Question Error Report

Thank you for reporting, we will resolve it shortly

Back to Question

Q. Mark the correct route of the conversion of $p$-chloroaniline to $p$-chlorobenzylamine.
image
(i) (ii) (iii)
(a) Alkylation $KCN$ $H_2/Pt$
(b) Diazotisation $CuCN$ $H_2/Pt$
(c) Oxidation $H_2/Pt$ Hydrolysis
(d) Diazotisation $H_2O/H^+$ $Sn/HCl$

Amines

Solution:

$P$-chloro aniline is diazotised to diazosalt, which reacts with $CuCN$ (sandmayer's reaction) to form $p$-chloro cyanobenzene, which in turn reacts with $H _{2} / Pt / Ni$ to form $p$ chloro benzylamine.
image