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SECTION : A
Read the given passage and answer the questions number 1 to 5 that follow : [1 x 5 = 5]
The substitution reaction of alkyl halide mainly occurs by S N1 or SN2mechanism. Whatever mechanism alkyl halides
follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution
reactions. The rate of SN1 reactions are governed by the stability of carbocation whereas for S N2 reactions steric factor is
the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic
mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with HI is also governed by
steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in
deciding the kind of product formed.
1. Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes [1]
substitution reaction by SN1 mechanism.
2. Name the instrument used for measuring the angle by which the plane polarised light is rotated. [1]
3. Predict the major product formed when 2-Bromopentane reacts with alcoholic KOH. [1]
4. Write any one use of CHI3 [1]
5. Write the structures of the products formed when anisole is treated with HI. [1]
Questions number 6 to 10 are one word answers : [1 x 5 = 5]
6. Identify which liquid will have a higher vapour pressure at 90C if the boiling points of two [1]
liquids A and B are 140C and 180C, respectively.
7. Define the term Fuel cell [1]
8. How many of the following statements are incorrect statement. [1]
(a) Corrosion of iron can be minimized by forming contact with another metal with a
higher reduction potential.
(b) Iron corrodes in oxygen-free water.
(c) Corrosion of iron can be minimized by forming an impermeable barrier at its surface.
(d) Iron corrodes more rapidly in salt-water because its electrochemical potential is higher.
(e) Conductivity always increases with decrease in the concentration of electrolyte.
9. In the process of wine making, ripened grapes are crushed so that sugar and enzyme should [1]
come in contact with each other and fermentation should start. What will happen if anaerobic
conditions are not maintained during this process?
10. Write the IUPAC name of a secondary allylic alcohol of lowest number of carbon atom ? [1]
(1) P.T.O.
Questions number 11 to 15 are multiple choice questions
11. Phenol and ethanol may be distinguished with which reagent : [1]
(a) NaOH (aq.) (b) Neutral FeCl3 (c) H2/Ni (d) NaHCO3
12. Iodoform test is not given by : [1]
(a) Ethanol (b) Pentan-2-ol (c) methanol (d) isopropyl alcohol
13. For a cell reaction involving a two-electron change, the standard e.m.f. of the cell is found to be [1]
0.295 V at 25°C. The equilibrium constant of the reaction at 25°C will be:
(a) 1 × 10–10 (b) 29.5 × 10–2 (c) 10 (d) 1 × 1010
14. The most suitable reagent for the conversion of [1]
RCH2OH RCHO is :
(a) KMnO4 (b) K2Cr2O7
(c) CrO3 (d) PCC (pridine chlorochromate)
15. Conductivity (unit Siemen’s S) is directly proportional to the area of the vessel and the [1]
concentration of the solution in it and is inversely proportional to the length of the vessel then
the unit of the constant of proportionality is
(a) Sm mol-1 (b) Sm2 mol-1 (c) S-2m2 mol1 (d) S2m2 mol1
For questions number 16 to 20, two statements are given, one labelled Assertion (A) and the other
labelled Reason (R). Select the correct answer to these questions from the codes (i), (ii), (iii) and (iv) as
given below : [1 x 5 = 5]
(i) Both Assertion (A) and Reason (R) are correct statements, and Reason (R) is the correct explanation
of the Assertion (A).
(ii) Both Assertion (A) and Reason (R) are correct statements, but Reason (R) is not the correct
explanation of the Assertion (A).
(iii) Assertion (A) is correct, but Reason (R) is incorrect statement.
(iv) Assertion (A) is incorrect, but Reason (R) is correct statement.
16. Assertion: C2H5OH is a weaker base than phenol but is a stronger nucleophile than phenol. [1]
Reason: In phenol the lone pair of electrons on oxygen is withdrawn towards the ring due to
resonance.
17. Assertion: Aquatic species are more comfortable in cold waters rather than in warm waters. [1]
Reason: Different gases have different KH values at the same temperature
18. Assertion: Nitric acid and water form maximum boiling azeotrope. [1]
Reason: Azeotropes are binary mixtures having the same composition in liquid and vapour phase.
19. Assertion (A) : Alcohols have higher boiling point than alkanes of comparable molecular mass. [1]
Reason (R) : Alcohols have intra-molecular hydrogen bond.
