17 ml. The
(A) % (B) % (C) % (D) %
3 3 3 3 percentage of carbonate is given sample is
(A) Approximately 70%
Q.16 300 mlof 0.1 M HCl and 200 ml of 0.3 M
(B) Approximately 66%
H2SO4 are mixed. The normality of the (C) Approximately 76%
resulting mixture is (D) None of these
(A) 0.4 N (B) 0.1 N (C) 0.3 N (D) 0.2 N
Q.25 The number of carbon atoms present in a
Q.17 The volume of water which should be signature, if a signature written by carbon
added to 300 ml of 0.5 M NaOH solution so as pencil weights 1.2 × 10–3 g is
to get a solution of 0.2 M is
(A) 12.40  10 20 (B) 6.02 1019
(A) 550 ml (B) 350 ml (C) 750 ml (D) 450 ml
(C) 3.01 10 (D) 6.02  10
19 20

Q.18 The mole fraction of a solution containing


3.0 gms of urea per 250 gms of water would be Q.26 The average atomic mass of a mixture
24
(A) 0.00357 (B) 0.99643 containing 79 mole % of Mg, is 24.31. % mole
(C) 0.00643 (D) None of these of
26
Mg is
Q.19 The mass of P4O10 produced if 440 gm of (A) 5 (B) 20 (C) 10 (D) 15
P4S3 is mixed with 384 gm of O2 is Q.27 25 cc of solution containing NaOH and
P4S3  O2 P4O10  SO2 Na 2CO3 when titrated against N/10 HCl. Using
(A) 568 gm (B) 426 gm (C) 284 gm (D) 396 gm phenolphthalein as indicator required 40 cc. of
HCl. The same volume of mixture when titrated
Q.20 Calculate percentage change in Mavg of against N/10 HCl using methyl orange required
the mixture, if PCl5 undergo 50% 45cc of this HCl. The amount of NaOH and
Na 2CO3 in one mixture is
decomposition.
(A) NaOH = 28 gm/L ; Na 2 CO3 = 10.6 gm/L
PCl5 PCl3  Cl2
(B) NaOH = 10.6 gm/L ; Na 2 CO3 = 28 gm/L
(A) 50% (B) 66.66% (C) 33.33% (D) Zero
(C) NaOH = 14 gm/L ; Na 2 CO3 = 5.3 gm/L
Q.21 The mass of Mg3N2 produced if 48 gm of
(D) None of these
Mg metal is reacted with 34 gm NH3 gas is
Q.28 0.5 gms of a mixture of K 2CO3 and
Mg  NH3 Mg3N2  H2
Li2CO3 requires 30 ml of 0.25 NHCl solution for
200 100 400 150
(A) (B) (C) (D) neutralization. The percentage composition of
3 3 3 3 mixture would be

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Stoichiometry and Redox Reactions

(A) K 2CO3 = 96%; Li2CO3 = 4% REDOX REACTION


(B) K 2 CO3 = 4%; Li2CO3 = 96%
(C) K 2 CO3 = 50%; Li2CO3 = 25% Q.1 The equivalent weight of FeSO4 when it is
(D) K 2 CO3 = 50%; Li2CO3 = 74% oxidised by acidified KMnO4 will be equal to
Q.29 How many ml of a 0.05 M KMnO4 solution M0FeSO 4
(A) M0 of FeSO4 (B)
are required to oxidise 2.0 g of FeSO 4 in a 2
dilute acid solution? M0FeSO 4
(C) 2M0 FeSO4 (D)
(A) 5.263 (B) 0.5263 4
(C) 52.63 (D) None of these
Q.2 The equivalent weight of K 2Cr2O7 when it
Assertion Reason: 3
is converted Cr will be equal to
(A) If both statement-I and statement-II are true
MK 2Cr2O7
and statement II is the correct explanation of (A) MK 2Cr2O7 (B)
Statement I, the mark (A). 3
(B) If both statement-I and statement-II are true MK 2Cr2O7 MK 2Cr2O7
and statement II is not the correct explanation (C) (D)
4 6
of Statement I, the mark (B).
(C) If statement-I is true but Statement-II is Q.3 The amount of H2S that can be oxidised
false, then mark (C). to sulfur on oxidation using 1.58 gm of KMnO4
(D) If both statement-I and statement-II are
as oxidising agent in acidic medium will be
false, then mark (D).
(A) 0.85 gms (B) 1.7 gms
Q.30 Statement-I: The percentage of nitrogen (C) 0.425 gms (D) None of these
in urea is 46%.
Q.4 The amount of nitric acid required to
Statement-II: Urea is ionic compound.
oxidise 127 gms of I2 to I2 O 5 will be ______.
Q.31 Statement-I: The oxidation state of central Assume that during the reaction HNO3 gets
sulfur of Na 2S2O3 is +6.
converted to NO2 .
Statement-II: Oxidation state of an element
(A) 12.7 (B) 3.15 (C) 315 (D) 31.5
should be determined form structure.
Q.5 10 ml of oxalic acid was completely
Q.32 Statement-I: Molarity of a solution and oxidised by 20 ml of 0.02 M KMnO4 . The
molality of a solution both change with density.
normality of oxalic acid solution is
Statement-II: Density of the solution changes
(A) 0.05 N (B) 0.1 N (C) 0.2 N (D) 0.025 N
when percentage by mass of solution changes.
Q.6 0.2 g of a sample of H2 O 2 required 10 ml
Q.33 Statement-1: 2A  3B C , 4/3 moles
of 'C' are always produced when 3 moles of 'A' of 1N KMnO4 in a titration in the presence of
and 4 moles of 'B' are added. H2SO4 . Purity of H2O2 is
Statement-2: 'B' is the liming reactant for the (A) 25% (B) 65%
given data. (C) 85% (D) None of these

Q.7 The number of moles of KMnO4 that will


be needed to react completely with one mole
of ferrous oxalate in acidic solution is
2 3 4
(A) (B) (C) (D) 1
5 5 5
Q.8 A metal oxide is reduced by heating it in a
stream of hydrogen. It is found that after

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Stoichiometry and Redox Reactions

complete reduction, 3.15 g of the oxide has (A) HClO (B) HClO2 (C) HClO3 (D) HClO4
yielded 1.05 g of the metal. We may deduce
that Q.18 If three electrons are lost by a metal iron
(A) the atomic weight of the metal is 8 M3 ,its final oxidation number would be
(B) the atomic weight of the metal is 4 (A) 0 (B) +2 (C) +5 (D) +6
(C) the equivalent weight of the metal is 4
(D) the equivalent weight of the metal is 8 Q.19 The oxidation number of Mn in MnO4 is
(A) +7 (B) –5 (C) –7 (D) +5
Q.9 Oxidation involves
(A) gain of electrons Q.20 The oxidation number of carbon in CHCl3
(B) loss of electrons
is
(C) increase in the valency of negative part
(A) +2 (B) +4 (C) +4 (D) –3
(D) decrease in the valency of positive part
2
Q.21 Pb loses two electrons in a reaction.
Q.10 The oxidation number of Cr in K 2Cr2O7
What will be the oxidation number of lead after
(A) +2 (B) –2 (C) +6 (D) –6 the reaction?
Q.11 When K 2Cr2O7 is converted into K 2Cr2O4 (A) +2 (B) 0 (C) +4 (D) –2
the change in oxidation number of Cr is Q.22 The oxidation number of carbon in
(A) 0 (B) 6 (C) 4 (D) 3 C12H 22O11 is
Q.12 White P reacts with caustic soda. The (A) 0 (B) –6 (C) +2 (D) +6
products are PH3 and NaH2PO2 . This reaction
Q.23 The oxidation state of sulphur in SO24 is
is an example of
(A) oxidation (B) reduction (A) +2 (B) +4 (C) +5 (D) +6
(C) oxidation and reduction(D) neutralization Q.24 If the following reaction 'X' is
Q.13 The oxidation number of carbon in CH2O MnO2  4H  X Mn2  H2O
   
is (A) 1 e (B) 2 e (C) 3 e (D) 4 e
(A) –2 (B) +2 (C) 0 (D) +4
Q.25 In the following reaction the value of 'x' is
Q.14 The oxidation number of C in CH4 , CH3 Cl, H2O  SO32  SO42  2H  x
CH2Cl2 , CHCl3 , and CCl4 are respectively    
(A) 4 e (B) 3 e (C) 2 e (D) 1 e
(A) 0,2, 2,4, 4 (B) 4, 2,0, 2, 4
(C) 2,4,0, 2, 4 (D) 4,2,0, 2, 4 Q.26 The oxidation state of sulphur is S 2 O72 is
(A) +6 (B) –6 (C) –2 (D) +2
Q.15 Which of the following reactions is not
redox type Q.27 The oxidation number and covalency of
(A) 2BaO  O2  2BaO2 sulphur in S 8 are respectively
(B) 4KClO3  2KClO4  KCl (A) 0 and 2 (B) 0 and 8
(C) 6 and 8 (D) 6 and 2
(C) BaO2  H2SO4  BaSO4  H2O2
Q.28 The oxidation state of nitrogen in N3H is
(D) SO2  2H2 S  2H2 O  3S
(A) 1/3 (B) +3 (C) –1 (D) –1/3
Q.16 In which of the following compounds iron
Q.29 The oxidation number of iron in potassium
has lowest oxidation state
ferricyanide is
(A) K 4Fe(CN)6 (B) K 2FeO4
(A) +1 (B) +2 (C) +3 (D) +4
(C) Fe 2O (D) Fe(CO)5
Q.30 Oxidation number of hydrogen in MH2 is
Q.17 Select the compound in which chlorine is (A) +1 (B) –1 (C) +2 (D) –2
assigned the oxidation number +5

1.8
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Stoichiometry and Redox Reactions

Q.31 The oxidation state of phosphorus varies


from
(A) –1 to +1 (B) –3 to +3
(C) –3 to +5 (D) –5 to +1

Q.32 Select the compound in which chlorine is


assigned the oxidation number +5
(A) HClO4 (B) HClO2 (C) HClO3 (D) HCl

Assertion Reason:
(A) If both statement-I and statement-II are true
and statement II is the correct explanation of
Statement I.
(B) If both statement-I and statement-II are true
and statement II is not the correct explanation
of Statement I.
(C) If statement-I is true but Statement-II is
false.
(D) If statement-I is false and statement-II is
true.
Q.33 Statement-I: HClO4 is only oxidising
agent.
Statement-II: Cl is most electro-negative
element in H, Cl and O.

Q.34 Statement-I: In FeS2 oxidation Number


of iron is +4.
Statement-II: In FeS2 (S  S ) linkage is
present.

Q.35 Statement-I: In given reaction H2 O 2 is


oxidising & reducing agent
1
H2O2  H2O  O2
2
Statement-II: In H2 O 2 is a bleaching reagent.

Q.36 Statement-I: In basic medium colour of


K 2Cr2O7 is changed from orange to yellow.
Statement-II: In basic medium K 2Cr2O7 is
changed in chromate ion.
 
Q.37Statement-I: I2 IO3  I .
This reaction is disproportionate reaction.
Statement-II: Oxidation number of I can vary
from –1 to +7.

1.9
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Stoichiometry and Redox Reactions

PREVIOUS YEARS QUESTIONS JEE MAIN

MOLE CONCEPT
(A) MW/2 (B) MW/3
(C) MW/6 (D) MW/1
Q.1 If we consider that 1/6, in place of 1/12,
mass of carbon atom is taken to be the relative
atomic mass unit, the mass of one mole of a REDOX REACTION
substance will (AIEEE 2002)
(A) Decrease twice Q.7 Several blocks of magnesium are fixed to
(B) Increase two fold the bottom of a ship to (AIEEE 2003)
(C) Remain unchanged (A) Keep away the sharks
(D) Be a function of the molecular mass of the (B) Make the ship lighter
substance (C) Prevent action of water and salt
(D) Prevent puncturing by under-sea rocks
Q.2 A molar solution is one that contains one
mole of a solute in (IIT JEE 1986) Q.8 Which of the following chemical reactions
(A) 1000 g of the solvent depicts the oxidizing behaviour of H2SO4 ?
(B) One litre of the solvent (AIEEE 2006)
(C) One litre of the solution (A) 2HI  H2SO4  I2  SO2  2H2O
(D) 22.4 litres of the solution
(B) Ca(OH) 2  H2SO4  CaSO4  2H2O
Q.3 In the reaction, (AIEEE 2007) (C) NaCl  H2SO4  NaHSO4  HCl
3
2Al(s)  6HCl(S)  2Al (aq)  6Cl  (aq)  3H 2 (g) (D) 2PCl5  H2SO4 
(A) 6L HCl (aq) is consumed for every 3L H2(g) 2POCl3  2HCl  SO2Cl2
produced
(B) 33.6L H2(g) is produced regardless of Q.9 The oxidation number of carbon in CH2O
temperature and pressure for every mole Al is (IIT JEE 1982; EAMCET 1985; MNR 190; CPMT
that reacts 1997, 2004; UPSEAT 2001; RPMT 2006; Gujarat
(C) 67.2L H2(g) at STP is produced for every CET 2007)
mole Al that racts (A) –2 (B) +2 (C) 0 (D) 4
(D) 11.2 H2(g) at STP is produced for every
mole HCl (aq) consumed Q.10 The oxidation state of chromium in the
final product formed by the reaction between
Q.4 How many moles of magnesium KI and acidified potassium dichromate solution
phosphate, Mg3 (PO4 ) 2 will contain 0.25 mole of is (AIEEE 2005)
oxygen atoms (AIEEE 2006) (A) +4 (B) +6 (C) +2 (D) +3
(A) 0.02 (B) 3.125 10 2 Q.11 When KMnO4 acts as an oxidising agent
(C) 1.25  10 2 (D) 2.5  10
2
and ultimately forms [MnO4 ]2 , MnO2 , Mn2O3 ,
Q.5 If 1021 molecules are removed from 200 mg
Mn2 then the number of electrons transferred
of CO2 , then the number of moles of CO2 left in each case respectively is
are (IIT JEE 1983) (AIEEE 2002)
3
(A) 2.85  10 (B) 28.8  103 (A) 4, 3, 1, 5 (B) 1, 5, 3, 7
(C) 0.288  10 3 (D) 1.68  10
2 (C) 1, 3, 4, 5 (D) 3, 5, 7, 1

Q.6 In standardization of Na 2S2O3 using Q.12 Which of the following is a redox reaction
(AIEEE 2002)
K 2Cr2O7 by iodometry, the equivalent weight
(A) NaCl  KNO3  NaNO3  KCl
of K 2Cr2O7 is (IIT JEE 2000)
(B) CaC2O4  2HCl  CaCl2  H2C2O4

1.10
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Stoichiometry and Redox Reactions

(C) Mg(OH)2  2NH4Cl 


MgCl2  2NH4OH
(D) Zn  2AgCN  2Ag  Zn(CN) 2


Q.13 The product of oxidation of I and MnO4
in alkaline medium is (IIT Screening 2004)
(A) IO 3 (B) I2

(C) IO (D) IO 4
Q.14 For H3PO3 and H3PO4 the correct choice
is (IIT Screening 2003)
(A) H3PO3 is dibasic and reducing
(B) H3PO3 is dibasic and non-reducing
(C) H3PO4 is tribasic and reducing
(D) H3PO3 is tribasic and non-reducing

1.11
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Stoichiometry and Redox Reactions

EXERCISE-1 JEE ADVANCED


MOLE CONCEPT Q.8 200 ml of a solution of mixture of NaOH
and Na 2 CO3 was first titrated with
Q.1 How many gm of HCl is needed for phenolphthalein and N/10 HCl. 17.5 mL of HCl
complete reaction with 69.6 gm MnO2 ? was required for the end point. After this
HCl  MnO2  MnCl2  H2O  Cl2 methyl orange was added and 2.5 mL of same
HCl was again required for next end point. Find
Q.2 Titanium, which is used to make air plane out amount of NaOH and Na 2 CO3 in mixture.
engines and frames, can be obtained from
titanium tetrachloride, which is turn is obtained
Q.9 Potassium superoxide, KO 2 , is used in
from titanium oxide by the following process: rebreathing gas masks to generate oxygen:
3TiO2 (s)  4C(s)  6Cl2 (g)  KO2 (s)  H2O(l )  KOH(s)  O 2 (g)
3TiCl4 (g)  2CO2 (g)  2CO(g) If a reaction vessel contains 0.158 mol KO 2 and
A vessel contains 4.32 g TiO2 , 5.76 g C and 6.82 0.10 mol H2 O , how many moles of O2 can be
g Cl2 , suppose the reaction goes to completion produced?
as written, how many gram of TiCl4 can be Q.10 A sample of mixture of CaCl2 and NaCl
produced? (Ti = 48). weighing 4.22 gm was treated to precipitate all
Q.3 Sulphuric acid is produced when sulphur the Ca as CaCO3 which was then heated and
dioxide reacts with oxygen and water in the quantitatively converted to 0.959 gm of CaO.
presence of a catalyst: Calculate the percentage of CaCl2 in the
2SO2 (g)  O 2 (g)  2H2O(l )  2H2SO 4 . If 5.6 mixture.
mol of SO2 reacts with 4.8 mole of O2 and a
Q.11 Cyclohexanol is dehyrated to
large excess of water, what is the maximum cyclohexene on heating with conc. H2SO4 . If
number f moles of H2SO4 that can be
the yield of this reaction is 75%, how much
obtained? cyclohexene will be obtained from 100 g of
con.H SO
Q.4 What weight of Na 2CO3 of 95% purity cyclohexanol? C6H12O 
2 4
C6H10
would be required to neutralize 45.6 mL of
Q.12 How many grams of 90% pure Na 2SO4
0.235 N acid?
can be produced from 250 gm of 95% pure
Q.5 How much BaCl2 .2H2O and pure water to NaCl?
be mixed to prepare 50g of 12.0% (by wt.)
Q.13 A precipitate of AgCl and AgBr weighs
BaCl2 solution.
0.4066 g. On heating in a current of chlorine,
Q.6 To 50 litre of 0.2 N NaOH, 5 litre of 1N HCl the AgBr is converted to AgCl and the mixture
and 15 litre of 0.1 N FeCl3 solution are added. loses 0.0725 g in weight. Find the percentage
of Cl in original mixture.
What weight of Fe 2O3 can be obtained from
the precipitate? Also report the normality of Q.14 How many milli-litre of 0.5 M H2SO4 are
NaOH left in the resultant solution. needed to dissolve 0.5 g of copper II
carbonate?
Q.7 0.5 g fuming H2SO4 (oleum) is diluted with
water. The solution requires 26.7 mL of 0.4 N Q.15 What is the strength in g per litre of a
NaOH for complete neutralization. Find the solution of H2SO4 , 12 mL of which neutralized
percentage of free SO3 in the sample of oleum. 15 mL of N/10 NaOH solution.

