Professional Documents
Culture Documents
Xrt-A
General Instructions:
In casee
This section consists of 25 multiple choice questions with overall choice to attempt any 20 questions.
considered for evaluation.
more than desirable numbers of questions are attempted,ONLY first 20 will be
substitution?
Which one of the following is most reactive towards nucleophilic
HC=CH-CCl2
S. CeHsC
CH-CH=CH-CI
D. CICH-CH=CH2
Which one among the following, reacts most readily with ethanol to form ethers?
2.
p-nitro benzyl bromide
P-chlorobenzyl bromide
C. p-methoxybenzyl bromide
The unit cell structure of a compound is shown below. The formula of the compound is
3.
AB2Cs
AB,C3
C. ABCs
D. ABCs
1|Page
closie
of these
electrical conductivity
shows Frenkel defects. The
and AgCl
Na shows Schottky defects
crystals is due to:
A. movement of ions and electrons
. movement of lons alone
movement of electrons alone
lower coordination number of NaCl.
side of the unit
.
Lithium metal crystallizes in a body- centered cubic crystal.
If the length of the
cell of lithium is 352pm, the atomic radius of the lithium will be
300.24 pm
B. 152.42 pm bet
C 158.2 pm
75.5 pm
6 The composition of a sample of Wustite is Fe0.930 and it shows metal deficiency defect.
What percentage of tho iron is present in the form of Fe (1) for the disappearance of 0.07 Fe ()
Ions?
5%
B
7.087
15.05 %
D. 23.60
What is the total volume of atoms in a face centred cubic unit cell of a metal? (ris atomic radius).
16/3 T
TTr
24/3 TT
D. 12/3 TT
D. 1> I1>
9) The structures of 4 alkyl halides are given below; which of the following is the incorrect
statement regarding the alkyl halides given.
21Page
10 This reaction would follow which of the
following pathway predominantly?
Acetone
SNT
CH-CH-CH-CH,Br+CH,CH,0 7
. SN2
Nucleophilic addition
D. Elimination reaction
11. Predict the major product in the following reaction:
Bromobutane+ Phenol - EtOK/anhvdrous Ethanol
OEt
A. Et
oPh
C. OPh
D.
12 From amongst the following alcohols the one that would react fastest with conc HCl and
anhydrous ZnClh, is
2-butanol
.
2-methylpropan-2-ol
2-methylpropanol
D. 1-butanol
13. The best reagent to convert Hex-3-en-2-ol into Hex-3-en-2-one is
MnOz
Pyridinium chlorochromate
Acidified KMnO4
D. Acidified K,CrO
14. ldentify the set of reagents/reaction conditions X and Y in the following set of transformations:
CH-CHCH;Br Product
CH-CH-CHs
X= aqueous NaOH, Y = HBr Br
X = alcoholic KOH, Y = HBr
X= aqueous KOH, Y = Br:/CHCl
15) In the hydroboration-oxidation reaction of propene with diborane, H,02 and NaOH, the
organic compound formed is:
CH,CH,OH
B CH,CHOHCH
CH, CHCH,OH
D. (CH),COH
3| Page
16. XeF is
&iv
i& Iv
9. Which of the
following is the
increasing order of
NH< PH,AsH enthalpy of
vaporization?
C
AsHa <PH<NH3
NH< AsHs PH <
D.
PH, AsHa< NH3
20 The total
Xa and Xa are thevapour pressure of a
binary
mole fractions of solution is
components A and B.given by: P
(75XA +360 Xa)=
41 Page
The solute is volatile.
The solution is a supersaturated with solute.
The solution is dilute
D. Solution must be formed from similar substances.
24. Non-ideal solutions showing positive deviations from Raoul's law
A. Acetone+ CHC
B. CHClh+ CeHe
C. H0+ HC
D. H,0+ CaH,OH
25. The mole fraction of the solute ina1 molal aqueous solution is:
A. 1
B. 1.8
. 18
D. 0.018
SECTION B
because of
26. DNA molecule is considered as a chiral molecule and shows optical activity
Nitrogenous bases
B. Deoxy ribose sugar
Ribose sugar
Phospho-ester bond.
The solubility of a gas in a liquid is directly proportional to the partial pressure of the gas present above
27.
the surface of liquid or solution.
28. The depression in freezing point of equimolal aqueous soltion wll be highest for
Ca (NOs2
5.
CeH120s
Urea
D. La (NO3)
29.
length is:
Forthe compounds CH,Cl, CH,Br, CHl and CH,F, the correct order of increasing C-halogen bond
CH F < CH,Cl < CH,Br < CH
A.
B.
