Page 1
JEE Main Previous Year Questions (2021-2026):
Amines
(January 2026)
Q1: A student performed analysis of aliphatic organic compound ‘X’ which on analysis
gave C = 61.01%, H = 15.25%, N = 23.74%.
This compound, on treatment with HNO
2
/H
2
O produced another compound ‘Y’ which did
not contain any nitrogen atom. However, the compound ‘Y’ upon controlled oxidation
produced another compound ‘Z’ that responded to iodoform test.
The structure of ‘X’ is:
A: CH
3
-CH
2
CH(NH
2
)-CH
3
B: CH
3
CH
2
CH
2
NH
2
C: Ph-CH(CH3)-NH
2
D:
Answer: D
Explanation:
Q2: Total number of alkali insoluble solid sulphonamides obtained by reaction of given
amines with Hinsberg's reagent is ________.
Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methyl
methanamine, Phenylmethanamine, N-propylaniline, N-phenylaniline,
N,N-Dimethylaniline, Allyl amine, Isopropyl amine
Page 2
JEE Main Previous Year Questions (2021-2026):
Amines
(January 2026)
Q1: A student performed analysis of aliphatic organic compound ‘X’ which on analysis
gave C = 61.01%, H = 15.25%, N = 23.74%.
This compound, on treatment with HNO
2
/H
2
O produced another compound ‘Y’ which did
not contain any nitrogen atom. However, the compound ‘Y’ upon controlled oxidation
produced another compound ‘Z’ that responded to iodoform test.
The structure of ‘X’ is:
A: CH
3
-CH
2
CH(NH
2
)-CH
3
B: CH
3
CH
2
CH
2
NH
2
C: Ph-CH(CH3)-NH
2
D:
Answer: D
Explanation:
Q2: Total number of alkali insoluble solid sulphonamides obtained by reaction of given
amines with Hinsberg's reagent is ________.
Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methyl
methanamine, Phenylmethanamine, N-propylaniline, N-phenylaniline,
N,N-Dimethylaniline, Allyl amine, Isopropyl amine
A: 8
B: 5
C: 2
D: 4
Answer: D
Explanation:
In Hinsberg’s test, the sulphonamide formed from a 2° (secondary) amine is alkali insoluble.
This is because a 2° amine has no N–H left in the sulphonamide, so it cannot form a soluble salt
with alkali.
So, we have to count the 2° amines from the given list.
Ph – NH – CH 3, Me – NH – Me,
Ph – NH – CH 2 – CH 2 – CH 3, Ph – NH – Ph
Q3: Given below are two statements:
Statement I : The dipole moment of R-CN is greater than R-NC and R-NC can
Statement II : R–CN hydrolyses under acidic medium to produce a compound which on
treatment with SOCl 2, followed by the addition of NH 3 gives another compound (x). This
compound (x) on treatment with NaOCl/NaOH gives a product, that on treatment with
CHCl 3/KOH/? produces R–NC
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are false
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are true
Answer: B
Explanation:
Page 3
JEE Main Previous Year Questions (2021-2026):
Amines
(January 2026)
Q1: A student performed analysis of aliphatic organic compound ‘X’ which on analysis
gave C = 61.01%, H = 15.25%, N = 23.74%.
This compound, on treatment with HNO
2
/H
2
O produced another compound ‘Y’ which did
not contain any nitrogen atom. However, the compound ‘Y’ upon controlled oxidation
produced another compound ‘Z’ that responded to iodoform test.
The structure of ‘X’ is:
A: CH
3
-CH
2
CH(NH
2
)-CH
3
B: CH
3
CH
2
CH
2
NH
2
C: Ph-CH(CH3)-NH
2
D:
Answer: D
Explanation:
Q2: Total number of alkali insoluble solid sulphonamides obtained by reaction of given
amines with Hinsberg's reagent is ________.
Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methyl
methanamine, Phenylmethanamine, N-propylaniline, N-phenylaniline,
N,N-Dimethylaniline, Allyl amine, Isopropyl amine
A: 8
B: 5
C: 2
D: 4
Answer: D
Explanation:
In Hinsberg’s test, the sulphonamide formed from a 2° (secondary) amine is alkali insoluble.
This is because a 2° amine has no N–H left in the sulphonamide, so it cannot form a soluble salt
with alkali.
So, we have to count the 2° amines from the given list.
Ph – NH – CH 3, Me – NH – Me,
Ph – NH – CH 2 – CH 2 – CH 3, Ph – NH – Ph
Q3: Given below are two statements:
Statement I : The dipole moment of R-CN is greater than R-NC and R-NC can
Statement II : R–CN hydrolyses under acidic medium to produce a compound which on
treatment with SOCl 2, followed by the addition of NH 3 gives another compound (x). This
compound (x) on treatment with NaOCl/NaOH gives a product, that on treatment with
CHCl 3/KOH/? produces R–NC
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are false
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are true
Answer: B
Explanation:
Q4: A student has planned to prepare acetanilide from aniline using acetic anhydride.
The student has started from 9.3 g of aniline. However, the student has managed to
obtain 11 g of dry acetanilide.
The % yield of this reaction is:-
A: 59.5%
B: 72.5
C: 97.5
D: 81.5%
Answer: D
Explanation:
Q5: The correct stability order of the following diazonium salts is
A: C > D > B > A
B: A > C > D > B
Page 4
JEE Main Previous Year Questions (2021-2026):
Amines
(January 2026)
Q1: A student performed analysis of aliphatic organic compound ‘X’ which on analysis
gave C = 61.01%, H = 15.25%, N = 23.74%.
This compound, on treatment with HNO
2
/H
2
O produced another compound ‘Y’ which did
not contain any nitrogen atom. However, the compound ‘Y’ upon controlled oxidation
produced another compound ‘Z’ that responded to iodoform test.