1.12
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Stoichiometry and Redox Reactions

Q.16 n-butane is produced by the solution distilled. The ammonia released was
monobromination of ethane followed by Wurtz then trapped in 10 Meq of second acid
reaction. Calculate the volume of ethane at NTP solution. Back titration of this solution required
required to produce 55 g n-butane if the 6 Meq of the base. Calculate the percentage of
bromination takes place with 90% yield and the Mg burnt to the nitride.
Wurtz reaction with 85% yield.
Q.22 A mixture of ethane (C 2H6 ) and ethene
Q.17 0.50 g of a mixture of K 2CO3 and Li2CO3 (C 2H4 ) occupies 40 litre at 1.00 atm and at 400
required 30 mL of 0.25 N HCl solution for K. The mixture reacts completely with 130 g of
neutralization. What is percentage composition O2 to produce CO2 and H2 O . Assuming ideal
of mixture?
gas behaviour, calculate the mole fractions of
Q.18 Sodium chlorate, NaClO3 , can be C2H4 and C2H6 in the mixture.
prepared by the following series of reactions:
Q.23 A solid mixture 5 g consists of lead nitrate
2KMnO4  16HCl  2KCl  2MnCl2  8H2O  5Cl2 and sodium nitrate was heated below 600ºC
6Cl2  6Ca(OH)2  Ca(ClO3 )2  5CaCl2  6H2O until weight of residue was constant. If the loss
in weight is 28%, find the amount of lead nitrate
Ca(ClO3 )2  Na2SO4  CaSO4  2NaClO3 and sodium nitrate in mixture.
What mass of NaClO3 can be prepared from Q.24 Upon mixing 45.0 mL of 0.25 M lead
100 ml of concentrated HCl (density 1.18 nitrate solution with 25 mL of 0.10 M chromic
gm/ml and 36% by mass)? Assume all other sulphate, precipitation of lead sulphate takes
substance are present in excess amounts. place. How many moles of lead sulphate are
formed? Also calculate the molar concentration
Q.19 In a determination of P an aqueous
of the species left behind in final solution.
solution of NaH2PO4 is treated with a mixture
Assume that lead sulphate is completely
of ammonium and magnesium ions to precipitate insoluble.
magnesium ammonium phosphate
Mg(NH4 )PO4 .6H2O . This is heated and Q.25 A 10 g sample of a mixture of calcium
decomposed to magnesium pyrophosphate, chloride and sodium chloride is treated with
Mg2P2O7 which is weighed. A solution of Na 2CO3 to precipitate calcium as calcium
NaH2PO4 yielded 1.054 g of Mg2P2O7 . What carbonate. This CaCO3 is heated to convert all

weight of NaH2PO4 was present originally? the calcium to CaO and the final mass of CaO is
1.12 gm. Calculate % by mass of NaCl in the
Q.20 5 mL of 8 N HNO3 , 4.8 mL of 5 N HCl and original mixture.
a certain volume of 17 M H2SO4 are mixed Q.26 A mixture of Ferric oxide (Fe 2O3 ) and Al
together and made upto 2 litre. 30 mL of this is used as solid rocket fuel which reacts to give
acid mixture exactly neutralizes 42.9 mL of Al2O3 and Fe. No other reactants and products
Na 2CO3 solution containing 1 g
are involved. On complete reaction of 1 mole
Na 2CO3 .10H2O in 100 mL of water. Calculate of Fe 2O3 , 200 units of energy is released.
the amount of sulphate ions in g present in (i) Write a balance reaction representing the
solution. above change.
(ii) What should be the ratio of masses of
Q.21 A sample of Mg was burnt in air to give a
mixture of MgO and Mg3N2 . The ash was
Fe 2O3 and Al taken so that maximum energy
per unit mass of fuel is released.
dissolved in 60 Meq of HCl and the resulting
(iii) What would be energy released if 16 kg of
solution was back titrated with NaOH. 12 Meq
of NaOH were required to reach the end point.
Fe 2O3 reacts with 2.7 kg of Al.
As excess of NaOH was then added and the

1.13
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Stoichiometry and Redox Reactions

Q.27 A mixture of nitrogen and hydrogen. In Q.31 124 gm of mixture containing NaHCO3 ,
the ratio of one mole of nitrogen to three moles AlCl3 , & KNO3 requires 500 ml, 8% w/w NaOH
of hydrogen, was partially converted into NH3
solution [ dNaOH = 1.8 gm/ml] for complete
so that the final product was a mixture of all
neutralisation. On heating same amount of
these three gases. The mixture was to have a
mixture, it known loss in weight of 18.6 gm.
density of 0.497 g per litre at 25ºC and 1.00
Calculate % composition of mixture by moles.
atm. What would be the mass of gas in 22.4
Weak base formed doesn't interfere in reaction.
litres at 1 atm and 273 K? Calculate the %
Assume KNO3 does not decompose under
composition of this gaseous mixture by
volume. given conditions.

Q.28 In one process for waterproofing, a fabric Q.32 If the yield of chloroform obtainable from
is exposed to (CH3 ) 2 SiCl2 vapour. The vapour acetone and bleaching powder is 75%. What is
the weight of acetone required for producing
reacts with hydroxyl groups on the surface of
30 gm of chloroform?
the fabric or with traces of water to form the
waterproofing film [(CH3 ) 2 SiO]n , by the Q.33 A sample of impure Cu2O contains
reaction 66.67% of Cu. What is the percentage of pure
 
n(CH3 ) 2 SiCl2  2nOH  2nCl  nH2O  [(CH3 ) 2 SiO]
Cun2O in the sample?
where n stands for a large integer. The
Q.34 Equal weights of mercury and iodine are
waterproofing film is deposited on the fabric
allowed to react completely to form a mixture
layer upon layer. Each layer is 6.0 Å thick [the
of mercurous and mercuric iodide leaving none
thickness of the (CH3 ) 2 SiO group]. How much
of the reactants. Calculate the ratio by weight
(CH3 )2 SiCl2 is needed to waterproof one side of Hg 2I2 and HgI2 and formed. (Hg = 200, I =
of a piece of fabric, 1.00 m by 3.00 m, with a 127)
film 300 layers thick? The density of the film is
1.0 g/cm3.

Q.29 Two substance P4 and O2 are allowed to


react completely to form mixture of P4 O6 &
P4O10 leaving none of the reactants. Using this
information calculate the composition of final
mixture when mentioned amount of P4 & O2
are taken.
P4  3O2 P4O6
P4  5O2 P4O10
(i) If 1 mole P4 & 4 mole of O2
(ii) If 3 mole P4 & 11 mole of O2
(iii) If 3 mole P4 & 13 mole of O2

Q.30 Chloride samples are prepared for


analysis by using NaCl, KCl and NH4Cl
seperately or as mixture. What minimum
volume of 5% by weight AgNO3 solution (sp.
gr., 1.04 g ml–1) must be added to a sample of
0.3 g in order to ensure complete precipitation
of chloride in every possible case?

1.14
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Stoichiometry and Redox Reactions

REDOX REACTION
Q.9 20 mL of 0.2 M MnSO4 are completely
Q.1 Indicate the oxidation of underlined in each oxidized by 16 mL of KMnO4 of unknown
case: 4
normality, each forming Mn oxidation state.
(a) NaNO2 (b) H2
Find out the normality and molarity of KMnO4
(c) Cl2O7 (d) KCr O3Cl
solution.
(e) BaCl2 (f) ICl3
Q.10 KMnO4 solution is to be standardized by
(g) K 2 Cr 2O7 (h) CH2O
titration against As2O3 (s). A 0.1097 g sample
(i) Ni(CO) 4 (j) NH2OH
of As 2O3 requires 26.10 mL of the KMnO4
Q.2 Indicate the each reaction which of the solution for its titration. What are the molarity
reactant is oxidized or reduced if any: and normality of the KMnO4 solution?
(a) CuSO4  4KI  2CuI  I2  2K 2SO4
Q.11 0.518 g sample of limestone is dissolved
(b) and then Ca is precipitated as CaC2O4 . After
2Na 2S  4HCl  SO2  4NaCl  3S  2H2O filtering and washing the precipitate, it requires

(c) NH4NO2 
N2  2H2O 40 mL of 0.25 N KMnO4 solution to equivalence
point. What is percentage of CaO in limestone?
Q.3 Calculate the number of electrons lost or
gained during the changes: Q.12 20 mL of a solution containing 0.2 g of
(a) 3Fe  4H2O Fe 3 O4  4H2 impure sample of H2 O 2 reacts with 0.316 g of
KMnO4 (acidic). Calculate:
(b) AlCl3  3K  Al  3KCl
(i) Purity of H2 O 2 ,
Q.4 Explain, why? (ii) Volume of dry O2 evolved at 27ºC and 750
(a) H2S acts as reductant whereas, SO2 acts as mm P.
reductant and oxidant both.
(b) H2 O 2 acts are reductant and oxidant both. Q.13 5.7 g of bleaching powder was
suspended in 500 mL of water 25 mL of this
Q.5 MnO4 can oxidize NO2 to NO3 in basic suspended on treatment with KI and HCl

liberated iodine which reacted with 24.35 mL
medium. How many mol of NO2 are oxidized of N/10 Na 2S2O3 . Calculate percentage of

by 1 mol of MnO4 ? available Cl2 in bleaching powder.

Q.6 Which is stronger base in each pair? Q.14 Balance the following equation:
(a) HSO4 ;HSO; (b) NO2 ;NO3 ; (i) C2H5 OH  K 2Cr2O7  H2SO4 
(c)

Cl ; ClO C2H4O2  Cr2 (SO4 )3  K 2SO4  H2O
(ii) As 2S5  HNO3 
Q.7 Fill in the blanks and balance the
NO2  H2O  H3 AsO4  H2SO4
following equations:
(a) Zn + HNO3  ........... + N2O  ............ (iii) CrI3  Cl3  KOH 
(b) HI  HNO3  ..........  NO  H2O KIO4  K 2CrO4  KCl  H2O
(iv) As 2 S3  HClO3  H2O 
Q.8 What volume of 0.20 M H2SO4 is
HCl  H3 AsO4  H2SO4
required to produce 34.0 g of H2S by the
reaction: Q.15 Balance the following equations:
8KI  5H2SO4  4K 2SO4  4I2  H2S  4H2O

1.15
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Stoichiometry and Redox Reactions

(i) was removed by boiling. The total chloride was



As2S3  OH  H2O2  AsO42  SO42  H2O precipitated as silver chloride. The weight of
precipitate was 0.1435 g. In another
experiment, 25 mL of original solution was
heated with 30 mL of 0.2 N ferrous sulphate
(ii)
solution and unreacted ferrous sulphate
CrI3  H2O2  OH  CrO42  3IO4  H2O required 37.5 mL of 0.08 N solution of an
 
(iii) P4  OH  H2O2 H2PO2  PH3 oxidant for complete oxidation. Calculate the
(iv) molar ratio of chlorate to chloride in the given
 H2O
As 2S3  NO3  H  H3 AsO4  NO  S mixture. Fe 2 reacts with ClO3 according to
equation.
Q.16 Mg can reduce NO3 to NH3 in basic ClO3  6Fe 2  6H  Cl  6Fe 3  3H2O
solution:
Q.20 (i) CuSO4 reacts with KI in acidic medium
NO3  Mg(s)  H2O 
to liberate I2
Mg(OH)2 (s)  OH (aq)  NH3 (g)
 2CuSO4  4KI  Cu2I2  2K 2SO4  I2
A 25.0 mL sample of NO3 solution was treated
(ii) Mercuric per iodiate Hg5 (IO6 ) 2 reacts with a
with Mg. The NH3 (g) was passed into 50 mL of
mixture of KI and HCl following the equation:
0.15 N HCl. The excess HCl required 32.10 mL
Hg5 (IO6 ) 2  34KI  24HCl 
of 0.10 M NaOH for its neutralization. What was
NO3
5K 2HgI4  8I2  24KCl  12H2O
the molarity of ions in the original sample.
(iii) The liberated iodine is titrated against
Q.17 An acid solution of KReO4 sample Na 2S2O3 solution. One mL of which is
containing 26.83 mg of combined rhenium was equivalent to 0.0499 g of CuSO4 .5H2O . What
reduced by passage through a column of volume in mL of Na 2S2O3 solution will be
granulated zinc. The effluent solution including required to react with I2 liberated from 0.7245
the washing from the column, was then titrated
g of Hg5 (IO6 ) 2 ? M. wt. of Hg5 (IO6 ) 2 = 1448.5
with 0.05 N KMnO4 . 11.45 mL of the standard
and M. wt. of CuSO4 .5H2O = 249.5.
KMnO4 was required for the reoxidation of all
the rhenium to the perrhenate ion ReO 4 . Q.21 1.249 g of a sample of pure BaCO3 and
Assuming that rhenium was the only element impure CaCO3 containing some CaO was
reduced, what is the oxidation state to which treated with dil. HCl and it evolved 168 mL of
rhenium was reduced by the zinc column. CO2 at NTP. From this solution BaCrO4 was
Q.18 100 mL solution of FeC2O4 and FeSO4 is precipitated, filtered an washed. The dry
completely oxidized by 60 mL of 0.02 M precipitate was dissolved in dilute H2SO4 and
KMnO4 in acid medium. The resulting solution dilute to 100 mL. 10 mL of this solution when
is then reduced by Zn and dil.HCl. The reduced treated with KI solution liberated iodine which
solution is again oxidized completely by 40 mL required exactly 20 mL of 0.05 N Na 2S2O3 .
of 0.02 M KMnO4 . Calculate normality of Calculate percentage of CaO in the sample.
FeC2O4 and FeSO4 in mixture. Q.22 A 10 g mixture of Cu2S and CuS was

Q.19 1 g of most sample of KCl and KClO3 was treated with 200 mL of 0.75 M MnO4 in acid
dissolved in water to make 250 mL solution, 25 solution producing SO2 , Cu2 Mn2 . The
and
mL of this solution was treated with SO2 to 
SO2 was boiled off and the excess of MnO4
reduce chlorate to chloride and excess of SO2

1.16
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Stoichiometry and Redox Reactions
2 reduced by 30 mL of 0.1 N FeSO4 solution.
was treated with 175 mL of 1 M Fe solution.
Calculate percentage of CuS in original mixture. Calculate the amount of MnSO4 .4H2O in
Q.23 For estimating ozone in the air, a certain sample.
volume of air is passed through an acidified or Q.28 Write complete balanced equation for
neutral KI solution when oxygen is evolved and the following in acidic medium by ion-electron
iodide is oxidised to give iodine. When such a method:
solution is acidified, free iodine is evolved
(a) ClO3  Fe 2  Cl  Fe 3  H2O
which can be titrated with standard Na 2S2O3
 2
solution. In a experiment 10 litre of air at 1 atm (b) CuS  NO3  Cu  S8  NO  H2O
2
and 27ºC were passed through an alkaline Ki (c) S2O3  Sb 2O3  SbO  H2SO3
solution, at the end, the iodine entrapped in a
(d) HCl  KMnO4  Cl2  KCl  MnCl2  H2O
solution on titration as above required 1.5 mL
of 0.01 N Na 2S2O3 solution. Calculate volume (e)
percentage of O3 in sample. KClO3  H2SO4 KHSO4  HClO4  ClO3  H2O
(f) HNO3  HBr NO  Br2  H2 O
Q.24 30 ml of an acidified solution of 1.5 N   
(g) IO4  I  H I2  H2O
MnO4 ions, 15 mL of 0.5 N oxalic acid and 15
mL of 0.4 N ferrous salt solution are added Q.29 Balance the following equations by
together. Find the molarities of MnO4 
and Fe 3 oxidation method:
ions in the final solution? (a) Cu  NO3  ......  Cu2  NO2  .....
(Acid medium)
Q.25 (i) 25 mL of H2 O 2 solution were added to 
excess of acidified solution of KI. The iodine so
(b) CI2  IO3

 OH IO4  .........  H2O
liberated required 20 mL of 0.1 N Na 2S2O3 for (Basic medium)
titration. Calculate the strength of H2 O 2 in (c) H2S  K 2CrO4  H2SO4 ......
terms of normality, percentage and volume. (Acid medium)
2
(ii) To a 25 mL H2 O 2 solution, excess of (d) Fe  MnO4 Fe 3  Mn2  ....
acidified solution of KI was added. The iodine (Acid medium)
liberated required 20 mL of 0.3 N sodium (e) KMnO4  H2SO4  H2O2 
thiosulphate solution. Calculate the volume
K 2SO4  MnSO4  H2O  .......
strength of H2 O 2 solution.
(Acid medium)
Q.26 An aqueous solution containing 0.10 g (f) MnO2  H2O2 MnO4  H2O
KIO3 (formula weight = 214.0) was treated with (Basic medium)
an excess of KI solution. The solution was
acidified with HCl. The liberated I2 consumed Q.30 Write complete balance equation for the
following in basic medium by ion-electron
45 mL of thiosulphate solution to decolorise
method:
the blue starch-iodine complex. Calculate the
molarity of the sodium thiosulphate solution. (a) S2O42  Ag2O  Ag  SO32
  
(b) Cl2  OH  Cl  ClO
Q.27 A sample of MnSO4 .4H2O is strongly   
heated in air. The residue (Mn3 O4 ) left was (c) H2  ReO4  ClO2  Sb(OH)6
  
dissolved in 100 mL of 0.1 N FeSO 4 containing (e) I2  OH  I  IO3
 2 2 3
dil. H2SO4 . This solution was completely (f) MnO4  Fe  Mn  Fe
reacted with 50 mL of KMnO4 solution. 25 mL
of this KMnO4 solution was completely

1.17
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Stoichiometry and Redox Reactions

EXERCISE-2 JEE ADVANCED


MOLE CONCEPTQ.1 'x' gms of an (I) NH3  O2  NO  H2O
element 'A' on heating in a jar of chlorine give (II) NO  O2  NO2
'y' gms of ACl2 the atomic weight of element (III) NO2  H2O  HNO3  HNO2
A is (IV) HNO2  HNO3  NO  H2O
 x  35.5 71x Select the correct option(s):
(A)  y  71   2 (B)
y  71 (A) Moles of HNO3 obtained is half of moles of
 
35.5x Ammonia used if HNO2 is not used to produce
(C) (D) None of these
y  71 HNO3 by equation (IV)
(B) 100/6% more HNO3 will be produced if
Q.2 The amount of H2SO4 present in 1200 ml
HNO2 is used to produce HNO3 by reaction
of 0.2 N solution is
(IV) than if HNO2 is not used to produce HNO3
(A) 10.76 gms (B) 11.76 gms
(C) 12.76 gms (D) 14.76 gms by reaction (IV)
(C) If HNO2 is used to produce HNO3 then
Q.3 An iodized salt contains 0.5% of NaI. A
1/4th of total HNO3 is produced by reaction
person consumes 3 gm of salt everyday. The
number of iodide ions going into his body (IV)
everyday is (D) Moles of NO produced in reaction (IV) is
50% of moles of total HNO3 produced.
(A) 104 (B) 6.02  104
(C) 6.02  10 (D) 6.02  10
19 23
Comprehension:
Normality is number of gram equivalents
Assertion Reason:
dissolved per litre of solution. It changes with
(A) If both statement-I and statement-II are true
change in temperature. In case of monobasic
and statement II is the correct explanation of
acid, normality and molarity are equal but in
Statement I, the mark (A).
case of dibasic acid, normality is twice the
(B) If both statement-I and statement-II are true
molarity. In neutralization and redox reactions,
and statement II is not the correct explanation
number of mill equivalents of reactants as well
of Statement I, the mark (B).
as products are always equal.
(C) If statement-I is true but Statement-II is
false, then mark (C). Q.7 On heating a litre of a N/2 HCl solution,
(D) If both statement-I and statement-II are 2.750 g of HCl is lost and the volume of solution
false, then mark (D). becomes 750 mL. The normality of resulting
solution will be
Q.4 Statement-I: 0.28 g of N2 has equal volume
(A) 0.58 (B) 0.75 (C) 0.057 (D) 5.7
as 0.44 g of another gas at same conditions of
temperature and pressure. Q.8 The volume of 0.1 M Ca(OH) required to
Statement-II: Molecular mass of another gas is neutralize 10 mL of 0.1 N HCl will be
44 g mol–1. (A) 10 mL (B) 20 mL (C) 5 mL (D) 40 mL

