12 Chemistry23 24 sp01
12 Chemistry23 24 sp01
12 Chemistry23 24 sp01
Class 12 - Chemistry
Sample Paper - 01 (2023-24)
Maximum Marks: 70
Time Allowed: : 3 hours
General Instructions:
Section A
1. Which one of the following is employed as antityphoid drug?
a) Diphenyl hydramine
b) Chloramphenicol
c) Omeprazole
d) Chloroquine
2. ____ are joined together by phosphodiester linkage between 5′ and 3′ carbon atoms of the pentose sugar.
a) Nucleosides
b) Nucleic acids
c) Proteins
d) Nucleotides
3. In the following compounds:
a) x
b) x + y
c) x – y
d) Cannot be predicted with the equation
10. Which one of the following is used for the separation and purification of aldehydes
a) hydrogen cyanide
b) None of these
c) Grignard reagent
d) Sodium hydrogensulphite
11. Alcoholic compounds react:
a) only as nucleophiles.
Reason (R): The +I effect of alkyl groups (3 > 2 > 1 ) favours the dissociation of -OH group.
∘ ∘ ∘
OR
Calculate the mass of ascorbic acid (Vitamin C, C6H8O6) to be dissolved in 75 g of acetic acid to lower its melting point
Section C
22. a. The resistance of a conductivity cell containing 0.0001 M KCl solution at 298 K is 1500Ω . What is the cell constant
if the conductivity of 0.001 M KCl solution at 298 K is 0.146 × 10 S cm−3 −1
300 0.50
Calculate the rate constant.
(Given: log 2 = 0.3010, log 3 = 0.4771, log 4 = 0.6021)
24. Write the structures of the major products expected from the following reactions:
a. Mononitration of 3-methylphenoI
b. Dinitration of 3-methylphenol
c. Mononitration of phenyl methanoate
OR
Nitration is an example of aromatic electrophilic substitution and its rate depends upon the group already present in the
benzene ring. Out of benzene and phenol, which one is more easily nitrated and why?
25. How do you convert the following?
i. Benzoic acid to benzaldehyde.
ii. Ethyne to ethanal.
iii. Acetic acid to methane.
26. In the button cell, widely used in watches, the following reaction takes place
(aq) Given that
2+ −
Zn (s) + Ag O (s) + H O (l) → Z n
2 2 (aq) + 2Ag (s) + 20H
Θ Θ
E +
= 0.80V , E 2+
= −0.76 V
(Ag /Ag) (Zn /Zn)
Calculate standard emf and standard free Gibbs energy of the cell.
27. i. What is meant by chirality of a compound? Give an example.
ii. Which one of the following compounds is more easily hydrolysed by KOH and why? CH3CHClCH2CH3 or
CH3CH2CH2CH2Cl
Given: E 0
Zn
2+
/Zn
= −0.763V
and E 0
cu
2+
/cu
= +0.34V
Section D
29. Read the text carefully and answer the questions:
The d-block of the periodic table contains the elements of the groups 3 to 12 and are known as transition elements. In
general, the electronic configuration of these elements is (n - 1)d1-10 ns1-2. The d-orbitals of the penultimate energy level
in their atoms receive electrons giving rise to the three rows of the transition metals i.e. 3d, 4d and 5d series. However,
Zn, Cd and Hg are not regarded as transition elements. Transition elements exhibit certain characteristic properties like
variable oxidation stables, complex formation, formation of coloured ions, alloys, catalytic activity etc. Transition metals
are hard (except Zn, Cd and Hg) and have a high melting point.
i. Why are Zn, Cd and Hg non-transition elements?
OR
OR
OR
CoSO4Cl.5NH3 exists in two isomeric forms ‘A’ and ‘B’. Isomer ‘A’ reacts with AgNO3 to give white precipitate but
does not react with BaCl2. Isomer ‘B’ gives a white precipitate with BaCl2 but does not react with AgNO3. Answer the
following questions.
i. Identify ‘A’ and ‘B’ and write their structural formulas.
ii. Name the type of isomerism involved.
iii. Give the IUPAC name of ‘A’ and ‘B’.
33. i. Write the structure of main products when aniline reacts with the following reagents :
a. Br2 water
b. HCl
c. (CH3CO)2O/pyridine
ii. Arrange the following in the increasing order of their boiling point: C2H5NH2, C2H5OH, (CH3)3N
iii. Give a simple chemical test to distinguish between the following pair of compounds : (CH3)2NH and (CH3)3N.
