The amino group when attached to the ring makes it highly activating towards electrophilic substitution. Consequently, the electrophilic substitution readily takes place in aniline at all the three ortho and para positions. However on acetylation with acetyl chloride the activation of the ring to amino group is sufficiently reduced and the electrophilic substitution in benzene ring takes place preferably at the para position which is less hindered than the ortho position. Which of the following reagent is used to distinguish between

The amino group when attached to the ring makes it highly activating t

1.	The amino group when attached to the ring makes it highly activating towards electrophilic substitution. Consequently, the electrophilic substitution readily takes place in aniline at all the three ortho and para positions. However on acetylation with acetyl chloride the activation of the ring to amino group is sufficiently reduced and the electrophilic substitution in benzene ring takes place preferably at the para position which is less hindered than the ortho position. Which of the following reagent is used to distinguish between
Answer» Dilute `HCl` `C_(6)H_(5)SO_(2)Cl` and `OH^(-)//H_(2)O` `HONO` and `beta`-naphthol `AgNO_(3)` (AQUEOUS solution). Solution :HONO and `beta-`naphthol FORMS an azodye (COUPLING reaction) with `p-` toluidine while no reaction TAKES place for benzene amine