Q.5 Statement-I: Boron has relative atomic Q.9 Molarity of 0.5 N Na 2CO3 is
mass 10.81. (A) 0.25 (B) 1.0 (C) 0.5 (D) 0.125
10
Statement-II: Borons two isotopes, 5 B and
Q.10 6.90 N KOH solution in water contains
11
5 B and their relative abundance is 19% and 30% by weight of KOH. The density of solution
81%. will be
(A) 1.288 (B) 2.88 (C) 0.1288 (D) 12.88
Q.6 Given following series of reactions:

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Stoichiometry and Redox Reactions

Q.11 The amount of ferrous ammonium (C) O (R) 44.95%


sulphate required to prepare 250 mL of 0.1 N
Q.15 The recommended daily does is 17.6
solution is
milligrams of vitamin C (ascorbic acid) having
(A) 1.96 g (B) 1.8 g (C) 9.8 g (D) 0.196 g
formula C6H8 O6 . Match the following. Given:
Q.12A 4.925 g sample of a mixture of CuCl2 NA  6  10 23
and CuBr2 was dissolved in water and mixed
Column-I Column-II
thoroughly with a 5.74 g portion of AgCl. After (A) O-atoms present 4
(P) 10 mole
the reaction and solid, a mixture of AgCl and
AgBr, was filtered, washed, and dried. Its mass (B) Moles of vitamin C (Q) 5.68  10 3
was found to be 6.63 g. in 1 gm of vitamin C
(A) % By mass of CuBr2 in original mixture is (C) Moles of vitamin C (R) 3.6  10 20
(A) 2.24 (B) 74.5 (C) 45.3 (D) None in 1 gm should be
(B) % By mass of Cu in original mixture is consumed daily
(A) 38.68 (B) 19.05 (C) 3.86 (D) None Q.16 If volume strength of H2 O 2 solution is 'X-
(C) % by mole of AgBr in dried precipitate is
V' then its
(A) 25 (B) 50 (C) 75 (D) 60
 Column-I Column-II
(D) No. of moles of Cl ion present in the X
solution after precipitate ion are (A) Strength in g/L (i)
(A) 0.06 (B) 0.02 (C) 0.04 (D) None 11.2
X
Q.13 Water is added to 3.52 grams of UF6 . The (B) Volume strenght X (ii)
5.6
products are 3.08 grams of a solid [containing 17X
only U, O and F] and 0.8 gram of a gas only. The (C) Molarity (iii)
5.6
gas [containing fluorine and hydrogen only],
(D) Normality (iv) 5.6 × N
contains 95% by mass fluorine.
(A) (A)-(iii), (B)-(i), (C)-(iv), (D)-(ii)
[Assume that the empirical formula is same as
(B) (A)-(iv), (B)-(i), (C)-(ii), (D)-(i)
molecular formula.]
(C) (A)-(iii), (B)-(iv), (C)-(i), (D)-(ii)
(A) The empirical formula of the gas is
(D) (A)-(iii), (B)-(ii), (C)-(iv), (D)-(i)
(A) HF2 (B) H2F (C) HF (D) HF3
Q.17
(B) The empirical formula of the solid product Column-I Column-II
is x  d  10
(A) MR on mixing two
(A) UF2O2 (B) UFO2 (C) UF2 O (D) UFO (i)
acidic solutions Msolute
(C) The percentage of fluorine of the original (B) MR on mixing two basic
compound which is converted into gaseous (ii) n × M × V ml
solutions
compound is
(C) MR on mixing two M1V1  M 2 V2
(A) 66.66% (B) 33.33% (C) 50% (D) 89.9% (iii)
acidic and basic solutions V1  V2
Match the column:
M1V1
Q.14 One type of artificial diamond (commonly (D) milliequivalent (iv)
called YAG for yttrium aluminium garnet) can V2
be represented by the formula Y3 Al5 O12 . [Y = M1V1  M 2 V2
(E) Molarity (v)
89, Al = 27] V1  V2
(A) (A)-(i), (B)-(iii), (C)-(i), (D)-(ii), (E)-(iv)
Column-I Column-II
(B) (A)-(v), (B)-(v), (C)-(iii), (D)-(ii), (E)-(i, iv)
(A) Y (P) 22.73% (C) (A)-(ii), (B)-(i), (C)-(ii), (D)-(iii), (E)-(ii)
(B) Al (Q) 32.32% (D) (A)-(i), (B)-(ii), (C)-(ii), (D)-(iii), (E)-(iii)

1.19
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Stoichiometry and Redox Reactions

REDOX REACTIONS
Q.1 One mole of N2H4 loses ten moles of suitable conditions. Titrations involve the direct
electrons to form a new compound Y. use of iodine as oxidising agent are known as
Assuming that all the nitrogen appears in the iodimetric titrations while those titrations
new compound, what is the oxidation state of involving indirect use of iodine are known as
nitrogen in Y? (There is no change in the iodometric titrations. These titrations are used
oxidation state of hydrogen) for the estimation of oxidising agents like
(A) –1 (B) –3 (C) +3 (D) +5 KMnO4 , K 2Cr2O7 , CuSO4 etc.
Q.2 Which is best reducing agent Q.9 50 ml of an aqueous solution of H2 O 2 was
   
(A) F (B) Cl (C) Br (D) I treated with excess of KI solution and the
iodine so liberated quantitatively required 20
Q.3 In the alumino thermite process, aluminium ml of 0.1 N solution of hypo. This titration is
acts as known as:
(A) an oxidizing agent (B) a flux (A) iodometric titration
(C) reducing agent (D) a solder (B) iodimetric titration
Q.4 Zinc-copper couple that can be used as a (C) potassium iodide titration
reducing agent is obtained by (D) all of these
(A) mixing zinc dust and copper gas Q.10 In the above problem, concentration of
(B) zinc coated with copper H2O2 in gm/litre is:
(C) copper coated with zinc
(A) 6.8 (B) 0.68 (C) 0.068 (D) 0.34
(D) zinc and copper wires welded together
Q.11 0.5 gm sample of pyrolusite (MnO2 ) is
Q.5 In the following equations value of X is
treated with HCl, the Cl2 gas evolved is treated
ClO3  6H  X  Cl  3H2O
with KI, the violet vapours evolved are
(A) 4e  (B) 5e  (C) 6e  (D) 7e  absorbed in 30 ml 0.1 N Na 2S2O3 solution
Q.6 The brown ring complex compound is percentage purity of pyrolusite sample is
 (A) 30% (B) 50% (C) 36% (D) 26.1%
formulated as [Fe(H2O)5 (NO) ]SO4 . The
oxidation state of iron is Q.12 Arsenite gets converted into arsenate by
(A) 1 (B) 2 (C) 3 (D) 0 using iodine, valency factor for Arsenite and
Iodine are respectively
Q.7 Oxidation state of oxygen atom in
(A) 2 and 2 (B) 2 and 1 (C) 1 and 2 (D) 5 and 2
potassium superoxide is
(A) –1/2 (B) –1 (C) –2 (D) 0 Oxidation and reduction process involves the
transaction of electrons. Loss of electrons is
Q.8 In the following reaction
oxidation and the gain of electrons is reduction.
3Br2  6CO32  3H2O  It is thus obvious that in a redox reaction, the
5Br   6HCO3  BrO3 oxidant is reduced by accepting the electrons
and the reductant is oxidised by losing
(A) bromine is both reduced and oxidised
electrons. The reactions in which a species
(B) bromine is neither reduced and oxidised
disproportionate into two oxidation states
(C) bromine is oxidised and carbonate is
(lower and higher) are called
reduced
disproportionation reactions. In
(D) bromine is reduced and water is oxidised
electrochemical cells, redox reaction is
Comprehension involved, i.e., oxidation takes place at anode
The redox titration involve the chemical and reduction at cathode.
reaction between the oxidising agent and
reducing agent in aqueous solutions under Q.13 The reaction: Cl2  Cl  ClO3 is

1.20
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Stoichiometry and Redox Reactions

(A) oxidation (B) reduction Q.18 Statement-I: In PbO4 all Pb has +8/3
(C) disproportionation oxidation number.
(D) neither oxidation nor reduction Statement-II: Pb 3 O4 is mixed oxide of PbO &
Q.14 In the reaction: PbO2 .
I2  2S2O32  2I 
 S4O62 Q.19 Column Matching:
(A) I2 is reducing agent Column-I Column-II
(1)Increase in oxidation (a)Loss of electrons
(B) I2 is oxidising agent
number
(C) S 2 O32 is reducing agent (2)Decrease in oxidation (b)Redox reaction
(D) S 2 O3
2
is oxidising agent number
(3)Oxidising agent (c)Fractional
Q.15 Determine the change in oxidation oxidation number
number of sulphur is H2S and SO2 respectively (4)Reducing agent (d)Zero oxidation
in the following reaction: number
2H2S  SO2  2H2O  3S (5) 2Cu  Cu +Cu
+ 2+ (e) Simple
neutralisation
(A) 0, +2 (B) +2, –4 (C) –2, +2 (D) +4, 0
reaction
Q.16 Which of the following reactions is/are (6) MnO2  4HCl (f)Gain of electrons
correctly indicated?  MnCl + Cl2 + 2H2O
2
Oxidant Reductant (7) Mn3 O4 (g) Disproportion-
(A) HNO3  Cu  Cu2  NO2 ation
(B) 2Zn  O2  ZnO (8) CH2Cl2 (h) Oxidation
  (9)NaOH + HCl (i) Reduction
(C) Cl2  2Br  2Cl  Br2
 NaCl  H2O
(D) 4Cl2  CH4  CCl4  4HCl

Assertion and Reason Q.20 Match the reactions in column I with


Each of the questions given below consist of nature of the reactions/type of the products in
Statement-I and Statement-II. Use the Column II.
following Key to choose the appropriate Column-I Column-II
answer.
(A) If both Statement-I and Statement-II are
(A) O2  O2  O2 2 (P) redox reaction

true, and Statement-II is the correct (B) CrO4 2  H  (Q) one of the
explanation of Statement-I. products has
(B) If both Statement-I and Statement-II are trigonal planar
true, and Statement-II is not the correct structure
explanation of Statement-I. (C) (R) dimeric
(C) If Statement-I is true but Statement-II is
false.
MnO4  NO2 
H  bridged
tetrahedral metal
(D) If Statement-I is false but Statement-II is ion
true.
(D) (S)
Q.17 Statement-I: In CrO5 oxidation number of NO3  H2SO4  Fe 2  disproportionatio
n
Cr is +6.
Statement-II: CrO5 has butterfly structure in
O
O O
Cr
which peroxide bonds are present. O O

1.21
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Stoichiometry and Redox Reactions

PREVIOUS YEARS QUESTIONS JEE ADVANCED


Q.1 Naturally occurring boron consists of two (C) (molecular weight)/3
isotopes whose atomic weights are 10.01 and (D) same as molecular weight
11.01. The atomic weight of natural boron is
Q.9 The difference in the oxidation numbers of
10.81. Calculate the percentage of each isotope
the two types of sulphur atoms in Na 2S4O6 is.
in natural boron. (1978)

Q.2 The vapour density (hydrogen = 1) of a Assertion and Reason


mixture consisting of NO2 and N2 O 4 is 38.3 at Read the following questions and answer as per
the direction given below:
26.7ºC. Calculate the number of moles of NO2
(A) Statement I is true; Statement II is true;
in 100 g of the mixture. (1979) Statement II is the correct explanation of
Q.3 A solid mixture (5.0 g) consisting of lead Statement I.
nitrate and sodium nitrate was heated below (B) Statement I is true; Statement II is true;
600ºC until the weight of the residue was Statement II is not the correct explanation of
constant. If the loss in weight is 28.0 percent, Statement I.
find the amount of lead nitrate and sodium (C) Statement I is true; Statement II is false.
nitrate in the mixture. (1990) (D) Statement I is false; Statement II is true.

Q.4 'A' is a binary compound of a univalent Q.10 Statement I: In the titration of Na 2CO3
metal. 1.422 g of A reacts completely with 0.321 with HCl using methyl orange indicator, the
g of sulphur in an evacuated and sealed tube to volume required at the equivalent point is twice
give 1.743 g of a white crystalline solid B, that that of the acid required using phenolphthalein
forms a hydrated double salt, C with Al2 (SO4 )3 . indicator.
Identify A, B and C. (1994) Statement II: Two moles of HCl are required for
the complete neutralization of one mole of
Q.5 Calculate the molality of 1.0 L solution of Na 2CO3 . (1991)
93% H2SO4 , (weight/volume). The density of
the solution is 1.84 g/mL. (1990) Q.11 2.68  103 moles of a solution containing
n 3 
an ion A require 1.61 10 moles of MnO4
Q.6 20% surface sites have adsorbed N2 . On
n 
heating N2 gas evolved from sites and were for the oxidation of A to AO3 in acidic

collected at 0.001 atm and 298 K in a container medium. What is the value of n? (1984)
of volume is 2.46 cm3. Density of surface sites is Q.12 A 5.0 cm3 solution of H2 O 2 liberates 0.508
14 2 2
6.023 × 10 /cm and surface area is 1000 cm , g of iodine from an acidified KI solution.
find out the number of surface sites occupied Calculate the strength of H2 O 2 solution in
per molecule of N2 . (2005)
terms of volume strength at STP. (1995)
Q.7 If 0.50 mole of BaCl2 is mixed with 0.20 Q.13 A solution of 0.2 g of a compound
mole of Na3PO4 , the maximum number of containing Cu2 and C 2O24 ions on titration
moles of Ba3 (PO4 )2 that can be formed is with 0.02 M KMnO4 in presence of H2SO4
(1981) consumes 22.6 mL of the oxidant. The resultant
(A) 0.70 (B) 0.50 (C) 0.20 (D) 0.10 solution is neutralized with Na 2CO3 , acidified
Q.8 In the standardization of Na 2S2O3 using with dilute acetic acid and treated with excess
K 2Cr2O7 is (2001) KI. The liberated iodine requires 11.3 mL of 0.05
M Na 2S2O3 solution for complete reduction.
(A) (molecular weight)/2
(B) (molecular weight)/6 Find out the mole ratio of Cu2 to C 2 O 4 2 in the

1.22
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Stoichiometry and Redox Reactions

compound. Write down the balanced redox


reactions involved in the above titrations.
(1991)

Q.14 A mixture of H2C2O4 (oxalic acid) and


NaHC2O4 weighing 2.02 g was dissolved in
water and the solution made up to one litre.
Ten millilitres of the solution required 3.0 mL of
0.1 N sodium hydroxide solution for complete
neutralization. In another experiment, 10.0 mL
of the same solution, in hot dilute sulphuric
acid medium, required 4.0 mL of 0.1 N
potassium permanganate solution for
complete reaction. Calculate the amount of
H2C2O4 and NaHC2O4 in the mixture. (1990)

1.23
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Stoichiometry and Redox Reactions

PLANCESSENTIAL QUESTIONS

EXERCISE 1 JEE MAIN/BOARDS


Mole Concept
Q.1 Q.3 Q.7 Q.11 Q.13 Q.18

Q.21 Q.29
Redox

Q.3(C) Q.4 (F) Q.15 Q.19

EXERCISE 2 JEE MAIN/BOARDS


Mole Concept

Q.1 Q.6 Q.10 Q.15 Q.19 Q.23

Q.29 Q.33
Redox

Q.1 Q.8 Q.15 Q.24 Q.25 Q.35

PREVIOUS YEARS JEE MAIN


Mole Concept and Redox

Q.1 Q.5 Q.14

EXERCISE 1 JEE ADVANCED


Mole Concept
Q.3 Q.7 Q.14 Q.15 Q.22 Q.26

Q.28
Redox

Q.2 Q.5 Q.13 Q.23 Q.17

1.24
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Stoichiometry and Redox Reactions

EXERCISE 2 JEE ADVANCED


Mole Concept

Q.2 Q.7 Q.13 Q.16


Redox

Q.1 Q.6 Q.9 Q.16 Q.19

PREVIOUS YEARS JEE ADVANCED


Mole Concept and Redox

Q.3 Q.14

1.25
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Stoichiometry and Redox Reactions

ANSWER KEY

EXERCISE-1 JEE MAIN


Mole Concept
Q.1 (i) 68.125 Kg (ii) 7.63 Kg/m2 (iii) 1.72 m (b) 4.09  10 22
Q.2 7.818  10 22 atoms Q.17 55.56 moles

Q.3 4.82  10 22 atoms Q.18 7.098  107 g mol–1


Q.29 2.03 kg
Q.4 0.437
Q.20 10 mol
Q.5 6.02  1013 g / cm3
Q.21 260 ml
Q.6 0.1 M HNO3 x
Q.22 5
Q.7 14.0 tablets y
Q.8 0.1 M Q.23 24

Q.9 (C3O4 )4  C12O16 Q.24 0.394 g

Q.10 0.44 g Q.25 79.714 gm

Q.11 35.5: 1, 35.5: 1, 1: 1 Q.26 0.744

Q.12 0.7985, 0.798 Q.27 1.125, 1.99, 2.00

Q.13 M2O3 Q.28 0.302 M


Q.29 1800 mL
Q.14 K 2MnO4
Q.15 (i) 55.5 M

Q.16(a) 3.24  10 22 g/molecule

Redox Reaction
Q.1 (a) 5/2 (b) +2 (c) +3 (d) +6 (e) +2 (f) +6

(g) +2 (h) –2 (i) +5/2 (j) +1 (k) +3 (l) +8/3


(m) +7 (n) 0 (o) +5

Q.2 (a) 5Br   BrO3  6H  3Br2  3H2O

(b) 8G2O72  24H2S  164 8Cr2O3  3S 8  32H2O

(c) Au  2NO3  4Cl  4H  AuCl4  2NO2  2H2O

(d) 3Cu2O  14H  2NO3  6Cu2  2NO  7H2O

(e) 3MnO4  4H  2MnO4 1  MnO2  2H2O

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Stoichiometry and Redox Reactions

