NEETChemistryAmines
Read the following statements regarding the electrophilic aromatic substitution reactions of aniline: (A) It does not undergo Friedel-Crafts alkylation due to salt formation with aluminium chloride. (B) Direct nitration yields a significant amount of m -nitroaniline. (C) The anilinium ion formed in strongly acidic medium is an activating group. (D) Monobromination requires protection of the - NH ₂ group by acetylatio
Options
- A(A), (B), (C) and (D)
- B(A) and (D) only
- C(B) and (C) only
- D(A), (B) and (D) only
Correct answer
D. (A), (B) and (D) only
Step-by-step solution
Statement (A) is correct: Aniline forms a salt with the Lewis acid catalyst ( AlCl ₃ ), which acts as a strongly deactivating group, preventing Friedel-Crafts reactions. Statement (B) is correct: During direct nitration in a strongly acidic medium, aniline is protonated to form the anilinium ion, which directs the incoming electrophile to the meta position, yielding about 47% m -nitroaniline. Statement (C) is incorrect: The anilinium ion ( - NH ₃^+ ) is a strongly deactivating group, not an activating group. Statem