In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution.Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.

In the following question two Statement-I (Assertion) and Statement-2

1.	In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution.Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.
Answer» In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options: Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution. Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.