(f) 2Cu2  SO2  2H2O  2Cu  4H  SO4 3

(g) 5Cl2  I2  3H2O  2IO3  10Cl  6H

(h) 5Fe(CN)64  188   61MnO4  5Fe 3  30CO2  30NO3  61Mn 2  94H2O

(i) 6Cu3P  124H  11Cr2O72 18Cu2  6H3PO4  22Cr 3  53H2O

Q.3 (a) 2Cu2  2I  2Cu  I2

(b) 6Fe3 O4  2MnO41  H2O  9Fe 2O3  2MnO3  2OH

(c) 3C2H5 OH  2MnO4  OH  3C 2H3O  2MnO2 (s)  5H2O


(d) 2CrI3  27H2O2  10OH  2CrO4 2  6IO4  32H2O

(e) 258KOH  K 4Fe(CN)6  61Ce(NO3 ) 4 


61Ce(OH)3  Fe(OH)3  36H2O  6K 2CO3  250KNO3

Q.4 (a) H2O2  2I  2H  2H2O  I2

(b) 2Cu2  2I  2Cu  I2

(c) 3CuO  2NH3  2Cu  N2  3H2O

(d) 3H2SO3  Cr2O72  8H  3H2SO4  2Cr 3  4H2O

(e) Cr2O72  3C2H4O  8H  3C 2H4O2  2Cr 3  4H2O


(f) 2SbCl3  KIO3  6HCl  2SbCl5  ICl  3H2O  KCl

(g) As2S5  2HNO3 5H2SO4  40NO3  2H5 AsO4  12H2O

EXERCISE-2 JEE MAIN


Mole Concept
Q.1 B Q.6 B Q.11 C Q.16 C Q.21 A Q.26 C Q.31 B
Q.2 C Q.7 D Q.12 A Q.17 D Q.22 C Q.27 D Q.32 A
Q.3 B Q.8 C Q.13 B Q.18 A Q.23 B Q.28 A Q.33 C
Q.4 B Q.9 A Q.14 C Q.19 B Q.24 C Q.29 C
Q.5 B Q.10 A Q.15 A Q.20 C Q.25 B Q.30 C

1.27
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Stoichiometry and Redox Reactions

Redox Reaction
Q.1 A Q.7 B Q.13 C Q.19 A Q.25 C Q.31 C Q.37 B
Q.2 D Q.8 C Q.14 B Q.20 A Q.26 A Q.32 C
Q.3 A Q.9 B Q.15 C Q.21 C Q.27 A Q.33 C
Q.4 C Q.10 C Q.16 D Q.22 A Q.28 D Q.34 D
Q.5 C Q.11 D Q.17 C Q.23 D Q.29 C Q.35 B
Q.6 C Q.12 C Q.18 D Q.24 B Q.30 D Q.36 A

PREVIOUS YEAR'S QUESTIONS JEE MAIN


Q.1 C Q.3 D Q.5 A Q.7 C Q.9 C Q.11 C Q.13 A
Q.2 C Q.4 B Q.6 C Q.8 A Q.10 D Q.12 D Q.14 A

EXERCISE-1 JEE ADVANCED


Mole Concept
Q.1 116.8 gm Q.18 12.9 gm
Q.2 9.12 Q.19 1.14 gm
Q.3 5.6 Q.20 SO 4 2 ion concentration = 6.528
Q.4 0.597 g
Q.21 27.27%
Q.5 BaCl2 .2H2O  7.038 g,H2O  42.962 g Q.22 C2H6  0.66, C2H4  0.34
Q.6 120 g
Q.23 Pb(NO3 )2  3.32g,NaNO3  1.68 g
Q.7 20.78%
Q.24 0.0075, [Pb 2 ]  0.0536 M,
Q.8 NaOH = 0.06 g per 200 mL, Na 2CO3
=0.0265 g per 200 mL [NO3  ]  0.32 M, [Cr 3 ]  0.0714 M,
Q.9 0.1185 Q.25 %NaCl = 77.8%
Q.10 45% Q.26 (i) Fe 2O3  2Al  Al2O3  2Fe;
Q.11 61.5 gm
(ii) 80: 27; (iii) 10,000 units
Q.12 320.3 gm Q.27 12.15 gm,
Q.13 6% N2  14.28%,H2  42.86%,NH3  42.86%
Q.14 8.097 mL
Q.28 0.9413 gram
Q.15 6.125 g/litre
Q.29 (i) 0.5, 0.5; (ii) 0.66, 0.33; (iii) 1, 2
Q.16 55.53 litre
Q.30 13.4 ml
Q.17 K 2CO3  96%,Li2CO3  4%

1.28
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Stoichiometry and Redox Reactions

Q.31 AlCl3=33.33%;NaHCO3=50;KNO3=16.67 Q.33 75%


Q.32 9.4 gm Q.34 0.532: 1.00

Redox Reaction
Q.1 (a) +3 (b) 0 (c) +7 (d) +6 (e) +2 (f) +3 (g) +6 (h) 0 (i) 0 (j) –1

Q.2 Oxidized: KI,Na 2S,NH4 ; Reduced: CuSO4 , SO2 ,NO2

Q.3 (a) 8 electrons, (b) electrons


Q.4 (a) Oxidation number of sulphur in H2S and SO2 are respectively –2 and +4.

Q.5 NO2 is oxidized to NO3 by MnO4 (in basic medium) which is reduced to MnO2 .
MnO 4  NO 2  NO 3  MnO 2
7 3 5 4

oxidation

reduction

Thus, MnO4  MnO3 oxidation number decreases by 3-units

NO2 NO3 oxidation number increases by 2 units

Thus, 2MnO4  3NO2


3
MnO4  NO2  1.5 mol NO2
2
Q.6 (a) HSO3 (b) NO2 (c) Cl

Q.7 (a) 4Zn  10HNO3  4Zn(NO3 ) 2  N2O  5H2O

(b) 6HI  2HNO3  3I2  2NO  4H2O


Q.8 25 litre Q.9 0.5 N, 0.167 M
Q.10 0.085 M, 0.042 N Q.11 54%
Q.12 (i) 85%; (ii) 124.79 mL Q.13 30.33%
Q.14 (i) 3 2 8 3 1 2 11

(ii) 1 40 40 12 2 5
(iii) 2 27 64 6 2 54 32
(iv) 3 14 18 14 6 9

Q.15 (i) As2S3  12OH  14H2O  2As3O4  3S2O4  20H2O

(ii) 2CrI3  10OH  27H2O2  2Cr 2O4  6IO4  32H2O



(iii) P4  3OH  3H2O  3H2PO2  PH3

1.29
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Stoichiometry and Redox Reactions

(iv) 3As 2S3  4H2O  10NO3  10   6H3 AsO4  9S  10NO


Q.16 0.1716 Q.17 +3

Q.18 FeC2O4  0.03N,FeSO4  0.03N Q.19 Molar ratio = 1: 1

Q.20 40 mL Q.21 14%

Q.22 57.4% Q.23 1.847  10 3%


Q.24 [Fe3 ]  0.1M,[MnO4 ]  0.105M Q.25 (i) 0.08 N, 0.136%, 0.448 volume; (ii) 1.344

Q.26 0.062 M Q.27 1.338 g

Q.28 (a) 6H  ClO3  5Fe 2  Cl  5Fe 3  3H2O

(b) 24CuS  16NO3  64H  24Cu2  3S8  16NO  32H2 O

(c) S2O32  Sb 2O5  4H  2SbO  2H2SO3

(d) 16HCl  2KMnO4  5Cl2  2KCl  2MnCl2  8H2O

(e) 3KClO3  3H2SO4  3KHSO4  HClO4  2ClO2  H2O

(f) 2HNO3  6HBr  2NO  3Br2  4H2O (g) IO4  7I  8H  4I2  4H2O

Q.29 (a) Cu  4H  2NO3  Cu2  2NO2  2H2O

(b) Cl2  IO3  2OH IO4  2Cl  2H2O

(c) 3H2S  2K 2CrO4  5H2SO4  Cr2 (SO4 )3  2K 2SO4  8H2O  3S

(d) 5Fe 2  MnO4  8H  5Fe 3  Mn2  4H2O

(e) 2KMnO4  3H2SO4  5H2O2 K 2SO4  2MnSO4  8H2O  5O2

(f) 2H2O2  2MnO2  2OH  2MnO4  4H2O

Q.30 (a) S2O42  Ag2O  2OH  2Ag  2SO32  H2O

(b) Cl2  2OH  Cl  ClO  H2O

(c) 3H2  2ReO4   2ReO2  2H2O  2OH

(d) 2ClO2  SbO2  2OH  2H2O  2ClO2  Sb(OH)61

(e) 6I2  12OH 10I  2IO2  6H2O

(f) MnO4  5Fe 2  4H2O Mn2  5Fe 3  8OH

1.30
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Stoichiometry and Redox Reactions

EXERCISE-2 JEE ADVANCED


Mole Concept
Q.1 D Q.7 A Q.13 (A) C; (B) A; (C) A
Q.2 B Q.8 C Q.14 A-R, B-P, C-Q
Q.3 C Q.9 A Q.15 A-R, B-Q, C-P
Q.4 B Q.10 A Q.16 C
Q.5 A Q.11 C Q.17 B
Q.6 A; C; D Q.12 (A) C; (B) A; (C) B; (D)A

Redox Reaction
Q.1 C Q.4 D Q.7 A Q.10 D Q.13 C Q.16 A,B,D
Q.2 D Q.5 C Q.8 B Q.11 D Q.14 B,C Q.17 A
Q.3 C Q.6 A Q.9 D Q.12 D Q.15 B Q.18 D
Q.19 1  h, 2  i, 3  f, 4  a, 5  g, 6  b, 7  c, 8  d, 9  e

Q.20 a  (P,S); b  (R); c  (P,Q); d  (P)

PREVIOUS YEAR'S QUESTIONS JEE ADVANCED


Q.1 20% Q.7 D Q.13 Moles of Cu2 ;
Q.2 0.437 Q.8 B Moles of C 2 O 4 2 = 1:2
Q.3 1.7 g Q.9 5
Q.14 0.9 g, 1.12 g
Q.4 A = KO2 Q.10 B
Q.5 10.43 Q.11 2
Q.6 2 Q.12 4.48 V

1.31
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Stoichiometry and Redox Reactions

SOLUTIONS
EXERCISE – I JEE MAIN

Mole Concept =
3  19  1.67  1027  103 gm
4    (5  103 )3  (1010 )3 cm3
Sol.1 (i) 125 pound
1 pound = lb = 545 gm 95.19  1027  1030
= gm/cm3
125 pound = 125 × 545 gm 1570.79  109
= 125 × 545 × 10–3 kg = 68. 125 kg = 6. 02 × 1013 gm/cm3
(ii) 14 lb/m2
1lb = 545 gm Sol.6 mole = M1V1
In SI units = 14 × 545 × 10–3 kg/m2 for neutralisation HHNO  HNaOH
3
= 7. 63 kg/m2
M1V1 = M2V2
(iii) 5’8’’
20 × M1 = 0. 08M × 25
(1’ = 12’’)
0.08  25
5’8’’ = (12’’ × 5) + 8’’ = 68’’ M1   0.1M
20
= 68 × 2. 54 cm = 1. 72 m
Sol.7 HCl produced perday
Sol.2 Mavg. = (0. 932) 39 + (0. 068)41 = 39. 136
= 3. 0 gm × 2. 5 = 7. 5 gm
Mass of 2g-atoms = 2 ×39. 136 gm
7.5
Mass of ‘’41K’’ in 2g-atoms = mole
36.5
= 2 × 39. 136 × (0. 068)
moles of Al(OH)3 in an antacid tablet
number of atoms 3 0.4
2  39.136 = 400  10 = mole
=  (0.068)  6.023  1023 (27  51) 78
41
= 7. 818 × 1022 3 × mole of Al(OH)3 = moles of HCl
0.4 7.5
3×n× =
Sol.3 Barium phosphate = Ba3(PO4)2 78 36.5
no. of oxygen atoms n  14
6.025 Sol.8 HCl + AgNO3 AgCl + HNO3
=  8  6.023  1023 = 4. 82 × 1022 atoms
602.5 0.1435
M × 10 × 10–3 =
Sol.4 Molecular weight = Vapour density × 2 108  35.5
= 76. 6 M = 0. 1 M.
Let’s suppose x % mole of NO2 is there Sol.9 Lets it is CxOy
76. 6 = x (46) + (1 – x) 92 x(12) + y(16) = 400
46x = 15. 4 x(12)
x = 33. 47% = mole fraction of NO2  0.36
400
100
Total mole = = 1. 305 mole x = 12;y = 16
76.6 the formula is C12O16 = (C3O4)4
mole of NO2 = (0. 3347) × (1. 305)
= 0. 437 mole. Sol.10 CxHy + O2 H2O + CO2
0. 1 mole 0. 2 mole
Sol.5 Correction : radius of fluorine 0.18
= 5 × 10–3 A0 Mole of H2O =  0.1 mole
18
mass of nucleous = 19 × 1. 67 × 10–27 kg
mole of CO2 = 0. 02 mole
volume of nucleous 1
4 mole of O2 required = (0.1)  0.02
= × × (5 × 10–3)3 cm3 2
3
= 0. 07 mole
density

S 1.1
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Stoichiometry and Redox Reactions

y = mole of H = (0. 1)2 = 0. 2 mole Sol.16 (a) mass = (8 × 12) + (10 × 1)


x = mole of C = 0. 02 mole +(4 × 14) + (2 × 16)
mass of hydro is = (0. 02)12 + (0. 2)1 = 96 + 10 + 56 + 32
= 0. 24 + 0. 2 = 0. 44 gm. Mass = 194 amu
= 194 × 1. 66 × 10–24 gm/molecule
Sol.11 PCl3 & PH3
= 3. 24 × 10–22 gm/molecule
2257% 91. 18%
(b) molecular mass of Cl2 = 71
mass of Cl in PCl3 = 3 × 35. 5 = 106. 5
Total no. of electrons in one molecule of
mass of H in PH3 = 3 × 1 = 3
Cl2 = 34
106.5 
ratio   35.5  equal . So no. of electrons
3 : H  35.5
Ratio of Cl 0.142

 = × 34 × 6. 023 × 1023 = 4. 029 × 1022
Hence prove. 71

Sol.12 Exp. (I) CuO Cu + X Sol.17 Molarity = moles per. litre moles per
Ratio of mass of litre
1.098 Mass density  Volume
Cu : CuO =  0.7985 =  =
1.375 18  V 18  Volume
HNO
3  Cu(NO )  1000
Exp. (II) Cu  3 2  CuO  55.55M
1.179 gm 1.476 18
Ratio of mass of
Sol.18 Volume of plant virus = (r2h)
1.179
Cu : CuO =  0.798 = × (75 × 10–10)2 × (5000 × 10–10)
1.479
= 8. 835 × 10–23 m3
both ratio are same. Hence prove.
= 8. 835 × 10–23 × (10+2)3 cm3
Sol.13 MxOy = 8. 835 × 10–17 cm3
17
x × atomic mass of M = 0. 540 …. (i) Mass = 8.835  10 gm
y × 16 = 1. 020 – 0. 540 0.75
y = 0. 03 = 11. 78 × 10–17 gm
Dulong-Pelit law (atomic mass of M) = 11. 78 × 6. 023 × 10+23 × 10–17
× 0. 216 = 5. 83 = 7. 098 × 107 g mol–1
atomic mass of M ~ 27 . . . . (ii)
Sol.19 25% of heavy water = 0. 5 litre.
Petit x × (27) = 0. 540
mass of heavy water
x = 0. 02
= 0. 5 × 103 × 1. 06 gm/cm3 = 530 gm
formula of metal oxide = M2O3.
mass of normal water
Sol.14 Let’s say substance is 100 gm = 1. 5 × 103 × 1 gm/cm3 = 1500 gm
39.7 Total mass = 2030 gm = 2. 030 kg
moles of K =  1.017
39
Sol.20 SO2Cl2 + 2H2O H2SO4 + 2HCl
29.9
moles of Mn =  0.5436 Initially 2. 5 0 0
55
after 0 2. 5 5
100  39.7  29.9
moles of O =  1.9 for 2. 5 moles of H2SO4, KOH = 5 mole
16
for 5 mole of HCl, KOH = 5 mole
so by seeing on ratio of K : Mn : O
total KOH = 5 + 5 = 10 mole
empirical formula is K2MnO4.
Sol.21 NH4Cl + MgCl2 + AgNO3 
no. of moles
Sol.15 Molarity =
volume (in litre) 2 % by mass 5% by mass
mass 1000  0.997 AgCl + NH4NO3 + Mg(NO3)2
No. of moles =  per litre.
18 18 d = 1040 gm/lit.
molarity = 55. 38 M moles of Cl– in

S 1.2
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Stoichiometry and Redox Reactions

2 1
NH4Cl = = 0. 0373 mole
(14  4  35.5) Total mole of KClO3 =
39  35.5  48
moles of Cl– in = 8.163 × 10–3 mole
2
MgCl2 = 2 × = 0. 0421 mole moles of KClO3 in IInd reaction
(24  71)
= 3.794 × 10 moles
Total mole of Cl– moles of KClO4 produced in IInd
= Total mole of AgNO3 required reaction = 2.8496 × 10–3 mole
= 0. 0421 + 0. 0373 = 0. 07940 mole mass of KClO4 = 2.8456 × 10–3 ×
Mass of AgNO3 = 0. 07940 × 170
(39 + 35.5 + 64) = 0.394 gm
= 13. 49 gm
mass of solution of Sol.25 Let’s say we have 100 gm mix.
100 Fe3O4 = FeO. Fe2O3 FeO + Fe2O3
AgNO3 × 13. 49 ×  269.97gm
5 x gram 0. 310 gram 0. 680x gram
269.97 initially FeO (100 – x) gram
Volume required = cm3 = 259. 59
1.04 total (FeO) (100 – x + 0. 310 x) gm
cm3 = (100 – 0. 690 x) gm
1
Sol.22 Oxalic acid = H2C2O4 2FeO  O2  Fe2O3
2
formic acid = HCOOH
(105 – 0. 690x)gm
2 2
H2C2O4 + H2SO4  SO 4  H4 C2O 4  100  0.690x  (105  0.690x)
2 
HCOOH + H2SO4  2
 SO 4 + +
2H  72  160
+HCOOH 160
(100 × 0. 690x) ×  105  0.690x
36
H4 C2O24  KOH  C2O24
4000 – 27. 6 x = 945 – 6. 21 x
Sol.23 CH4 x mole molecular weight = 16 3055 = 21. 39 x
(C2H4) y mole molecular weight = 28 x = oxygen external = 5gm
Mean molecular weight 5
= mole
32
= 20  x(16)  y(28)
xy So moles of FeO that was present
(100  0.690x) 4  5
20 = 16 + 12y 
xy 56  16 32
y Fe3O4 + x = 79. 71 gm
0. 33 =
xy FeO = 100 – x = 20. 29 gm
x
 0.66
xy Sol.26 Zn + 2I ZnI2
x:y=2:1 m m
If x : y = 1 : 2 2x moles of Zn = moles of I
then mean molecular weight (to complete reaction)
1(16)  2(28) m
= =24 2× = 2x moles of Zn
3 65
Sol.24 m
= moles of I
127
2KClO3 2KCl + 3O2 Since moles of I < 2x moles of Zn
4.369 × 10–3 6.55 × 10–3 So Zn will be left unreacted
4KClO3 3KClO4 + KCl m m
Zn unreacted =  mole
3.794 × 10–3 2.845 × 10–3 65 127  2
moles of oxygen produced 65
mass Zn unreacted = m  m
146.8  103 254
= = 6.55 × 10–3 mole
22.4 = 0. 744 m

S 1.3
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Stoichiometry and Redox Reactions

