MCQEasyJEE 2025Amines (Classification & Properties)

JEE Chemistry 2025 Question with Solution

Identify correct statements: (A) Primary amines do not give diazonium salts when treated with NaNO2\text{NaNO}_2 in acidic condition. (B) Aliphatic and aromatic primary amines on heating with CHCl3\text{CHCl}_3 and ethanolic KOH\text{KOH} form carbylamines. (C) Secondary and tertiary amines also give carbylamine test. (D) Benzenesulfonyl chloride is known as Hinsberg’s reagent. (E) Tertiary amines react with benzenesulfonyl chloride very easily. Choose the correct answer from the options given below:

  • A

    (D) and (E) only

  • B

    (B) and (D) only

  • C

    (A) and (B) only

  • D

    (B) and (C) only

Answer

Correct answer:B

Step-by-step solution

Standard Method

Given: Five statements about amines, carbylamine test, diazotisation, and Hinsberg’s reagent are given.

Find: Which statements are correct and hence the correct option.

Analyze each statement one by one:

  1. (A) Primary amines do not give diazonium salts when treated with NaNO2\text{NaNO}_2 in acidic condition.

This is incorrect because aromatic primary amines form diazonium salts under these conditions. Therefore, (A) is false.

  1. (B) Aliphatic and aromatic primary amines on heating with CHCl3\text{CHCl}_3 and ethanolic KOH\text{KOH} form carbylamines.

This is the carbylamine reaction, which is given by primary amines. Therefore, (B) is true.

  1. (C) Secondary and tertiary amines also give carbylamine test.

This is incorrect because the carbylamine test is specific to primary amines only. Therefore, (C) is false.

  1. (D) Benzenesulfonyl chloride is known as Hinsberg’s reagent.

This statement is correct. Therefore, (D) is true.

  1. (E) Tertiary amines react with benzenesulfonyl chloride very easily.

This is incorrect because tertiary amines do not react with benzenesulfonyl chloride under mild conditions in the Hinsberg test. Therefore, (E) is false.

So, the correct statements are (B) and (D) only.

The correct option is B.

Statement-wise Analysis

Given: Statements (A) to (E) are based on reactions of amines.

Find: The combination of correct statements.

Step 1: Check diazotisation.

Primary aromatic amines react with NaNO2\text{NaNO}_2 in acidic medium to form diazonium salts, whereas aliphatic diazonium compounds are unstable. Hence statement (A) is incorrect.

Step 2: Check carbylamine test.

Primary amines on heating with CHCl3\text{CHCl}_3 and ethanolic KOH\text{KOH} give isocyanides or carbylamines. Hence statement (B) is correct.

Only primary amines respond to this test, so statement (C) is incorrect.

Step 3: Check Hinsberg reagent.

Benzenesulfonyl chloride is called Hinsberg’s reagent, so statement (D) is correct.

Tertiary amines do not react with benzenesulfonyl chloride because they do not have the required N–H bond. Hence statement (E) is incorrect.

Conclusion: The true statements are (B) and (D) only, so the correct option is B.

Common mistakes

  • Assuming all primary amines fail to form diazonium salts is incorrect because aromatic primary amines do form diazonium salts in acidic nitrite medium. Distinguish between aromatic and aliphatic primary amines before judging statement (A).

  • Treating the carbylamine test as common to all amines is wrong because it is specific to primary amines only. Use this test only for primary aliphatic or aromatic amines while evaluating statements (B) and (C).

  • Assuming tertiary amines react easily with benzenesulfonyl chloride is incorrect because they lack an N–H bond needed for the usual Hinsberg reaction. Check the structural requirement before marking statement (E) as true.

Practice more Amines (Classification & Properties) questions

Get unlimited AI-adaptive practice, mastery tracking, and an AI tutor that explains every step — free to start.

Related questions