CH,F< CH,Br < CH,Cl< CHl
5|Page
hemiacetal formation between
structure of glucose is due to
S0. Pyranose ring
A C1&C5
B C1&C4
& C3
c2 & C4 acid gives.
with concentrated nitric acid and sulphuric
Phenol, when reacts
S1
o-nitro phenol
p-ilrophenol
O-nitrophenol & p-nitrophenol
2,4, 6-trinitrophenol
2.
Amorphous solids are:
.
Anisotropic and super cooled liquids.
Isotropic and super cooled liquids.
5.
. 2-methyipentane
2, 2-dimethylbutane
2, 3-dimethyibutane
D. n-hexane
An example of an amino acid that has basic side chain:
Glycine
Gutamine
Lysine
D. Aspartic acid
2-methyl propan-2-ol
propan-1-ol
propan-2-ol
D. 2-methy! propan-1-ol
36. Ifthe dissolution process is endothermic (Asal H>0), the solubilty increases
With rise in temperature.
With decrease in temperature.
With the addition of more solute.
D. With the addition of more solvent.
In presence of NaOH, phenol reacts with CHC, to form o-hydroxy benzaldehyde. This reaction is
38.
called
6 1Page
Riemer-Tiemann's reaction
Sandmeyer's reaction
Kolbe's reaction
0. Gattermann's Koch synthesis
39. The units of 1 ppm are:
1 pg
A.
. 1 mg/g
mg
1 pgl
1 mg/Kg
CHs
CH,OH
CoHNH
CHNO2
wo statements labelled as Assertion (A) and Reason (R)
45. Given beloW ar
and dilute NaOH.
Assertion (A): Chlorine forms hypochlorite with cold
it disproportionate to form Chlorate and
Reason (R): Hypochlorite is unstable at high temperature,
chloride.
the options given below:
Select the most appropriate answer from
71Page
otA
A Both A and R are true and R is the correct explanation ofA.
B.
Both Aand Rare true but R is not the correct explanation
A is true but R is false.
D. A is false but R is true.
Given below are two statements labelled as Assertion (A) and Reason (R)
46
Assertion (A) The geometry of XeOaFa is seesaw shaped.
with three Oxygen atoms at equatorial position and
Reason (R): Xe undergoes SP d hybridization,
F-atoms at axial positions.
Select the most appropriate answer from the options given below
R are true and R is the correct explanation of A
A Both Aand
B. Both A and R are true but R is not the correct explanation of A.
A is true but R is false.
D. Als false but Ris true.
47 Given below are two statements labelled as Assertion (A) and Reason (R)
Assertion (A): Despite having an aldehydic group, Glucose does not react with NaHSOs
Reason (R): This reaction occurs in the presence of a free aldehyde group.
Select the most appropriate answer from the options given below
Both AA
and Rare true andbut
Risis not
R
the correct explanation of A
Both andRare true
A is true but R is false.
the correct explanation of A.
49 Given below are two statements labelled as Assertion (A) and Reason (R)
Assertion (A) : XeFs +3H,0- Xe0,+6HF is a redox reaction.
Reason (R): In the hydrolysis reaction given the hybridization of Xe does not change.
This section consists of 6 multiple choice questions with an overalchoice to allempt any 5. In case
more than desirable numbers of questions are attempted, ONLY first 5 will be considered for
evaluation.
8Page
50. Match the
following
A.HF
B. Covalency of
i. React with glass
N
C.XeF ii. Square pyramidal
D.BrFs iv. Distorted
E.HIL Octahedral
Which of the
following is the best matched option?
A-il, B-1, C-v, E-ii
B. A-v, B-1, C-i, D-il
C. A-ii, B-1, C-iv, D-ii
D. A-i, E-iv, D-ii, B-i
of this
For a molecule to taste sweet, it must bind to a receptor on a taste bud cell on the tongue. The binding
molecule causes a nenve impulse to pass from the taste bud to the brain, where the molecule is interpreted as
with the sweetness of glucose, the
being sweet. Sugars differ in their degree ot sweetness. Compared
Sweetness of sucrose is high, and that of fructose, the sweetest of all sugars. Developers of artificial sweetenet
must evaluatepotential products in terms of several factors-such as toxicily, stability and cost-in addition to
taste. Glucose, fructose and mannose are interconvertible carbohydrates through their keto enol isomerism.
The following questions are multiple cholice questions. Choose the most appropriate answer:
53. Look at the molecule given, which atom in the given molecule is anomeric carbon?
CHO
91Page
Atom B
B. Atom C
C. Atom D
D. Atom E
E. Atom F
54. Which name completely describes the above cyclic structure of compound?
A. a-D-Glucofuranose
B, B-D-Glucopyranose
C. a-D-Glucopyranose
D. B-D-Glucofuranose
****************