Sol.27 mole of P4 =
2

1
mole Redox Reactions
4  31 62 Sol.1 (a) (N2H5)2 SO4
2 1
moles of O2 =  mole
2  16 16 2
P4 + 3O2 P4O6 +
2(N2H5) + SO24
x 3x 0 initial
0 0 x after
2Nx– + 5H+
P4 + 5O2 P4O10
y 5y 0 initial 5
oxidation number of N = –
0 0 y after 2
1  5
xy   0.0161  –2x + 5 = 0;x =
2
62 1  by solving
3x  5y   0.0625 (b) Mg3N2  3Mgx+ + 2N3–
16  3x – 6 = 0
–3
y = 7. 056 × 10 x=2 Mg2+
x = 9. 0435 × 10–3 (c) [Co(NH3)5Cl]Cl2
mass of P4O6 = 9. 0435 × 10–3
[(4 × 31) + (6 × 16)] [Co(NH3)5Cl]+2 2Cl–
= 1. 9895 gm
Co2+ + (NH3)5 Cl–
mass of P4O10 = 7. 056 × 10–3
x – 1 = +2 x = +3
[(4 × 31) + (10 × 16)]
Co+3
= 2.003 gm
(d) K2FeO4
2.7 2K+ Fex + 4O2–
Sol.28 moles of aluminium =  0.1 mole
27 +2 + x – 8 = 0;x = +6
moles of H2SO4 in solution Fe+6
(1.18  100)  0.25 (e) Ba(H2PO2)2
= = 0. 3010 mole
98 Ba2+ (H2PO2)–
2Al + 3H2SO4 Al2(SO4)3 + 3H2 2H+ + Px+ + 2O2–
For consumption of Al, required mole of 2 + x – 4 = 0;x= +2
3 P+2
H2SO4 = (0. 10) × = 0. 15 mole
2 (f) H2SO4
remaining mole of + 2 + x – 8 = 0;x = +6
H2SO4 = 0. 3010 – 0. 15 = 0. 151 mole S+6
0.151 (g) CS2
molarity =  1000  0.302M
500 – 4 + 2x = 0;x = +2
Sol.29 KMnO4 + H2SO4 K2SO4 + MnSO4 S+2
+ H2O + (O) …. (1) (h) S–2
FeC2O4 + H2SO4 FeSO4 + H2C2O4 (i) Na2S4O6
…. . (2) +2 + 4x – 12 = 0
FeSI4 + H2C2O4 + H2SO4 + O  S+5/2
Fe2(SO4)3 + CO2 + H2 …. . (3) 5
x=+
3KMnO4 + 5FeC2O4 Fe3+ + 2CO2 + Mn2+ 2
(1.5) (j) S2Cl2
(0. 5)V = 3
5 +2x – 2 = 0;x = +1
V = 1. 8 lit. = 1800 mL S+1
(k) RNO2
+1 + x – 4 = 0;x = 3
N+3
(l) Pb3O4

S 1.4
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Stoichiometry and Redox Reactions

+3x – 8 = 0 AuCl4 + 2NO2 + 2H2O


8
x=+ Pb+8/3 (d) Cu2O + 2H+ 2Cu+2 + 2e– + H2O
3
…. (1)
(m) S2O28 
H+ + NO3 + 3e– NO + 2H2O
2x – 16 = –2
. …(2)
2x = 14;x = +7
(3 × (1)) + (2 × (2))
S+7

(n) C6H12O6 3Cu2O + 6H+ + 8H+ + 2NO3 
6Cu2+ + 3H2O + 2NO + 4H2O
+6x + 12 – 12 = 0;x = 0

C° 3Cu2O + 2NO3 + 14H+ 
(o) Mg2P2O7s 6Cu2++ 2NO + 7H2O
+2(2) + 2x – 14 = 0 6 7 2

x = +5 (e) MnO24  MnO4  MnO2


P+5 6

(p) KClO3 4H  MnO24  2e MnO2 + 2H2O


+1 + x – 6 = 0;x = +5 …. (1)
Cl+5
MnO24 MnO4  e …. . (2) × 2
1 5 0 3MnO24  4H 
Sol.2 (a) Br  BrO3  H Br2 + H2O

MnO2 + 2MnO 4  2H2O
1
Br–1  Br2 + e– ……(1) 2
2 (f) Cu2+ + SO2 Cu+ + SO4
 1 Cu2+ + e– Cu+× (2)
5e– + BrO3 + 6H+  Br2 + 3H2O
2 2
H2O + SO2 SO4 + 2e– + 4H+
……(2)
((1) × 5) + (2) 2Cu2+ + SO2 + 2H2O 
2
5Br   BrO3  6H 3Br2 + 3H2O 2Cu+ + SO4 + 4H+
2 o o o
2
(b) H2S  Cr2O27 
 H  (g) Cl2  I2  IO3  Cl
3 0 2e– + Cl2 2Cl–× (5)
Cr2O3  S8  H2O 
3H2O + I2  2IO3 + 10e– + 6H+
1
H2S  S8  2e  2H ……(1) 3H2O + 5Cl2 + I2  2IO 3 +10Cl–+6H+

8
2  (h) Fe+2 Fe+3 + e–
8H+ + Cr2O7  6e Cr2O3 + 4H2O
4
2H2O + 6C+2  6CO 2 + 6(2e–) + 24H+
……(2)
5
((1) × 3) + (2)
8H2O + 6N  6NO 3 + 6(8e–) + 36H+
3–
3H2S + Cr2O72 +
+ 2H 
7
3 5e + MnO 4 + 8H+ Mn2+ + 4H2O × (6H+)

 S8 + 6H+ + Cr2O3 + 4H2O
8
Fe(CN)64  + 30H2O Fe3+ + 6CO2
8Cr2O72 + 24H2S + 16H+ 
8Cr2O3 + S8 + 32H2O
6NO3 + 60H+ + 61e– × (5)
 
(c) Au + 4Cl–  AuCl4 + 3e– …. . (1)
5Fe(CN)64   61MnO4  188H 5Fe+3
NO3 – +
+ e + 2H NO2 + H2O . …(2)

+30CO2 + 30NO3 + 61Mn2++94H2O
(1) + (2 × (2))
 (i) Cu+1  Cu+2 + e– × (3)
Au + 4Cl– + 2NO3 + 4H+ 

S 1.5
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Stoichiometry and Redox Reactions

5 1 1
P3  4H2O H3PO 4 + 8e– + 5H+ H2O2 21e
  H2O
–2

Cu3P + 4H2O 3Cu2+ + H3PO4 + 


5H+ + 11e– 2I+ H2O2 H2O + I2 + 2H+ OH
6 2HI + H2O2 2H2O + I2 + H
Cr2O72  3e + 14H+ Cr+3 + 7H2O (b) Cu+2 + ICu+ + I2
1e
6Cu3P + 124H+ + 11Cr2O72 18Cu2+ (Cu+2 
 Cu+) × 2
+ 6H3PO4 + 22Cr+3 + 53H2O 1e
(I   I) × 2

2Cu+2 + 2I2Cu+ + I2
By the oxidation number method,
Sol.3 (a) 2Cu2+ + 2I- 2Cu + I2
(1)
8/3 3
(b) Fe3O 4 + 4H2O Fe2O3 + 0
– – Cu+2 +2ICu+ I2
8OH + 2e × (3)
7
3OH– + MnO 4 + 3e–  (2)
MnO2 + 2H2O × (2) To balance the electrons transferred,
3Fe3O4 + 12H2O + 8OH + – 2MnO4  2Cu+2 + 2I2Cu+ I2
To balance charges on both sides,
3Fe2O3 + 24OH– + 4H2O

2Cu+2 + 2I+ 2H2Cu+ I2 + H2O
6Fe3O4 + 2MnO 4 + 8H2O 2Cu+2 + 2HI 2Cu+ I2 + H2O
9Fe2O3 + 16OH–+2MnO3
2 (c) CuO + NH3 Cu + N2 + H2O
(c) C2H5OH + OH–  2e
1 0 0
+2
 C2H3O + H2O Re– CuO + NH3Cu + N2 + H2O
–3
7 4
3e–+ MnO4 + 4H2O MnO 2 + 8OH–
3e–

 To balance the electrons transferred
3C2H5OH + 2MnO 4 + OH– 
3CuO + 2NH3 2Cu + N2 + H2O
3C3H3O– + 2MnO2 + 5H2O
6 to balance oxygen
+3
(d) Cr + 8OH –
 CrO24 + 4H2O + 3e –

+2 –1 0 0
7
3I– + 8OH–  3IO 4 + 24e– + 4H2O H2SO3 + Cr2O H2SO4 + 2Cr+3
2
7
(d) (+4) (+12) (+6) (+6)

e + H2O21  H2O H2O + 2OH 2 –

 (2e–) (6e)


2CrI3 + 27H2O2 + 10OH–  To balance the number of electrons
2CrO24 + 6IO4 + 32H2O transferred,
2
9H2SO3 + Cr2O7 9H2SO4 + 2Cr+3
(e)258KOH+K4Fe(CN)6+61Ce(NO3)4
61Ce(OH)3+ Fe(OH)3+ 36H2O + 6K2CO3+ 250KNO3 To balance charges on both sides,
2
3H2SO3 + Cr2O7 + 8H 3H2SO4 +
Sol.4 (a) + H2O2 H2O + I2
I
(acidic medium) 2Cr+3 + 4H2O
1
 1e  0 We observe that
(I   I2 )  2
the number of oxygen atoms are
simultaneously balanced

S 1.6
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Stoichiometry and Redox Reactions

(e) (i) Add H2O to the side which is oxygen


(–2)
deficient
Cr2O27 + C2H4O C2H4O2 + 2Cr+3 (ii) Add H+ to the side which is hydrogen
(+12) (+3)
(2e) deficient
2. Basic Medium :-
(9e) (i) Add OH– to the side which has less -ve
(as this is an
Oxidation charge
reaction) (ii) Add H2O to the side which is oxygen
deficient
2 (iii) Add H+ to the side which is hydrogen
 Cr2 O7 + C2H4O 9C2H4O2 + 4Cr+3
deficient
To balanced charges on both sides, 3. Oxidation State Method :-
2
 2Cr2O7 + 9C2H4O + 16H This method is based on the fact that the
9C2H4O2 + 4Cr+3 + 8H2O number of electrons gained during reduction
3 5 must be equal to the number of e–s lost during
(f) 3Cl– + SbCl3  SbCl5 + 2e– × (2) oxidation.
5 1 Sol.7 Definition of redox reaction :-
6e– + KIO3  6H  I + 3H2O + K+
Reaction which involves change in oxidation
 state of their atom, generally involve the
2SbCl3 + KIO3 + 8HCl 2SbCl5 + transfer of electron between species.
ICl + 4H2O + KCl So, the most essential conditions that must be
satisfied is the exchange of electron change in
5
oxidation state.
(g) As2S52
5 Sol.8 No, oxidation state term is just
As  H3 AsO4 No redox charge
+5
introduced to easily calculate the exchange of
6 electron in redox reaction.
5S2– + 4H2O 5H2SO 4 + 40e- So, oxidation no. of an element in a particular
5 4 compound represents the no. of e–s lost or
e– + HNO3  H NO2 + H2O gained by an element during its change from
 free state into that compound or it represent
As2S5 + 2HNO3 5H2SO4 + the extent of oxidation or reduction of an
40NO2 + 2H3ASO4 + 12H2O element during its charge from free state into
that compound.
Sol.5 Disproportionation is a specific type of
redox reaction in which a species is Sol.9 Redox Couple :-
simultaneously reduced and oxidized to form Oxidation half reaction and reduction half
two different product. reaction contributes to redox couple
2  M M+n + ne– Oxidation
Eg. MnO 4 MnO 4 + MnO2
6 7 4
A + ne– A–n Reduction

Sol.6 Ion-electron method :- M + A M+n + A–n
(I) Divide the complete equations into two half
Sol.11 (a)
reaction.
(II) Balance the atoms in each half reaction MnO4 + C2H2O 4  2
Mn(aq.
) +
(aq.) (aq.)
separately according to the following steps :-
(a) Balance all atoms other then O and H CO2(g)  H2O( )
(b) for O and H
1. Acidic Medium :-

S 1.7
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Stoichiometry and Redox Reactions

(c) Displacement reaction :-


Reaction in which on element or ion moves
out of ore compound and into another
Oxidant Reductant Reductant Oxidant Eg. Fe + CuSO4 Cu + FeSO4
(i) Ion-electron method :-
7 Sol.16 Oxidation No. :-
MnO 4 Mn+7 5e– ) × 2 No. of e–s lost or gained by an element during
3 2 8  4 its change from free state into compound or
2e
C2 H2 O4   CO2 2e– ) × 5 represent the extent of oxidation / reduction
 of an element during its change from free
state into that compound.
2MnO4  5C2H2O4 2Mn 2 +10CO2
Valence :- Number of valence bonds a given
(ii) Oxidation number method :- atom has formed or can form with one or
MnO4  C2H2O4 Mn+2 + 2CO2 more than one with other atoms.
(+7) (+6) (+2) (+4)

Sol.18 Half Reaction :-


5e– 2e –
This is either the oxidation or reduction
2 0 reaction component of a redox reaction. This
(b) H2S(aq.) + Cl2(aq)  S (S ) + Cl(aq.)

is obtained by considering the change in
oxidation states of individual substances
involved in the redox reaction
Zn + CuSO4 ZnSO4 + Cu
Zn  Zn2+ + 2e–
Reductant Oxidant
oxidation half reaction
H2S–2 S + 2e– + 2H+
2
Cl2 + 2e– 2Cl– e– + CuSO4 Cu + SO4
 Reduction half reaction.
0 0
H2S + Cl2  S + 2Cl–
0 0
H2S–2 + Cl2 S + 2Cl–2

–2e– +2e–
So, no need to multiply this equation with any
co-efficients.

Sol.13 Oxidation :- Increase in oxidation


number
2Cl– Cl2
Reduction :- Decrease in oxidation number
KMnO4 Mn2+

Sol.14 (a) Combination reaction :-


Reaction in which two or more elements on
compounds combine together to form a
single compound
2Mg + O2 2MgO + heat
(b) Decomposition reaction :-
Reaction is the separation of a chemical
compound into elements or simpler
compounds
2H2O2 2H2O + O2

S 1.8
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Stoichiometry and Redox Reactions

EXERCISE – II JEE MAIN


Mole Concept Sol.5 12C(s) + 11H2(g) +
11
O2(g) 
2
Sol.1 A + O2  C12H22O11(s)
M1V1 = N2V2 84 12 56
equivalent of A = equivalent of O2 12 1 22.4
x  16  7 12 2. 5
  2 Here O2 is limiting reagent
equivalent weight of A  16 
moles of C12H22O11 formed
x 2.5 5
 equivalent weight of A =  2 = mole
2 11 11
Sol.2 mass O2 in 88 gm 5
mass =  [(12  12)  22  (11  16)]
88  32 11
CO2 =  64gm = 155. 45 gm
44
64 Sol.6 M(CO3) CO2 + MO
mole of O =  4 mole
16 or
so mass of CO is = 4 × (12 + 16) = 112 gm M2(CO3) CO2 + M2O
1 mass of CO3 = 12 + 48 = 60
Sol.3 Mg + O2 MgO 12.315 12.315
2 mole of CO2 = (RT) = ×0.
(PV) 1  (12.315)
0.25 mole 0821 × 300 = 0. 5 mole
mole of M(CO3) or M2CO3 = 0. 5 mole
so mass of CO3 in carbonate
0.5 mole
= 0. 5 × 60 = 30 gram
mass of MgO = 0. 5 × (24 + 16) = 20 gm Checking all options one by one
(B) is correct.
Sol.4 let’s diabasic acid is CxHyOz
x(12) Sol.7 Empirical formula would be NH2 because
weight of C =
M ratio of N & H is given 1 : 2. By stability we see
y N2H4 is correct answer.
weight = H =
M
Sol.8 CxHy + O2 CO2 + H2O
z(16)
weight of O =
M 5V 10V 5V
x(12) = 8 × y 3x = 2y
1 10V
x(12) = × 16(z) 3x = 2z
2 by oxygen atom balance H2O = 10V
3 by hydrogen atom balance y(5) = 2(10)
y=z= x
2 y=4
empirical formula C2H3O3 by carbon balance = x(5) = 5
Ag2(CxHyOz)  
 2Ag the molecule is CH4
0.5934
108 Sol.9 Molecular weight of NO2 = 32 + 14 = 46
0.5934 1 Molecular weight of NO = 16 + 14 = 30
mole of salt =  let's x = NO 1 – x = NO2
2  108 [216  (24  3  48)x]
34 = x(30) + (1 – x) 46
216 + 75x = 364
16x = 12
x~z
3
so the formula would be = C4H6O6 x= so NO2 % = 25%
4

S 1.9
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Stoichiometry and Redox Reactions

Sol.10 5A2 + 2B4 2AB2 + 4A2B 500


A
4 mole 93
molecular mass of AB2 = 250 by conservation of silica
molecular mass of A2B = 140 500
100 
B4 = 480 93  x
A2 = 20 2
moles of AB2 to be produced x = 47. 31
1000
= = 4 mole
250 Sol.14 C2H4O2 + 2O2 2CO2 + 2H2O
moles of A2B to be produced x gm 620–x gm
1000 11 11
= = 7. 14 mole
140 x 620  x
mole
So mass of A2, B4 would to according to AB2 60 32
5 to produce maximum energy C2H4O2 & O2 will
So mass of A2 required =  4  20 = 10 × 20
2 be fully consumed.
= 200 gm x 620  x 1
x  
mass of B4 required = 4 × 480 60 32 2
= 2 × 960 gm = 1920 gm 64x = 37200 – 60x
total mass = 1920 + 200 = 2120 gm x = 300 gm
300  44
weight of CO2 = 2 ×
Sol.11 CxHyOz + O2  CO2 + H2O  60
132 gm 54 gm = 440 gm
 
3 mole 3 mole Sol.16 (organic compound) + H2O N2
0. 42 gm
y = 6 mole
10 3
x = 3 mole moles of N2 = PV  860  100 
RT 760 11 0.08  250
so option (C) is correct
86
=  5.143  104
167200
1
Sol.12 Zn + O ZnO mass of N2 = 5. 143 × 10–4 × 28
2 2
= 0. 0144 gm
x gm
0.0144 10
1 x v fraction =  0.034  %
  0.42 3
2 65 22.4
moles of H+ = (0. 1) (0. 3) + (0. 2) (0. 3) × 2
x 2x
v  11.2   5.6 lit. = 0. 15 mole
65 65
0.015
Normality =  1000  0.3N
500
Sol.13 let’s say 100 gm of clay is given initially
12 gm water
Sol.17 moles of NaOH = (0. 300) (0. 5)
x gm silica
= 0. 15 moles
y gm other
0.15
after that (100 – A)gm of clay for molarity = 0. 2 M =
V
 100  A 
(12 – A) gm water   silica V = 750 ml
 2  Volume to be added = 750 – 300
(100  A)  7 = 450 ml
(12 – A) =
100
250
1200 – 100A = 700 – 7A Sol.18 moles of water=  13.888 mole
18
93A = 500

S 1.10
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Stoichiometry and Redox Reactions

urea = NH2–C–NH2 0. 07 = [104. 94 + 17. 82 x] × 10–3


|| 35. 06 = 17. 82 x
O x~2
3
moles urea = = 0. 05 mole
60 Sol.24 Washing soda (Na2CO3) in 25 cc
mole fraction = 0.0036 = 0. 12 gm
0.12
Sol.19 P4S3 + 8O2 P4O10 + 3SO2 2  1.7  103
106  18x
384 240 = 180. 2 + 30. 6 x
moles of O2 =  12mole
32 x~2
440 percentage of carbonate
moles of P4S3 =  2 mole
124  96 106
L. R. = O2 = ~ 76%
106  36
So mass of P4O10 produced
12 Sol.25 No. of carbon atoms
=  [124  160] = 426 gm
8 3