OR
i. Give reasons:
a. Although – NH2 group is o/p directing in electrophilic substitution reactions, yet aniline, on nitration gives good
yield of m-nitroaniline.
b. (CH3)2 NH is more basic than (CH3)3 N in an aqueous solution.
c. Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
ii. Distinguish between the following:
a. CH3CH2NH2 and (CH3CH2)2 NH
b. Aniline and CH3NH2
Class 12 - Chemistry
Sample Paper - 01 (2023-24)
Solution
Section A
1. (b) Chloramphenicol
Explanation: Chlorine containing antibiotics, chloramphenicol, produced by soil microorganisms is very effective for
the treatment of typhoid fever. Chloramphenicol is an antityphoid drug.
2. (d) Nucleotides
Explanation: When nucleoside is linked to phosphoric acid at 5′-position of sugar moiety, we get a nucleotide and
nucleotides are joined by a phosphodiester bond between 5′ and 3′ carbon atoms of the pentose sugar.
3. (c) (iv) > (iii) > (i) > (ii)
Explanation: (iv) > (iii) > (i) > (ii)
4. (b) Acrolein
Explanation:
4.606×1000
= = 2
2.303×2×500
K2 2
= 10
K1
K2=100 times K1
6. (d) (a) - (ii), (b) - (iv), (c) - (i), (d) - (iii).
Explanation: (a) - (ii), (b) - (iv), (c) - (i), (d) - (iii).
7. (c) Chloroquine
Explanation: Chloroquine is a synthetic halogen compound. It is used for the treatment of malaria.
8. (b) [Xe] 4f75d1 6s2
Explanation: Atomic no. 64 Gd: [Xe] 4f75d1 6s2
9. (b) x + y
Explanation: Order of reaction with respect to A is x and w.r.t to B is y so total order of reaction is x+y.
10. (d) Sodium hydrogensulphite
Explanation:
Aldehydes and ketones form bisulphite addition product with NaHSO3 while impurites does not on hydrolysis we get
pure aldehydes and ketones.
= 1.5 × 10 −3
%
= 119.5gmol −1
15
mol
6 −3
10 ×10 Kg
= 1.26 × 10 −4
m
OR
= 176 g mol-1
Lowering of melting point, ΔT f = 1.5 K
We know that:
Kf ×w2 ×1000
ΔTf =
M2 ×w1
Δ Tf ×M2 ×w1
w2 =
Kf ×1000
1.5×176×75
=
3.9×1000
= 5.076 g
Hence, 5.076 g of ascorbic acid is needed to be dissolved.
21. a. Increasing order of boiling point :- CH3CHO < C2H5OH < CH3COOH
b. IUPAC name - hydroxybenzaldehyde
Section C
22. a. At Anode:
2+ −
M g(s) → M g (aq) + 2e
At Cathode:
2+ −
Cu (aq) + 2e → C u(s)
0.0591 0.001
= +0.34V − (−2.37V ) − log
2 0.0001
0.0591
= 2.71V − log 10
2
= 2.71V - 0.0295V
= 2.6805 V
For free gibbs energy
ΔG = −nEF
= −2 × 2.6805 × 96500
= -517336.5 J mol-1
= -517.34 KJ mol-1
b. At cathode: 2H (aq) + 2e + −
→ H2 (g)
= 3.66 × 10-3s-1
24. The combined influence of -OH and -CH3 groups determine the position of the incoming group. Keeping in view that
both -OH and -CH3 are o- and p-directing groups, the following products are obtained:
a.
b.
c.
OR
Phenol is more easily nitrated than benzene because the oxygen of the -OH group in phenol contains lone pairs and then
showed + M effect, which increases the electron density at 0 and p-positions in the benzene ring as a result electrophiles
attacks at more faster than benzene Nitration which is an electrophilic substitution reaction takes place more readily
where the electron density is more.
25. i. Benzoic acid to Benzaldehyde
H2 O | T automensation ||
CH ≡ CH −−−−−−−−−→ C H = C H2 −−−−−−−−−→ H − C − C H3
Elhyn e (unstable) Ethanal
H2 SO4 /H gSO4
At Cathode:
− −
Ag2 O(s) + H2 O(l) + 2e → 2Ag(s) + 2OH (aq)
Here, n = 2
F = 96500 C mol-1
Θ −1
ΔG = −2 × 1.56 V × 96000 C mol
= -301080 J mol-1
= -301.08 kJ mol-1
Θ −1
∴ ΔG = −308.08 kJ mol
27. i. An object or molecule which is non-superimposable on its mirror image is called chiral and the property of being
chiral is known as chirality, e.g. lactic acid, CH3CH(OH)COOH
ii. C H 3 − C H − C H2 C H3 is more easily hydrolysed by KOH because this hydrolysis occurs through
|
Cl
SN1 mechanism and this alkyl halide forms a more stable 2° carbocation than CH3-CH2-CH2-CH2Cl which forms a
iii. as iodide ion is a better leaving group because of its larger size therefore, it undergoes SN2
reaction faster.