20. Assertion (A) : Molality of a solution in liquid state changes with temperature. [1]
Reason (R) : The volume of solution changes with the change in temperature.
SECTION : B
21. What happens when – (1 x 2 = 2) [2]
(a) Propanone is treated with methylmagnesium iodide and then hydrolysed ?
(b) Benzene is treated with CH3COCl in presence of anhydrous AlCl3?
22. For a 5% solution of urea (Molar mass = 60 g/mol), calculate the osmotic pressure at 300 K. [2]
[R = 0·0821 L atm K–1mol–1] 2
OR
Visha took two aqueous solutions — one containing 7·5 g of urea (Molar mass = 60 g/mol) and
the other containing 42·75 g of substance Z in 100 g of water, respectively. It was observed that
both the solutions froze at the same temperature. Calculate the molar mass of Z.
(2) P.T.O.
23. Write the products of electrolysis in each of the following : (1 x 2 = 2) [2]
(a) An aqueous solution of CuSO4 with Pt electrode
(b) An aqueous solution of AgNO3 with Pt electrode
24. Write the major product obtained when t-butyl bromide reacts with sodium methoxide. Also, [2]
give its IUPAC name.
OR
(a) Show the chemical reaction with bond movements and arrows for the nucleophilic attack
of water on carbocation in acid catalysed hydration of alkenes.
(b) Give IUPAC name for the following :
30. Calculate the freezing point of a solution containing 0.5 g KCl (Molar mass = 74.5 g/mol) [3]
dissolved in 100 g water, assuming KCl to be 92% ionized. Kf of water = 1.86 K kg / mol.
(3) P.T.O.
31. Calculate the emf of the following cell at 298 K [3]
Cr(s) / Cr3+ (0.1 M) // Fe2+ (0.01 M) / Fe(s)
[ given is E0 of Fe2+/Fe=-0.44V and E0of Cr3+/Cr=-0.74V ]
OR
The e.m.f. of the following cell at 298 K is 0.1745
Fe (s)/ Fe2+ (0.1 M) // H+ (x M)/ (g) (1 bar)/ Pt (s)
0
Given : EFe 2
/ Fe
0.44V
32. How will you carry out the following conversions: [3]
i) Benzyl alcohol to phenyl ethanoic acid
ii) Propanone to propene
iii) Benzene to m-Nitroacetophenone
33. Write the chemical equations for following reactions : [3]
(i) Williamson’s synthesis
(ii) Kolbe reaction
(iii) Sandmeyer reaction
34. The freezing point of benzene decreases by 2.12 K when 2.5 g of benzoic acid (C6H5COOH) is [3]
dissolved in 25 g of benzene. If benzoic acid forms a dimer in benzene, calculate the van’t Hoff
factor and the percentage association of benzoic acid. (Kf for benzene = 5.12 K kg mol-1 )
35. a) Write the structural formula of A, B, C and D in the following sequence of reaction : [5]
(iii) Out of SN1 and SN2, which reaction occurs faster in polar protic solvent and why ?
36. (a) Calculate Gº for the reaction [5]
2 2
Zn (s) Cu Zn (aq) Cu (s).
Given : E o for Zn2+/Zn = – 0.76 V and
E o for Cu2+/Cu = + 0.34 V
R = 8.314 JK–1 mol–1
F = 96500 C mol–1.
(b) Give two advantages of fuel cells.
OR
(4) P.T.O.
(a) Out of the following pairs, predict with reason which pair will allow greater conduction
of electricity : (1 3 = 3)
(i) Silver wire at 30C or silver wire at 60C.
(ii) 0·1 M CH3COOH solution or 1 M CH3COOH solution.
(iii) KCl solution at 20C or KCl solution at 50C.
(b) Give two points of differences between electrochemical and electrolytic cells
37. (a) Out of t-butyl alcohol and n-butanol, which one will undergo acid catalyzed dehydration [5]
faster and why ? (2)
(b) Explain the following giving one example for each : (1 3 = 3)
(i) Reimer-Tiemann reaction.
(ii) Friedel-Craft’s acetylation of anisole.
(iii) Hydroboration oxidation of propene
OR
(a) Give the mechanism for the formation of ethanol from ethene. (2)
(b) Predict the reagent for carrying out the following conversions : (1 3 = 3)
(i) Phenol to benzoquinone
(ii) Anisole to p-bromoanisole
(iii) Phenol to 2,4,6-tribromophenol
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(5) P.T.O.