Sol.20 PCl5 PCl3 + Cl2 = 1.2  10  6.023  1023


12
Initially1 mole = 6. 02 × 1019
1 1 1
after mole mole mole
2 2 2 Sol.26 Sol.24 31 = (0. 79) (24) + (0. 21 – x) (25)
Initially Mavg. = MPCl = 31 + 5(35. 5) = 208. + (x) (26)
5
5 24. 31 = 18. 96 + 5. 25 + x
M 208.5 x = 0. 1 = 10%
after Mavg. =  2
3/2 3
2 Sol.27 Using HPh
 208.5   
3 Na2CO3 
HCl
 NaHCO3  H
So change in Mavg. = 33. 33% NaOH  HCl
 NaCl + H
+

Using
Sol.21 3Mg + 2NH3 Mg3N2 + 3H2 MeOH
2 mole 2 mole Na2CO3  HCl
 H2CO3 + NaCl
L. R. = Mg NaOH  HCl
 NaCl + H
+

Mass of Mg3N2 produced moles of HCl used in HPh = 4m mole


2 200 moles of HCl used in MeOH = 4. 5 m mole
=  (72  28) = gm
3 3
It means that for NaHCO3 H2CO3 required
Sol.22 let’s say solution is in 100 gm. mole of HCl 0. 5 m mole
HCl mole = 1 mole moles of Na2CO3 = 0. 5 m mole
1 = 0. 5 × 10–3 × 106 gm/250 ml
molality = ×1000 = 15. 75 = 5. 3 mg/25 ml
(100  36.5)
= 2. 12 g/L
moles of solute
molality = NaOH moles = 3. 5 m mole
mass of solvent (in kg) mass of NaOH = 40 × 3. 5
= 140 mg/25 ml
Sol.23 Weight of Na2CO3.xH2O in 10 ml = 5. 6 g/L
0.025 None of these
solution =  0.07
5
0.07 9.9 Sol.28 moles of HCl = 0. 25 × 30 m mole
2   10 –3
46  12  48  x(18) 10 = 7. 5 m mole
0.14 7.5 x(0.5) (1  x)0.5
 0.99  103  103  
106  18x 2 138 74

S 1.11
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Stoichiometry and Redox Reactions

7. 5 × 10–3 Sol.1 Equivalent weight = Molecular weight ×


Solving this x ~ 96% nfactor
K2CO3 ~ 96 = (M0 )FeSO  1
4
Li2CO3 ~ 4 +2 +3
Fe Fe
Sol.29 KMnO4 + 5FeSO4 Mn2+ + Fe3+
2.0 2+
Sol.3 H2S + KMnO4 S + Mn
152
moles of KMnO4 –2e–
+5e–
2.0
= = 2. 631 × 10–3 m 1.58
5  152 2   5 =0.85
Volume × molarity = moles 34 158
3
Volume = 2.631  10 = 52. 63 ml 5 0 5 4
0.05
Sol.4 HNO3  I2  I2O5  NO2
m 127
Sol.30 Statement-I 1   10 =315
Mass of urea = 60 63 127  2
H2N–C–NH2
|| Sol.5 N1V1 = N2V2
O Oxalic acid KMnO4
10 × 10–3 × N = 20 × 10–3×0. 02 × (5)
Mass of nitrogen = 28
n-factor =0.2N
28
%=  46.66
60
m
Statement-II urea not ionic. Sol.6  2 = 10 × 10–3 × 1
34
m = 0. 17
Sol.31 Statement-I
0.17
S2O32 purity =  100  85%
0.2
2x + 3(–2) = –2
x = +2 Sol.7 KMnO4+FeC2O4 Mn2++Fe3++CO2
Statement:- Yes, Because these may be per- 3
nKMnO  5  1  (1  2) 
oxide bond. 4 5

Sol.32 Statement-I Sol.8 M2x2 + xH2 2M + xH2O


n 1 mole M2x2 gives 2 moles M
molarity = density increases n(at
v 1.05
 3.15g 
const. V) (MW) M
moles of solute 6M = 2M + x(16)
= molality =
mass of solvent 4M = x(16)
M = 4x
density increases = moles of solute 
(MW)M M
molality & molarity both changes. Now, (EW)M = 
x X
Statement-II
M
Density results in change in mass thus (EW)M = = 4.
increases moles. X
Sol.9 Oxidation means increase of oxidation
Sol.33 Statement-I no.
Incorrect because it depends in extent of losing of electrons.
reaction
Statement-II correct. Sol.10 K2Cr2O7
Redox Reactions 2K+ 2Crx+ 7O2–
+ 2 + 2x – 14 = 0

S 1.12
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Stoichiometry and Redox Reactions

x = +6 x

6 3 Sol.19 MnO 4
Sol.11 K 2Cr2O7  K 2Cr2O7 + x – 8 = –1
+6 +3 x  7
change in oxidation
No. = [3].
Sol.21 Pb2+ Pb4+ + 2e–
3 1
Sol.12 P + NaOH  PH3  NaH2PO2 Sol.22 C12 H22 O11
12x + 22 + 11(–2) = 0
P is getting oxidised and also reduced
it is oxidation and reduction x0
(D is proportionation)
2
Sol.23 SO4
Sol.13 CH2O
Cx+ 2H+ O2– Sx+ + 4O2–
x+2–2=0 x – 8 = –2
x=0 x = +6

4
Sol.14 CH4 → Cx+ + 4H+ x = –4 MnO2  4H  X 
Mn2  H2O
CH3Cl Cx+ + 3H+ + Cl– x = –2 Sol.24
CH2Cl2 x + 2 – 2 = 0 x=0 –2e–
CHCl3 x + 1 – 3 = 0 x=2 6

CCl4 x – 4 = 0 x = +4 SO32   SO24


Sol.25
Sol.15 Redox :- Exchange of electrons –2e–
change in oxidation state.
6 6 1 2
2 2
(c) Ba O2  H2SO4  Ba2 SO24  H2O2 Sol.26 S2O7
No change in oxidation +2x – 14 = –2
2x = +12; x  6
Sol.16 (a) +4 – 6 + x = 0
x = +2 S
S S
(b) + 2 + x – 8 = 0
Sol.27 S
x  6 S
S
(c) +2x – 2 = 0 S
x = +1 S8
(d) x + 5(0) = 0 8x = 0
x0 x0
1 covalency
Sol.17 (a) HClO2 + 1 + x – 2 = 0
x = +1 Sol.28 N3H
(b) HClO2 + 1 + x – 4 = 0
x = +3
1
3x + 1 = 0; x
(c) HClO3 + 1 + x – 6 = 0 3
x 5
Sol.29 K3 [Fe(CN)6]
(d) HClO4 + 1 + x – 8 = 0
+3 – (x – 6) = 0; x  3
x = +7
Sol.18 M3+ M6+ + 3e– Sol.30 MH2
+x+2=0

S 1.13
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Stoichiometry and Redox Reactions

x  2
3 5
Sol.31 PH3 to H3PO4

Sol.33 Oxidation no. of Cl = +7 it can not be


greater than this
It can get only reduced
HClO4 is an oxidising agent
 In HClO3, oxidation no. of chlorine = + 5
E. N. order O > Cl > H

2
Sol.34 Since S2 has S – S– linkage structure
2
 FeS2 Fe2+ (S – S) oxidation no. = +2

Sol.35 Yes, the given reaction is an example of


disproportionation
H2O2 is a reducing as well as an oxidising
agent
So it is not only bleaching (oxidising agent)
1 0
H2O21  H2O 2  O2
+e– 2
–e–

OH–
K2Cr2O7 K2CrO4
Sol.36
H+
orange Yellow
dichromate chromate

0 5 1

Sol.37 I2   IO3  I


 


–5e
+e–
These reactions show E° > 0
It is not feasible because iodine can show
multiple oxidation state.

S 1.14
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Stoichiometry and Redox Reactions

PREVIOUS YEARS’ QUESTIONS JEE MAIN

Mole Concept
Sol.2 (C) According to definition of molar 4H2O  3[O]
solution is one that contains one mole of a
solute in one litre of the solution. Mol. wt.
Eq. wt. 
6
Sol.3 (D) 2Al(s)  6HCl(s)  Redox Reaction
2Al3(aq)
 
 6Cl(aq)  3H2(g) Sol.7 (C) Prevent action of water and salt.

For each mole of HCl reacted, 0.5 mole of H2 Sol.8 (A)


is formed at STP. 1 6 0 4

1 mole of an ideal gas occupies 22.4 lit at STP. 2H I  H2 S O4  I2  S O2  2H2O


Volume of H2 gas formed at STP per mole of
HCl reacted is 22.4 × 0.5 litre. Sol.9 (C) CH2O
x+2–2=0
Sol.4 (B) From molecular formula of x=0
magnesium phosphate, it is evident that each
mole of Mg3 (PO 4 )2 contains 8 mole of oxygen Sol.10 (D) K 2Cr2O7  6KI  7H2SO 4 
atoms. 4K 2SO 4  Cr2 (SO 4 )3  7H2O  3I2
Therefore, 0.25 mole of oxygen atom will 3 3
0.25 C r2 (SO4 )3  2Cr  3SO42
remain present in mole i.e. 3.125  102
8
mole of Mg3 (PO 4 )2 . Sol.11 (C) Number of e transferred in each
case is 1, 3, 4, 5.
3
Sol.5 (A) 200 mg of CO2 = 200  10  0.2 g
Sol.12 (D)
44g of CO2  6  1023 molecules (approx.) 0 1 0 2
Zn  2 Ag CN  2 Ag Zn(CN)2
6  1023 Reduction
0.2g of CO2   0.2
44 Oxidation

 0.0272  1023  2.72  1021 molecule


Sol.13 (A) 6MnO4  I   6OH 
Now, 1021 molecule are removed.
So remaining molecules  2.72  1021  1021 6MnO24  IO3  2H2O
 1021 (2.72  1)  1.72  1021 molecule
Now, 6.023  1023 molecules = 1 mol Sol.14 (A)
H
1  1.72  1021
1.72  1021 molecules 
|
23 H  O  P  OH, hence it is dibasic. It acts as a
6.023  10 
 0.285  10 2
 2.85  10 3 O
reducing agent also.
Sol.6 (C)

K 2Cr2O7  4H2SO 4  K 2SO 4  Cr2 (SO 4 )3


12/two atom 6/two atom
Change by 6

S 1.15
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Stoichiometry and Redox Reactions

EXERCISE – I JEE ADVANCED


NaOH + HCl NaCl + H2O
Mole Concept after this reaction NaOH left = 5 mole
FeCl3 + 3NaOH Fe(OH)3 + 3NaCl
Sol.1 4HCl + MnO2 MnCl2 + 2H2O + Cl2 1. 5
69. 6 gm after this reaction NaOH left
69.6 = 5 – (1. 5)3 = 0. 5 mole
69. 6 gm of MnO2 = mole
87 Volume after reaction = 15 + 5 + 50 = 70 litre
69.6 0.5
mole of HCl =  4 mole Normality =  7.142  103 N
87 70
69.6 2Fe(OH)3 Fe2O3 + 3H2O
weight of HCl =  4  35.5  116 gm
87 1.5
weight of Fe2O3 =  160 = 120 gm
Sol.2 3TiO2(s) + 4C(s) + 6Cl2(g) 2
4. 32 gm 5. 76 gm 6. 82 gm
0. 054 mole 0. 48 mole 0. 0960 mole
Sol.7 Oleum = H2S2O7 = H2SO4 + SO3
3TiCl4(g) +2CO2(g) + 2CO(g) H2SO4 + 2NaOH Na2SO4 + 2H2O
L. R. = Cl2 mole of NaOH = (26. 7)x (0. 4) m mole
So TiCl4 mole produced = 10.68 m mole
1 mole of H2SO4 = 5. 34 m mole
=  0.0960 = 0. 048 mole weight of H2SO4 = 0. 523 gm
2
weight of TiCl4 produced H2S2O7 = H2SO4 + SO3
x gram (0. 5 – x) gm
= 0. 048 × 190 = 9. 12 gm
SO3 + H2O H2SO4
Sol.3 2SO2(g) + O2(g) + 2H2O() 2H2SO4 (0.5  x)
=  98 gm
5. 6 mole 4. 8 moles 80
L. R. = SO2 (0.5  x)98
Total H2SO4 = x +  0.523
So H2SO4 mole obtained in maximum=5.6 80
mole 0.0895
x= ~ 0. 3977 gm
0.225
Sol.4 Na2CO3 = x gram 0.5  0.3977
Pure Na2CO3 = (0. 95)x gm % SO3 = ~ 20. 4%
0.5
Na2CO3 + 2HCl(acid) H2CO3 + 2NaCl Sol.8 HPh:- NaOH + HCl NaCl + H2O …(1)
mole of acid = (45. 6 mL) × (0. 235) Na2CO3 + HCl NaHCO3 + NaCl. . (2)
= 10.716 m mole after MeOH :-
Moles of Na2CO3 required = 5. 358 m mole NaHCO3 + HCl H2CO3 + NaCl …(3)
Weight of Na2CO3 required mole of HCl (when HPh) = 1. 75 m mole
= (0. 95)x 5. 358 (106) × 10–3 mole of HCl (when MeOH)
x = 0. 597 gm = 0. 25 m mole (extra added)
amount of NaHCO3 = 0. 25 m mole
Sol.5 BaCl2 = 12% amount of HCl required in (2) & (3)
Molecular weight of BaCl2. 2H2O = (0. 25)2 = 0. 5 m mole
= 208 + 36 = 244 amount of Na2CO3 = 0. 25 m mole
BaCl2 = 6 gm amount of NaOH = 1. 75 – (0. 25)
244 = 1. 5 m mole
BaCl2. 2H2O = 6  = 7. 038 gm
208 NaOH (in gram) = 1. 5 × 10–3 × 40
H2O = 42. 962 gm. = 0. 06 gm per 200 mL
Sol.6 NaOH mole = 50(0. 2) = 10 mole Na2CO3 (in gram) = 0. 25 × 10–3 × 106
HCl mole = 5 mole = 0. 0265 gm/200 mL
FeCl3 mole = 1.5 mole (acidic)

S 1.16
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Stoichiometry and Redox Reactions

3 0.0248
Sol.9. 2KO2(S) + H2O() 2KOH(S) + O % of Cl =  6.1%
2 2(g) 0.4066
0. 158 mole 0. 1 mole
L. R = KO2 Sol.14 CaCO3 + H2SO4 CaSO4 + H2CO3
0. 5 gm
moles of O2 formed
moles of CaCO3 = moles of H2SO4
3
=  0.158  0.1185 0.5
4 required =
63.5  60
Sol.10 CaCl2 + H2CO3 CaCO3 + 2HCl = 4. 048 × 10–3 mole
CaCO3 CaO + CO2 m litre of 0. 5M H2SO4 required
0. 959 gm 4.048
moles of CaO = 0. 017125 mole = ml
0.5
moles of CaCl2 = 0. 017125 mole = 8. 096 ml
mass of CaCl2 = (0. 017125) × 111
= 1. 9 gm Sol.15 H2SO4 + 2NaOH Na2SO4 + 2H2O
1.9 moles of NaOH
% of CaCl2 =  45%
4.22 1
= 15   1.5 m mole
10
Conc. H SO
2 4
Sol.11 C6H12O  C6H10 moles of H2SO4 required
100 gm 1.5
= = 0. 75 m mole
100 2
moles of cyclohexanol =
100 In 12 mL, mole of H2SO4 = 0. 75 m mole
= 1 mole 0.75
In 1 L, mole of H2SO4 = mole
mole of cyclohexene = 0. 75 mole 12
mass of cyclohexene = (0. 75) × 89 In 1 L, weight of H2SO4 required
= 61. 5 gm 0.75
=  98 gram = 6. 125 gm/L
12
Sol.12 2NaCl Na2SO4 (By Na = atom
balance) Sol.16 ethane (C2H6) 
monobromination

(0.95)250 wurtz
 n-butane (C H
4 10 )
pure NaCl mole = = 4. 059 mole reaction
23  35.5
2 C2H6 C4H10 (by carbon balance)
4.059
pure Na2SO4 =  (46  96) XV
2
let’s say volume of ethane = x lt
= 288. 24 gm
weight of C4H10
288.24  100
Na2SO4 (90% pure) = x 90 85
90 =    58  55
2  22.4 100 100
= 320.27 gm
x = 55. 53 lit.
Sol.13 AgCl  unreacted Sol.17 mole of HCl = 30 × 0. 25 m mole
(0.466  x)gm
= 7. 5 m mole
AgBr AgCl
x gm
let's say x fraction is K2CO3 so
x 7.5 x(0.5) (1  x)(0.5)
AgCl formed = × (1435) gm  10 3  
188 2 138 74
= 0. 763 x x ~ 96%
Total weight after reaction Sol.18 mass of solution of HCl
= 0. 4066 – x + 0. 763 x = 100 × 1. 18 gm = 118 gm
weight lost = (1 – 0. 763)x = 0. 0725 mass of HCl in solution = (0. 36) (118)
x = 0. 306 gm = 30. 6% = 42. 48 gm
weight of Cl in initial mixture 42.48
35.5 nHCl = mole of HCl =
= (0. 4066 – 0. 306) × = 0. 0248 gm 365
143.5

S 1.17
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Stoichiometry and Redox Reactions

= 1. 163 mole 0.858


=  0.003 mole
2KMnO4 + 16HCl 2KCl + 2MnCl2 286
1.163 mole
 192  102V 
+ 8H2O + 5Cl2 103     0.003
0.363 mole  200 
6Cl2 + 6Ca(OH)2  Ca(ClO3 )2 V = 4 ml
0.363 mole 0.0606 mole amount of sulphate ion in gm
+ 5CaCl2 + 6H2O 51  4
=  (96)  10 3
Ca(ClO3 )2 + Na2SO4 CaSO4 + 2NaClO3 200
0.0606 mole 0.1212 mole = 0. 097. 92 gm/30 mL
mass prepared of NaClO3 = 6. 528 gm/L
= 0. 1212 x molecular weight = 12. 911 gm N
2
Sol.21 Mg  MgO + Mg3N2
O2
Mg2
Sol.19 NaH2PO4 
 Mg(NH4)PO4. 6H2O
MgO + 2HCl  MgCl2  H2O
NH
4 x Meq. x
mole
1 2

 Mg2P2O7 (by P-balance)
2 Mg3N2  HCl  3MgCl2  2NH3
(60  x)Meq. (60  x)Meq. 60  x  60  x 
1.054 mole   mole
mole of Mg2P2O7 = 2  3 
224
–3
MgCl2  2NaOH  Mg(OH)2  2NaCl
= 4. 747 × 10  60  x  12Meq.
 x 
weight of NaH2PO4 = 2 × 4. 747 × 10–3 ×  2 