The structure of ‘X’ is:
A: CH
3
-CH
2
CH(NH
2
)-CH
3
B: CH
3
CH
2
CH
2
NH
2
C: Ph-CH(CH3)-NH
2
D:
Answer: D
Explanation:
Q2: Total number of alkali insoluble solid sulphonamides obtained by reaction of given
amines with Hinsberg's reagent is ________.
Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methyl
methanamine, Phenylmethanamine, N-propylaniline, N-phenylaniline,
N,N-Dimethylaniline, Allyl amine, Isopropyl amine
A: 8
B: 5
C: 2
D: 4
Answer: D
Explanation:
In Hinsberg’s test, the sulphonamide formed from a 2° (secondary) amine is alkali insoluble.
This is because a 2° amine has no N–H left in the sulphonamide, so it cannot form a soluble salt
with alkali.
So, we have to count the 2° amines from the given list.
Ph – NH – CH 3, Me – NH – Me,
Ph – NH – CH 2 – CH 2 – CH 3, Ph – NH – Ph
Q3: Given below are two statements:
Statement I : The dipole moment of R-CN is greater than R-NC and R-NC can
Statement II : R–CN hydrolyses under acidic medium to produce a compound which on
treatment with SOCl 2, followed by the addition of NH 3 gives another compound (x). This
compound (x) on treatment with NaOCl/NaOH gives a product, that on treatment with
CHCl 3/KOH/? produces R–NC
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are false
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are true
Answer: B
Explanation:
Q4: A student has planned to prepare acetanilide from aniline using acetic anhydride.
The student has started from 9.3 g of aniline. However, the student has managed to
obtain 11 g of dry acetanilide.
The % yield of this reaction is:-
A: 59.5%
B: 72.5
C: 97.5
D: 81.5%
Answer: D
Explanation:
Q5: The correct stability order of the following diazonium salts is
A: C > D > B > A
B: A > C > D > B
C: A > B > C > D
D: C > A > D > B
Answer: B
Explanation:
Correct order of stability
EDG increases stability
EWG decreases stability
Q6: Given below are two statements:
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are true
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are false
Answer: A
Explanation:
S t a t e m e n t - I
Page 5
JEE Main Previous Year Questions (2021-2026):
Amines
(January 2026)
Q1: A student performed analysis of aliphatic organic compound ‘X’ which on analysis
gave C = 61.01%, H = 15.25%, N = 23.74%.
This compound, on treatment with HNO
2
/H
2
O produced another compound ‘Y’ which did
not contain any nitrogen atom. However, the compound ‘Y’ upon controlled oxidation
produced another compound ‘Z’ that responded to iodoform test.
The structure of ‘X’ is:
A: CH
3
-CH
2
CH(NH
2
)-CH
3
B: CH
3
CH
2
CH
2
NH
2
C: Ph-CH(CH3)-NH
2
D:
Answer: D
Explanation:
Q2: Total number of alkali insoluble solid sulphonamides obtained by reaction of given
amines with Hinsberg's reagent is ________.
Aniline, N-Methylaniline, Methanamine, N,N-Dimethylmethanamine, N-Methyl
methanamine, Phenylmethanamine, N-propylaniline, N-phenylaniline,
N,N-Dimethylaniline, Allyl amine, Isopropyl amine
A: 8
B: 5
C: 2
D: 4
Answer: D
Explanation:
In Hinsberg’s test, the sulphonamide formed from a 2° (secondary) amine is alkali insoluble.
This is because a 2° amine has no N–H left in the sulphonamide, so it cannot form a soluble salt
with alkali.
So, we have to count the 2° amines from the given list.
Ph – NH – CH 3, Me – NH – Me,
Ph – NH – CH 2 – CH 2 – CH 3, Ph – NH – Ph
Q3: Given below are two statements:
Statement I : The dipole moment of R-CN is greater than R-NC and R-NC can
Statement II : R–CN hydrolyses under acidic medium to produce a compound which on
treatment with SOCl 2, followed by the addition of NH 3 gives another compound (x). This
compound (x) on treatment with NaOCl/NaOH gives a product, that on treatment with
CHCl 3/KOH/? produces R–NC
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are false
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are true
Answer: B
Explanation:
Q4: A student has planned to prepare acetanilide from aniline using acetic anhydride.
The student has started from 9.3 g of aniline. However, the student has managed to
obtain 11 g of dry acetanilide.
The % yield of this reaction is:-
A: 59.5%
B: 72.5
C: 97.5
D: 81.5%
Answer: D
Explanation:
Q5: The correct stability order of the following diazonium salts is
A: C > D > B > A
B: A > C > D > B
C: A > B > C > D
D: C > A > D > B
Answer: B
Explanation:
Correct order of stability
EDG increases stability
EWG decreases stability
Q6: Given below are two statements:
In the light of the above statements, choose the correct answer from the options given
below
A: Both Statement I and Statement II are true
B: Statement I is false but Statement II is true
C: Statement I is true but Statement II is false
D: Both Statement I and Statement II are false
Answer: A
Explanation:
S t a t e m e n t - I
Statement-II
Q7: A student has been given a compound "x" of molecular formula- C 6H 7 N. "x" is
sparingly soluble in water. However, on addition of dilute mineral acid, "x" becomes
soluble in water. "x" when treated with CHCl 3 and KOH(alc), 'y' is produced. 'y' has a
specific unpleasant smell. On treatment with benzenesulphonyl chloride, 'x’ gives a
compound 'z' which is soluble in alkali. The number of different H atoms present in 'z’ is:-
A: 8
B: 4
C: 5
D: 7
Answer: D
Explanation:
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