28. Zn(s) → Zn
2+
(aq) + 2e
−
2+ −
Cu (aq) + 2e → C u(s)
2+ 2+
Zn(s) + C u (aq) → Z n (aq) + C u(s)
= 37.326
2.206
log K =
0.0591
k = Antilog 37.326
37
= 2.118 × 10
Section D
29. i. It is because neither they nor their ions have incompletely filled d-orbitals.
OR
OR
NaCl is an electrolyte and gets dissociated to two ions (Na+ and Cl-) and exerts almost double osmotic pressure
than glucose which is a non-electrolyte and does not dissociate.
Section E
31. Attempt any five of the following:
1. Invertase
2. The two nucleotides are joined by phosphodiester linkage.
3. Primary structure of proteins tells about the sequence in which various amino acids are linked with each other.
4. Milk, carrot
5. The 2 strands of DNA are attached to each other by hydrogen bonds that connect the nitrogenous bases of one strand
to the bases of the other strand (this is called complementary base pairing) where Adenine pairs with Thymine by 2
hydrogen bonds and Guanine pairs with Cytosine using 3 hydrogen bonds.
While nucleotides of DNA are held together by Phosphodiester linkages. The structure of DNA holds the nucleotides
in place using phosphodiester bonds. A phosphodiester bond occurs when exactly two of the hydroxyl group in
phosphoric acid react with hydroxyl groups on other molecules to form two ester bonds. The phosphodiester bond is
the linkage between the 3' carbon atom of one sugar molecule and the 5 ' carbon atom of another, deoxyribose in
DNA.
6. The catalysts present in the living organisms which speed down or fastens down the process are known as
biocatalysts. Eg:- Hormones in our body.
7. The forces which are responsible for tertiary structure of proteins are hydrogen bonds, disulphide linkage,
vanderwalls and electrostatic forces of attraction.
32. i. When the identical groups are on the same side of the metal ion, it is cis-isomer. When they are on opposite sides of
the metal ion, it is trans-isomer.
ii.
a. Bidentate ligand has two donor atoms and can form two bonds whereas monodentate ligand has only one donor
atom and can form only one bond with the metal ion.
b. Diamminedichloridoplatinum(IV) chloride.
OR
CoSO4Cl.5NH3:
i. Isomer A reacts with AgNO3 but not with BaCl2, it shows that it has Cl ion outside the coordination sphere. Hence,
A = [CO(NH3)5SO4]CI
Isomer B reacts with BaCl2 but not with AgNO3, it shows that it has SO4- outside the coordination sphere
Hence, B = [CO(NH3)5Cl]SO4
ii. Type of isomerism - Ionization isomerism.
iii. IUPAC name of, A = Pentaamminesulphatocobalt (III) chloride and B = Pentaamminesulphatocobalt (III) sulphate.
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33. i. a.
b.
c.
ii. Increasing order of boiling point (CH3)3N < C2H5NH2 < C2H5OH Alcohols have a higher boiling point as compared
to that of amines because oxygen being more electronegative forms stronger hydrogen bond as compared to that of
nitrogen. In tertiary amine, there is no hydrogen bond formation due to the absence of H-atoms and hence, has the
lowest boiling point.
iii. (CH3)2NH and (CH3)3N are secondary and tertiary amines respectively. These are distinguished by Hinsberg's
reagent which gives sulphonamide with secondary amines and no reaction with tertiary amines. (CH3)2NH reacts
with benzene sulphonyl chloride to give N, N-dimethyl benzene sulphonamide, which is insoluble in alkali. The
OR
i. a. Nitration is carried out in acidic medium. In an acidic medium, aniline is protonated to form the anilinium ion
which is meta directing. That is why besides the ortho and para derivatives, a substantial amount of meta
derivative (m-nitroaniline) is also formed.
b. (CH3)2NH is a secondary amine and (CH3)3N is a tertiary amine. Tertiary amine due to the presence of three
alkyl groups is more hindered than secondary amine which has only two alkyl groups attached to it. Therefore
formation of ammonium ion is easier in secondary amine than the tertiary amine. Therefore, it makes secondary
amine less basic than the tertiary amine.
c. The ammonolysis of alkyl halide leads to the formation of the mixture of primary, secondary and tertiary amine
along with the formation of quaternary salt. It is very difficult to separate pure primary amine from this mixture.
Test CH3CH2NH2 (CH3CH2)2NH
ii. a.
Forms a foul-smelling
Carbylamine test (add chloroform and alcoholic KOH No reaction take place
compound (gives positive
to both the compounds separately in a test tube) (gives negative test)
test)