(Molecular weight) NH3 + HCl



 NH4 + Cl
= 1. 139 gm
initially 10 Meq. x mole
Sol.20 moles of HNO3 = 8 × 5 m mole after (10 – x) m mole 
= 40 m mole 

mole of HCl = 4. 8 × 5 m mole HCl + NH4  OH NH4OH + Cl


6 Meq. 6 Meq.
= 24 m mole
x 60  x 12
let's say volume of H2SO4 is Vml  
2 2 2
so mole of H2SO4 = 17V m mole
x=27.27%
moles of HNO3 in 30 ml (picked up from 2 lt. sol)
40 120 Sol.22 PV = nTRT
=  30  m mole
2000 200 (1) (40) = nT (0. 0821) (400)
moles of HCl in 30 ml (picked up from nT = Total mole = 1. 2180
24 72 7
2 lt. sol) =  30  m mole C2H6  O2 2CO2 + 3H2O
2000 200 2
x mole
moles of H2SO4 is 30 ml (picked up from 2 lt. sol)
17V 51V C2H4 + 3O2 2CO2 + 2H2O
=  30  m mole (1.218  x) mole
2000 200
Total moles of H+ from 30 ml solution mole of O2 required
120 72 102V 7 130
=   = x + 3(1. 218 – x) =
200 200 200 2 32
x = 0. 817 mole
 192  102V 
=   m mole mole fraction of
 200  1.218  0.817
C2H4 =  0.33
1 1.218
mole Na2CO3 . 10H2O = mole
286 mole fraction of C2H6 = 0. 67
2
mole of OH = mole (in 100 mL) 1
286 Sol.23 Pb(NO3 )2 

 PbO + 2NO2 + O2
2  0.429 x gm 2
mole of OH in 42. 9 mL =
2.86

S 1.18
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Stoichiometry and Redox Reactions

1 after 1–x 3–3x 2x


2NaNO3 
  Na2O + 2NO2 + O2
(5  x)gm 2 P(Molecular weight) = SRT
1(M. W. ) = (0. 497) × (0. 0821) (298)
 (5  x)  1  5  x 
     2 (x) Molecular weight = 12. 15 gm
 85  4  85  (2x)(17)  (3  3x)2  (1  x)28
= 12. 15
4  2x
Sol.24 3Pb(NO3 )2  Cr2 (SO 4 )3 3PbSO4
11.25 m mole 2.5 m mole
34x + 6 – 6x + 28 – 28x = 48. 63 –24. 31 x
24. 31x = 14. 63
+ 2Cr(NO3)3
x = 0. 602
L. R. = CrSO4
% composition by volume
So moles of PbSO4 formed
1  0.602 0.398
= 2. 5 m mole × 3 N2   = 14. 21%
4  2(0.602) 2.795
= 7. 5 m mole
H2 = 3(N2%) = 42. 86%
11.25  7.5
molar conc. of [Pb2 ]  2(0.602)
70 NH3   42.86%
2.795
= 0. 0536 M
We know average molecular weight = 12.15
(2  11.25)
molar conc. of [NO3 ]  So (1) (12. 15)
70
mass
= 0. 32 M = × (0. 0821) × (273)
22.4
2  2.5
[Cr3 ]   0.0714M mass = 12. 14 gm.
70

Sol.25 NaCl Sol.28 x(CH3)2SiCl2 + ZnOH ZnCl+
CaCl2 + Na2CO3 CaCO3 + 2NaCl nH2O + [(CH3)2SiO]n

CaCO3   CaO  CO2 volume of film
1.12gm = 6 × 10–10 × 300 × 1 × 3 m3
1.12 = 54 × 10–8 m3 = 0. 54 cm3
mole of CaO =  0.02 mole
56 mass of the film = 0. 54 gm
moles of CaCl2 = 0. 02 mole mole of [(CH3)2SiO]n =
0.54
weight of CaCl2 = 2. 22 gm n[30  28  16]
NaCl = 10 – 2. 22 = 7. 78 gm 0.54
mass of [(CH3)2SiCl2] =  (58  71)
% NaCl = 77. 8% 71
= 0. 941 gm.
Sol.26 (i) Fe2O3 + 2Al Al2O3 + 2Fe
(ii) mole ratio (to complete reaction) = 1 : 2 Sol.29 P4 +3O2 P4O6 …. (i)
mass ratio = 1 × (112 + 48) (2 × 27) P4 + 5O2 P4O10 …(2)
= 80 : 27 (i) P4 + 3O2 P4O6
2700 1–x 4–y
(iii) 2. 7 kg of Al = mole
27 P4 + 5O2 P4O10
= 100 mole x y
16000 5x = y
16 kg of Fe2O3 = mole
160 3(1 – x) = 4 – y
= 1000 mole 3 – 3x = 4 – 5x
L . R. = Al 1
x=
So energy released 2
100 5
= 200 ×  10000 unit y
2 2
P4O6 = P4O10 = 50%
Sol.27 N2 : H2 (mole) = 1 : 3
(ii) P4 + 3O2 P4O6
N2 + 3H2 2NH3
3–x 11–y
Initially 1 3a
P4 + 5O2 P4O10

S 1.19
www.plancess.com
Stoichiometry and Redox Reactions

x y x
1. 8 =  0.418 x = 61. 5 gm
5x = y 44.5
3(3 – x) = 11 – y = mass of AlCl3
9 – 3x = 11 – 5x mass of KNO3 = 124 – 97 = 27 gm
x=1 total mole = 0. 267 + 0. 460 + 0. 422
1 2 = 1. 149 mole
P4O10 = ; P4O6 =
3 3 1
Sol.32 CH3COCH3 + 3 CaOCl2  CHCl3 +x
(iii) P4 + 3O2 P4O6 2 (acetone) 2 30 gm
3–x 13–y 30
P4 + 5O2 P4O10 mole of CHCl3 =
119.5
x y By carbon balance
5x = y mole of acetone (ideally)
3(3 – x) = 13 – y 1 30
9 – 3x = 13 – 5x = 
2 119.5
x=2
as the yield is 75%
P4O6 = 2
so weight required
P4O10 = 1
30 100
=   (58) = 9. 7 gm

Sol.30 Cl– + AgNO3 AgCl + NO3 2  119.5 75

let's say V ml must be added Sol.33 Cu2O + x


weight of solution = (1. 04 V) gm let's assume total 100 gm is given
weight of AgNO3 = 0. 05×(1. 04 V)gm Cu = 66. 67 gm
(0.05)(1.04V) 66.67 1
moles of AgNO3 = 0=   16
173 63.5 2
minimum moles of Cl– (it will be case of more Oxygen (O) = 8. 4
molecular weight i. e. KCl) % Cu2O = 66. 67 + 8. 4 = 75%
0.3 0.3
=  Sol.34 Hg + I2 HgI2
39  35.5 74.5
(0.05)(1.04V) 0.3  M   M x
   x   
173 74.5  200   254 2 
V = 13. 4 ml. 2Hg + I2 Hg2I2
x
Sol.31 In 500 ml of NaOH x mole
2
Weight of solution = 1. 8 × 500
= 900 gm let’s say M gm is initially taken
M M x
So weight of NaOH = (0. 08) (900) x  
= 72 gm 200 254 2
72  54  1 x
mole of NaOH = = 1. 8 mole M  
40  200  254 2
moles of H+ = 18 mole  254 
on heating NaHCO3 CO2 + H2O M x
on C-balance nCO  nNaHCO  0.54 
2 3 x
18.6 (gm) Hg2I2 =  (200 + 127) × 2 = 327 x
mass of NaHCO3 =  (84) 2
44 HgI2(gm)
= 33. 50 gm  M   
254
18.6  x  =   x =   1 x
H+ = 1. 8 =  3 0  200   (0.54)(200) 
44  27  3(35.5)  × Molecular weight = (1. 351 × 454)x
HgI2 : Hg2I2 = 0. 532 : 1.

S 1.20
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Stoichiometry and Redox Reactions

Redox Reactions or lose electrons and can go to –2, 0, +2 or


Sol.1 (a) NaNO2 higher +6 oxidation state.
Na+ Nx+ 2O2– (b) Oxidation state of oxygen in H2O2 is ‘–1’ so
+1+x–4=0 it can get oxidised or reduced because O have
x = +3 multiple oxidation state like –2, –1, 0. By losing
electrons it can form O2 and act as a reducing
(b) H2
agent and by gaining es , it can form H2O and
2x = 0
behave as an oxidising agent.
x=0
(c) Cl2O7
Sol.8 5 moles of H2SO4 can produce
2x – 14 = 0
1 mole of H2S
x = +7
0. 2 × V × 10–3 = nH2SO4
(d) KCrO3Cl
(equating equivalents)
K+ Crx+ 3O2– Cl–
Volume = 25 lit.
+1+x–6–1=0
x  6 Sol.9 20 × 0. 2 × 2 = 0. 167 M
(e) Ba Cl2 Normality = nf × M = 0. 5 N
+x–2=0
x  2 Sol.10
mole of As2O3 = 5. 54 × 10–4
(f) ICl3 equating equivalents,
+x–3=0 (5. 54 × 10–4)×(2) = (26. 1×10–3)×M×5
x  3 Molarity = 8. 49 × 10–3,
(g) K2Cr2O7 Normality = molarity × n-factor
+ 2 + 2x – 14 = 0 = (8. 49 × 10–3) × (5) = 4. 24 × 10–2
x  6
Sol.11 CaO CaC2O4
(h) CH2O +3 2 +4
CaC2O4 + KMnO4 CO2 + Mn2+
+x+2–2=0
+5e–
x 0
–2e–
(i) Ni (CO)4 Equating equivalents
+x+0=0 (equivalent) CaC O = (equivalent) KMnO
x=0 2 4 4

(j) NH2OH nCaC  2 = 40 × 0. 25 × 10–3


2O4
H+1 –2
Moles of CaC2O4 = 5 × 10–3
NO
mole of CaO = CaC2O4 = 5 × 10–3
H–1 H+1 mass of CaO = 0. 28
+3+x–2=0 % composition
0.28
x  1 =  100  54%
0.518

Sol.4 (a) Sulphur shows various oxidation Sol.12 Reaction


states such as –2, 0, +2, +4, +6 –1

In H2S, oxidation no. of S is ‘–2’


KMnO4 + H2O2 Mn2+ + O2
–5e–
So now it can only act as a reducing agent
because it can’t get more electrons since S2– is +2e–
in its lowest oxidation state. Assume mass of H2O2 = x gm
But in SO2 ,oxidation state of S is +4 which is molarity of
an intermediate oxidation state. So, it can gain

S 1.21
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Stoichiometry and Redox Reactions

x = 3. 21 × 10–3
 1000
34 Now,
H2O2 =  147 x M
20 moles of HCl = (moles of NH3) + (moles of NaOH)
0.316 50 × 0. 15 × 10–3 = 0. 2x + 3. 21 × 10–3
Moles of KMnO4 =  2  103
158 x = 2. 145 × 10–2
Now equating equivalents, molarity = 8x = 0. 1716 M
equivalents of H2O2 Sol.17
+7
= equivalents of KMnO4 KReO4 + Zn  Zn2  Re x
1. 47x × 20 × 10–3 × 2 = 2 × 10–3 × 5 +7
x = 0. 17 gm KMnO4
purity of H2O2 = 85% (i)
moles O2 evolved = moles of H2O2 consumed. +7

moles of O2 = 5 × 10–3 ReO4  Mn2


nRT moles of KReO4 = 9. 28 × 10–5
volume =  124.8 ml (ii)
P moles of KMnO4
= 0. 05 × 11. 45 × 10–3 × 5
Sol.13 (CaOCl)+ Cl– 5.7 gm is taken Now equating equivalents of
lets take moles of CaOCl2 = x Rex+ = KMnO4
molarity of (x x ) (7  x) = 5. 725 × 10–4 ……. (1)
Re
x
CaOCl2 =  1000  2x Now equating equivalents of
500
KReO4 = Rex+
Now on treatment with KI + HCl
9. 28 × 10–5 = Rex+ = x x 
(CaOCl)+Cl– + KI + HCl I2 Re
4
5.725  10
treated with 7 – x =
9.28  105
Na2S2O3
x =+1
equivalents of I2 = equivalents of Na2S2O3
1 Sol.18 Let moles of FeC2O4 = x
= 24. 35 × × 10–3 = 2. 435 milliequ.
10 FeSO4 = y
Now, equiv. of I2 = equiv. of Bleaching powder FeC2O4 + FeSO4 + KMnO4 Fe2+ + CO2
2. 435 × 10–3 = 2x × 25 × 10–3
x = 4. 87 × 10–2 Zn-dil HCl
mass of Bleaching powder = 1. 73 gm
1.73
% availability =  100 = 30. 33%
5.7 Fe+3
Sol.16
+5 –3
– KMnO4
NO3 + Mg(s) + H2O Mg(OH)

2(g) + OH (aq.) + NH3(g)
+8e
Fe+2
–2e–
NH3 + HCl NH4Cl Now, (2x + x + y) 0. 1 = 60 × 0. 02 × 5
 3x + y = 60
Say molarity of NO3 ions = x M x + y = 40 × 0. 02 × 5 = 4

moles of NO3 = x × 25 × 10–3 4 – x = 6 – 3x

2x = 2
Equivalents of NO3 x=1
= Equivalents of NH3 = 8 × x + 25 × 10–3 y=3
= 0. 2 x normality = 1 × 3 × 10–2 = 0.03N of FeC2O4
moles of NH3 = 0. 2 x = 3 × 10–2 = 0.03 M of FeSO4
moles of NaOH = 32. 10 × 10–3 × 0. 1

S 1.22
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Stoichiometry and Redox Reactions

Sol.19 mass of KCl = x gm So, 1 ml 0.1 millimole


H2O = 1 – x – y gm 40 ml 4 millimole
KClO3 = y gm Sol.21 BaCO3 + CaCO3 + CaO
treating with SO2 x y
+5
ClO3 + SO2SO24 + Cl–
+6e– dil. HCl
–2e–
CO2 HCO  7.5  10
3

Then silver chloride formed


2

x + y = 7. 5 × 10–3
total moles of chloride
BaCrO4 + I– I2 + Cr3+
x y
= 10–3 =  0. 1 x
74.5 122.5
Equating equivalents of BaCrO4 = I–
Now for another experiment
0. 1 x – 3 = 20 × 0. 05 × 10–3
FeSO4 102
x = 3. 33 × 10–3
30 × 0.2 × 10–3 3
y = 4. 167 × 10–3
Mass of BaCO3 = 0. 659 gm
CaCO3 = 0. 4167 gm
mass of CaO = 0. 1733
Reacted with Equivalent unreacted
% CaO = 13. 87%
KCl and KClO3 = 37.5 × 0.08 × 10–3

Equivalents reacted = 3 × 10–3 


Sol.22 Cu2S + CuS + MnO 4 
+5
ClO3  6Fe2  6H Cl– + 6Fe3++ 3H2O x y
+6e– 2+ 2+
Mn + Cu + SO2
+e– 3
200 × 0. 75 × 10–3 = 175  10
Equivalents of Fe2+ 5
= Equivalent of ClO3 
+ moles of required MnO 4
3 × 10–3 
moles required of MnO 4 = 0. 115
y
let moles of Cu2S–2 = x
= 122.5  10  25  10  6
3 3
CuS = y
25010
0. 115 × 5 = 8x + 6y
y = 0. 6125 gm
let m = mass of Cu2S

moles of ClO3 = 0. 005 8x + 6y = 0. 575
molar ratio = 1 : 1 8m 6(10  m)
  0.575
159 95.5
Sol.20 (iii) one ml of Na2S2O3 is equivalent to [(5. 03 × 10–2) – (6. 28 × 10–2)] m
0. 0499 gm of CuSO4 = – 5. 327 × 10–2
0. 2 millimole of CuSO4 m = 4. 26 gm
Since reaction is balanced 5.74
% CuS =  100  57.4%
Hg5(IO6)2 8I2 10
1 8
–4 o
5 × 10 4 millimole Sol.23 2H+ + O3 + I– O2 + I2 + H2O–2
2 CuSO4 I2
2 1 moles of air
0.2 millimole 0.1 millimole PV Na2S2O3
= 0.406 =
0.1 millimole of I2 equivalent to 0.2 RT
millimole of CuSO4
But we have 4 millimole

S 1.23
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Stoichiometry and Redox Reactions

Equivalents of I2 = 1. 5 × 10–3 × 0. 01 = 1. 5 × 2

8/3
10–5 Sol.27 MnSO4 .5H2O Mn3 O4
Moles of O3 = x 8/3
x × 6 = 1. 5 × 10–5 Now Mn3O4 + FeSO4  Fe3+ + Mn+2
x = 2. 5 × 10–6 + KMnO4
volume of O3 = 1. 847 × 10–4 lit. let assume no. of moles of
VO MnSO4 . 5H2O = x
3
% O3 = 1. 847 × 10–3 =  100 moles of Mn3O4 = 3x
10
3x(6)+100×0. 1×10–3 = 0. 12×100×10–3
 2
Sol.24 MnO4  H2C2O4  Fe  25 × N = 30 × 0. 1
30×1.5 1.5×0.5 15×0.4 N = 0. 12
Fe3  CO2  Mn2 x = 1. 11 × 10–4
mass of MnSO4. 4H2O = 1. 338 gm.
(30 × 1. 5) – (15 × 0. 5 + 15 × 0. 4)
= 31.5 milliequivalents 5
3  2 – 3
 31.5  10 Sol.28 (a) ClO3  Fe  Cl  Fe  H2O
final of MnO4 
60  103 5

= 0. 525 M 6H+ + ClO3 + 5e–  Cl– + 3H2O


final molarity of Fe+2  Fe+3 + e–× (5)

3+
15  0.4  103
Fe = 
6H++ ClO3 +5Fe2+5Fe3++Cl–+3H2O
60  103
= 0. 1 M (b) 8CuS–2 S8 + 16e– + 8Cu2+ ×(3)
5 2

final normalities MnO
3 4
 0.105M 4H++ NO3 +3e–  NO +2H2O ×(16)
Fe  0.1M

 
– –3 24CuS + 16NO3  64H 24Cu2+
Sol.25 (i) equivalents of I = 20 × 0. 1 × 10
1 2 + 3S8 + 16NO + 32H2O

H2 O2  I H2 O  I2 2
(c) S2O3  Sb2O5  SbO  H2SO3
equivalents of H2O2 = 2 × 10–3 6H+ + Sb2O5 + 6e–  2SbO + 3H2O
3
moles of H2O2 = 2  10  103
2 4
2 H2O + S2O32  2H2SO3 + 4e– + 2H+
3
Now, molarity = 10  103 = 0. 04 M 
25 2 
Sb2O5 + S2O3  4H 2SbO + 2H2SO3
Normality = 0. 04 × 2 = 0. 08 N
o  
(ii) 20 × 0. 3 × 10–3 = equivalent of I– (d) 2HCl–1  Cl2  2H  2e × (5)
20  0.3  103 7 2
Normality of H2O2= Fe + KMNO4 KCl + MnCl2

25  103
= 0. 24 + 4H2O × (2) + 8H+
strength = 1. 344 16HCl + 2KMnO4 5Cl2 + 2KCl +
2MnCl2 + 8H2O
5 7
Sol.26 Let molarity of Na2S2O3 solution = xM
(e) H2SO4 + KClO3  HClO 4 + 2e– + KHSO4
equivalent of thiosulphate
5 4
= Eq. of I– = Eq. of I2 = x × 45 × 10–3
3SO4+ KClO3  ClO2 + H2O + KHSO4
0.1
  5  x  45  103 
214
3KClO3 + 3H2SO4 3KHSO4 +
x  0.062 M HClO4 + 2ClO2 + H2O

S 1.24
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Stoichiometry and Redox Reactions

