JEE Exam  >  JEE Notes  >  Chemistry Main & Advanced  >  Amines: JEE Main Previous Year Questions (2021-2026)

Amines: JEE Main Previous Year Questions (2021-2026)

Download, print and study this document offline
Please wait while the PDF view is loading
 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: 
Read More

FAQs on Amines: JEE Main Previous Year Questions (2021-2026)

1. What are the different types of amines and how do I identify them in JEE questions?
Ans. Amines are classified as primary (RNH₂), secondary (R₂NH), and tertiary (R₃N) based on nitrogen's bonded carbon atoms. JEE questions often test identification through IUPAC nomenclature, basicity trends, and reactivity patterns. Primary amines show strongest basicity; tertiary amines show weakest. Recognising these distinctions helps solve previous year problems on amine synthesis and substitution reactions efficiently.
2. Why do some amines show stronger basicity than others in JEE Main exams?
Ans. Amine basicity depends on electron density at nitrogen and steric hindrance. Aliphatic primary amines are more basic than aromatic amines because benzene's π-electrons withdraw electron density from nitrogen. In JEE previous year questions, alkyl groups donate electron density, increasing basicity in the order: tertiary > secondary > primary (in aqueous solution). Hydrogen bonding effects also influence observed trends.
3. What are the common methods to prepare amines that repeatedly appear in JEE exams?
Ans. Major amine synthesis routes include reduction of nitriles (RCN → RCH₂NH₂), reduction of amides, and nucleophilic substitution of alkyl halides with ammonia or azide ions. Gabriel phthalimide synthesis produces primary amines selectively. Hofmann's exhaustive methylation and Cope elimination are elimination-based preparations. JEE examiners frequently test these mechanisms across 2021-2026 question papers.
4. How should I approach amine reaction questions involving electrophilic aromatic substitution?
Ans. Aromatic amines undergo electrophilic substitution faster than benzene due to nitrogen's +M (mesomeric) effect, which activates the ring and directs incoming groups to ortho and para positions. JEE previous year questions test this reactivity in nitration, sulphonation, and halogenation reactions. The amine group's strong activation means multiple substitutions occur readily, requiring careful mechanistic understanding.
5. What does the Hofmann elimination reaction teach us about amine structure in JEE Chemistry?
Ans. Hofmann elimination converts quaternary ammonium salts into alkenes and tertiary amines through successive methylation and heating. This reaction reveals amine basicity, reveals regioselectivity (produces less substituted alkenes), and distinguishes primary amines from secondary and tertiary types. JEE examiners use this transformation to test nitrogen reactivity, substitution patterns, and mechanistic reasoning across previous year question sets.
Explore Courses for JEE exam
Related Searches
Objective type Questions, Free, past year papers, ppt, Exam, Semester Notes, Important questions, Amines: JEE Main Previous Year Questions (2021-2026), Viva Questions, Summary, pdf , study material, video lectures, shortcuts and tricks, Amines: JEE Main Previous Year Questions (2021-2026), Previous Year Questions with Solutions, Amines: JEE Main Previous Year Questions (2021-2026), MCQs, Sample Paper, Extra Questions, practice quizzes, mock tests for examination;