5 2
(f) 4H+ + HNO3 + 3e–  NO +
2H2O × (2)
1
2HBr  Br2 + 2e– + 2H+ × (3)

2HNO3 + 6HBr 2NO + 3Br2 + 4H2O
7 0
(g) H+ + 2IO 4 + 14e–  I2 + 4H2O
2I– I2 + 2e– × (7)

IO 4 + 7I– + 8H+ 4I2 + 4H2O
1
Sol.30 (a) H2O + 2e– + Ag2O 2Ag+ 2OH–
2 2
4OH– + S2O4  2SO3 + 2e– + H2O

S2O24 + Ag2O + 2OH– 2Ag
2
+ 2SO3 + H2O
o
(b) Cl2 + 2e– 2Cl–
o 1
Cl2 + 2OH–  2ClO + 2e– + 2H2O

Cl2 + 2OH Cl– + ClO– + H2O
0 1
(c) 2OH– + H2  H2O + 2e– + H2O × (3)
7 4
3e– + ReO4  ReO2 + 4OH– ×(2)


3H2 + 2ReO 4 2ReO2 + 2H2O + 2OH–
4 3
(d) ClO2 + e  ClO 2 –
×(2)
3 5
2H2O + SbO 2  Sb(OH)6 + 2e–
+ 2OH– + H2O


2ClO2 + SbO2 + 2OH– + 2H2O
 
 2ClO2  Sb(OH)6
7
(f) 4H2O+ MnO 4  5e  Mn+2+8OH–
Fe+2 Fe+3 + e– ×(5)

MnO 4 + 5Fe+2 + 4H2O Mn2+
+ 5Fe3+ + 8OH–

S 1.25
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Stoichiometry and Redox Reactions

EXERCISE – II JEE ADVANCED


1 1
Mole Concept It makes  mole of HNO2 & HNO3 till
2 2
Sol.1 A + Cl2 ACl2 1 1
reaction-III mole HNO2 make mole of
x y 2 6
M 71  M HNO3 in reaction-IV so HNO3 made
x y 1 1 2
 =  mole = mole
M 71  M 2 6 3
71x + Mx = My 1
71x 6 100 %
M % increase = 
xy 1 3
2
Sol.2 equivalents of H2SO4 = 1. 200 × 0. 2 (C) By above data, it is correct
= 0. 24 1 2
(D) mole of NO produced = 
moles of H2SO4 = 0. 12 2 3
mass of H2SO4 = 0. 12 × 98 = 11. 76 gm = 50 % of HNO3

Sol.3 NaI consumption per day 1


Sol.7 Initially mole of HCl = mole
0.5 2
=  3 gm = 0. 015 gm
100 1
= × Sol.36 5 gm = Sol.18 25 gm
0.015 2
number of I– =  6.023  1023
127  23 So after heating mole of HCl
= 6. 023 × 10+19 18.25  2.75 15.5
= = = 0. 424 mole
36.5 36.5
0.28 0.424
Sol.4 Statement-I : moles of N2 = normality = = 0. 5662 ~ 0. 58
28 0.750
= 0. 01 mole
PV = nRT Sol.8 Please note that, there is a small hypo in
At same P & T, V  n questions,
If M. W. = 44 gm of gas Instead of Ca(OH), it should be Ca(OH)2
n = 0. 01 mole Ca(OH)2 + 2HCl CaCl2 + 2H2O
Vn Moles of HCl = 0. 1 × 10 = 1m mole
So, volume will be same as moles are also Moles of Ca(OH)2 required
same = 0. 5 m mole
0.5
Volume = ml = 5 ml
Sol.5 We know that for isotopes 0.1
Mavg. = x(M1) + (1–x)M2
So statement-II is explaining statement-I and Sol.9 We know valency factor for Na2CO3 is 2
both are correct. 0.5
So molarity will be =  0.25M
2
Sol.6 (A) NH3 HNO3 + HNO2 (till reaction III) Sol.10 6. 90 N means in 1 lit. solution
by nitrogen balance KOH = 6. 90 moles
1 weight of KOH = 6. 90 × (56) = 386. 4 gm
nHNO  nNH
3 2 3 given 30% by weight is KOH
(B) 3HNO2 HNO3 + 2NO + H2O so weight of solution = 12. 88 gm
let's say 1 mole of NH3 is initially taken. 12.88
density =  1.288
1

S 1.26
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Stoichiometry and Redox Reactions

Sol.11 ferrous ammonium sulphate mole of Cl– in final solution


= FeSO4(NH4)2SO4. 6H2O = (0. 01 + 0. 02) × 2 = 0. 06
Molecular weight = 390
(0.1)(0.250) Sol.13 UF6 + xH2O UOxFy + gas (F6–y. H2x)
Moles in 0. 1 N, 250 mL = 3. 52gm 3. 08 gm 0. 8 gm
Valency factor
0. 01 mole
Fe2+ Fe3+ Valency factor = 1
gas contains 95% fluorine by mass
Mass of ferrous ammonium sulphate required
95
= (0. 1) (0. 250) (390) = 9. 8 gm = 0.8  = (6 – y) × 19
100
y = 5. 96
Sol.12 CuCl2  AgCl unreacted 5
(4.925 x)gm (5.74  y)gm 0.8   (2x)
100
CuBr2  2AgCl 2AgBr + CuCl2 x = 0. 02
x gm y gm
(A) so empirical formula F6–596 H2(0. 02)
let's say initially CuBr2 = x gm
= F0. 04 H0. 04
CuCl2 = 4. 925 – x gm
= HF
AgCl = y gram (reacts with reacted)
(B) empirical formula of solid = UOxFy
AgCl = 5. 74 – y gram (in reacted)
final reaction
Finally same AgCl AgBr & CuBr2
UF6 + BH2O UOxFy + A(HF)
CuCl2 (completely)
0. 01 0. 01
y
moles of AgCl in reaction = A = 2B (H-balance)
143.5
6 = Y + A (F - balance)
= mole of AgBr produced A
finally AgCl = (5. 74 – y) gm B=X= (O - balance)
2
y
AgBr =  (80  108) = y(1. 310) Y=6–A
143.5
UO A F6  A molecular weight
AgCl + AgBr = 6. 63 = 5. 74 + y(0. 310)
2
y = 2. 87 gm
3.08
so moles of =  308gm
0.01
2.87 x
CuBr2 =  A
2  143.5 223.5 238  (16) + (6 – A) × 19 = 308
2
x = 2. 235 gm
8A + 114 – 19A = 70
2.235
(A) CuBr2 mass % =  45.38% 11A = 44
4.925
A=4
(B) % mass of Cu =
So UO2F2
 2.235   4.925  2.235   63.5 A
    (C) % of F converted = = 66. 66%
 223.5   63.5  71   4.925 6
0.03  63.5
=  38.68%
4.925 1
Sol.14 Al5O12 molecular weight
(C) mole % of AgBr = 3
 2.87  = 267 + 135 + 196 = 598
  267
 143.5  (A) Y =  44.95%
= 50% 598
 2.87   9.74  2.87 
 
   135
 143.5   143.5  (B) Al =  22.57%
598
(D) moles of CuBr2 = moles of CuCl2 produced 196
= 0. 01 mole (C) O =  32.32%
598
moles of CuCl2 initially take
4.925  2.235
= = 0. 02 mole Sol.15 C6H8O6 molecular weight
134.5 = 72 + 8 + 96 = 176

S 1.27
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Stoichiometry and Redox Reactions

17.6 mg y = –2 + 5 = +3
moles of C6H8O6 = = 0. 1 m mole
176 Sol.2 The ore which get easily oxidised is best
(A) O – atom = 6 × nC  NA reducing agent
6H8O6
1
= 3. 6 × 1020 I–  I2 is most feasible because.
2
1
(B) mole = = 5. 68 × 10–3
176 Sol.3 Alumino thermite process :-
(C) moles of C6H8O6 = 0. 1 m mole Al + Mn3O4 Al2O3 + Mn

Sol.16 Volume strength Reducing agent
2H2O2() O2(g) + 2H2O()
5
1 lt. of H2O2 gives x lt. of O2 gas then X is said
Sol.5. ClO 3 + 6H+ + x Cl– + 3H2O
to be volume strength of H2O2

It X – V is given at S. T. P. then
6e– +5 –1
x
mole of O2 produced =
22.4
2
x Sol.6 [Fe(H2O)5(NO)+]–1 SO4
mole of H2O2 required= (in litre)
11.2 Fex+ 5(H2O)0 (NO)+
x x + 1 = +2
molarity =
11.2 x  1
x x
normality = × (valency factor) = 
11.2 5.6 Sol.7. KO2
x K  O2 2x = –1
Strength in g/L =  34
11.2
17x 1
=  x
5.6 2
Volume strength = Normality × 5. 6
0
2
Sol.17 (A) acid + acid No reaction Sol.8 3Br2  6CO3  3H2O 5Br– +
M1 V1  M2 V2 Total no of moles 5
Mavg. = = 6HCO3 + 5BrO3
V1  V2 Total volume
BrO Br–1 Reduction
Similarly (B)
BrO Br+5 Oxidation
(C) acid + basic 
M1 V1  M2 V2
Mavg. = Sol.9 H2O2 + KI I2
V1  V2
(×5)
(D) mili equivalent = x × M × Vml
moles M1 V1
(E) Molarity = =
volume Volume hypo
M1 V1 Sol.10 eq. of hypo solution eq. of I2
=
V2 20 × 0. 1 × 10–3 = 50 × 10–3 × NH O
2 2
moles mass (gm)  NH O  0.04
or =  2 2
volume Msolute  Volume (lt.)
concentration of H2O2
Redox Reactions in gm/lit. =
0.04
 34  0.34
2 4
Sol.1 N2H4 y = 10e–
each nitrogen coses 5e–
oxidation no. of N in

S 1.28
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Stoichiometry and Redox Reactions

Sol.11 MnO2 + HCl Cl2 8


Sol.18 Avg. oxidation no. of Pb3O4 is  . But
3
I– in reality, Pb3O4 is made up of PbO + PbO2 .So,
actively, Pb have oxidation state +2, +4.
I2 
hypo

Eq. of MnO2 + Eq. of hypo solution Sol.19 (1) Increase in oxidation no:- loss of
m electrons (oxidation)
 2  30  0.1  103 (2) Decrease in oxidation no :- gain of only e–s
87
m = 0. 1305 (reduction)
0.1305 (3) Oxidation agent :- gain of e–s
% =  100  26.1% (4) Reducing agent :- loss of e–s
0.5
(5) 2Cu+ Cu2+ + Cu
5+ – 3+ –e–
Sol.12 As + –2I As + I2
+2e +e–
–2e– Disproportionation reaction
valence factor = 5 for As (6) Redox reaction
2 for I (7) Mn3O4 oxidation no :-
8
 fractional
0  5 3
Sol.13 Cl2  Cl  ClO3

– (8) CH2Cl2
+e
x+2–2=0 zero oxidation no.
–5e– x=0
Disproportionation (9) NaOH + HCl  NaCl + H2O
(oxidation as well as reduction) Simple neutralisation reaction
0 2 1 5

Sol.14 I2  2S2O3  2I  S 4 O6


2  2
1

2 0 1

+e –5e– Sol.20 (a) O2  O2  O22
Disproportionation
2 4
Redox reaction
Sol.15 2H2S SO2  2H2O  3S
(b) CrO24  H  Cr2O72
tetrahedral dimeric bridged
–2e– +4e– tetrahedral ion

H2S S 0 – (–2) = +2 O O


SO2 S 0 – (4) = –4 || ||
Cr Cr
O– || O || O–
O
Sol.17 O O O O
||
| Cr |   
(c) MnO4  NO2  H  Mn2  NO3
O O tetrahedral trigonal
plonar
Valency of Cr is 6 all O have higher
electronegativity than Cr Redox Reaction
Cr’s oxidation no. = +6 O
||
OH– N
K2Cr2O7 K2CrO4 –
O O
H+
 2
orange Yellow (d) NO3  H2SO 4  Fe 
dichromate chromate Fe3+ + NO2 + H2O
Redox reaction

S 1.29
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Stoichiometry and Redox Reactions

PREVIOUS YEARS’ QUESTIONS JEE ADVANCED

Sol.1 Average atomic weight 69(5  x) NaNO


g 2
percentage of an isotope  atomic weight 85

100
 Residue: 222x  69(5  x)  3.6g
 10.81  10.01x  11.01(100  x) 330 85
100 x = 3.3 g Pb(NO3 )2
 x = 20%
Therefore, natural boron contain 20% (10.01)  NaNO3 = 1.7 g
isotope and 80% other isotope.
Sol.4 Compound B forms hydrated crystals with
Sol.2 From the vapour density information, Al2 (SO 4 )3 . Also, B is formed with univalent
Molar mass = vapour density × 2
metal on heating with sulphur. Hence,
( Molar mass of H2 = 2) compound B must have the molecular formula
= 38.3 × 2 = 76.6 M2SO 4 and compound A must be an oxide of
Now, let us consider 1.0 mole of mixture and it
M which reacts with sulphur to give metal
contains x mole of NO2 . sulphate as
 46x + 92 (1 – x) = 76.6 A  S M2SO 4
 x = 0.3348 B
Also, in 100 g mixture, number of moles
0.321 g sulphur gives 1.743 g of M2SO 4
100

76.6  32.1 g S (one mole) will give 174.3 g M2SO 4
 Moles of NO2 in mixture Therefore, molar mass of M2SO 4 = 174.3 g


100
 0.3348 = 0.437
 174.3 = 2 × Atomic weight of M + 32.1 + 64
76.6  Atomic weight of M = 39,
metal is potassium (K)
Sol.3 Heating below 600ºC converts Pb(NO3 )2 K 2SO 4 on treatment with aqueous Al2 (SO 4 )3
into PbO but to NaNO3 into NaNO 2 as: gives potash-alum.
 1 K2SO4  Al2 (SO4 )3  24H2O 
Pb(NO3 )2  PbO(s)  2NO2   O2  B
2
MW. 330 222 K2SO4 Al2 (SO4 )3 ·24H2O
C
 1
NaNO3  NaNO2 (s)  O2  If the metal oxide A has molecular formula MOx,
2
two moles of it combine with one mole of
MW.85 69
sulphur to give one mole of metal sulphate as
28
Weight loss  5   1.4 g
100 2KOx  S K 2SO 4
 Weight of residue left = 5 – 1.4 = 3.6 g  x = 2, i.e., A is KO 2 .
Now, let the original mixture contain x g of
Pb(NO3 )2 . Sol.5 93% H2SO 4 solution weight by volume

330 g Pb(NO3 )2 gives 222 g PbO indicates that there is 93 g H2SO 4 in 100 mL of

222 x solution.
x g Pb(NO3 )2 will give g PbO If we consider 100 mL solution, weight of
330
solution = 184 g
Similarly, 85 g NaNO3 gives 69 g NaNO 2
Weight of H2O in 100 mL solution
 (5 – x)g NaNO3 will give = 184 – 93 = 91 g

S 1.30
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Stoichiometry and Redox Reactions

Moles of solute 2
Change in oxidation number of Cr2 O7 per
 Molality   1000
Weight of solvent(g) 2
formula unit is 6 (it is always fixed for Cr2 O7 ).
93 1000
   10.43
98 91 Hence, equivalent weight of K 2Cr2O7
Molecular weight

Sol.6 Partial pressure of N2 = 0.001 atm, 6

T = 298 K, V= 2.46 dm3.


From Ideal Gas law : pV = nRT Sol.9 Na2S 4 O6 is a salt of H2S 4 O6 which has
pV 0.001  2.46 the following structure
n(N2 )    107 O O
RT 0.082  298 (0) (v)
 No. of molecules of N2 OH—S—S—S—S—OH
O O
 6.023  1023  107
 Difference in oxidation number of two
 6.023  1017
types of sulphur = 5.
Surface sites used in adsorption
20
  6.023  1017  2  6.023  1016 Sol.10 1. Both assertion and reason are factually
100
 Sites occupied per molecules true but the reason does not exactly explain the
assertion. The correct explanation is, methyl
Number of sites 2  6.023  1016 orange and phenolphthalein changes their
  2
Number of molecules 6.023  1016 colours at different pH.

Sol.7 The balanced chemical reaction is Sol.11 For the oxidation of An as:
3BaCl2  2Na3PO4  An  AO3 n-factor = 5 – n
Ba3 (PO 4 )2  6NaCl  Gram equivalent of An
= 2.68  103 (5 – n)
In this reaction, 3 moles of BaCl2 combined Now equating the above gram equivalent with
with 2 moles of Na3PO 4 . Hence, 0.5 mole of gram equivalent of KMnO 4 :
BaCl2 requires 2.68  103 (5  n)  1.61  10 3  5
2  n = +2
 0.5  0.33 mole of Na3PO 4 .
3
Sol.12 The redox reaction involved is :
Since available Na3PO 4 (0.2 mole) is less than
required mole (0.33), it is the limiting reactant H2O2  2I   2H  2H2O  I2
and would determine the amount of product If M is molarity of H2 O 2 solution, then
Ba3 (PO 4 )2 . 0.508  1000
5M 
2 moles of Na3PO 4 gives 1 mole Ba3 (PO 4 )2 254
( 1 mole H2O2  1 mole I 2 )
 0.2 mole of Na3PO 4 would give
 M = 0.4
1 Ba3 (PO 4 )2
 0.2 = 0.1 mole Also, n-factor of H2 O 2 is 2, therefore normality
2
of H2 O 2 solution is 0.8 N.
Sol.8 The following reaction occur between
 Volume strength = Normality × 5.6
S2O32 and Cr2O72 : = 0.8 × 5.6 = 4.48 V
26H 
 3S2O32  4Cr2O72 
6SO42  8Cr3  13H2O

S 1.31
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Stoichiometry and Redox Reactions

Sol.13 With KMnO 4 , oxalate ion is oxidized


only as:
5C2O42  2MnO4  16H 

2Mn2  10CO2  8H2O


Let, in the given mass of compound, x millimol
2
of C2O 4 ion is present, then
2 
Meq. of C2O 4 = Meq of MnO 4
 2x = 0.02 × 5 × 22.6
 x = 1.13
 2
At the later stage, with I ,Cu is reduced as :
2Cu2  4I   2CuI  I2
2  2
and I2  2S2O3  2I  S 4 O6
Let there be x millimole of Cu2 .
 Meq of Cu2 = Meq of I 2 = meq of hypo
 x = 11.3 + 0.05 = 0.565
 2
Meq of Cu2 : Meq of C2O 4
= 0.565 : 1.13 = 1 : 2

Sol.14 Let us consider 10 mL of the stock


solution contain x millimol oxalic acid H2C2O 4

and y millimol of NaHC2O 4 . When titrated


against NaOH, basicity of oxalic acid is 2 while
that of NaHC2O 4 is 1.
 2x + y = 3 × 0.1 = 0.3…(i)
When titrated against acidic KMnO 4 , n-factor

of both oxalic acid and NaHC2O 4 would be 2.


 2x + 2y = 4 × 0.1 = 0.4…(ii)
Solving equations (i) and (ii) gives y = 0.1, x =
0.1.
 In 1.0 L solution, mole of H2C2O 4
0.1
  100  0.01
1000
0.1
Mole of NaHC2O 4   100  0.01
1000

 Mass of H2C2O 4 = 90 × 0.01 = 0.9 g

Mass of NaHC2O 4 =112×0.01 = 1.12 g

S 1.32
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