Explain the chemical reactions of benzene-diazonium chloride.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) The chemical reactions of diazonium salts are broadly classified into two categories: $(A)$ reactions involving the displacement of nitrogen and $(B)$ reactions involving the retention of the diazo group.
$(a)$ Reactions involving displacement of nitrogen:
The diazonium group is an excellent leaving group and is substituted by other groups such as $Cl^-$,$Br^-$,$I^-$,$CN^-$,and $OH^-$. The nitrogen gas $(N_2)$ is evolved during these reactions.
$(i)$ Sandmeyer reaction:
Nucleophiles like $Cl^-$,$Br^-$,and $CN^-$ can be introduced into the benzene ring by treating the diazonium salt solution with the corresponding cuprous halide ($Cu_2Cl_2$,$Cu_2Br_2$) or cyanide $(CuCN)$ in the presence of the respective acid ($HCl$,$HBr$) or $KCN$.
$(ii)$ Gatterman reaction:
Chlorine or bromine can be introduced into the benzene ring by treating the diazonium salt solution with the corresponding halogen acid in the presence of copper powder. This is known as the Gatterman reaction.

Explore More

Similar Questions

The reaction of $N,N'$-diphenylthiourea with concentrated $HCl$ upon heating is given by:
$(C_6H_5NH)_2C=S \xrightarrow{conc. HCl, Heat} A + B$
The unknown compounds $A$ and $B$ in the above reaction are:

What are $X$ and $Y$ in the following reactions?

$C_2H_5Br$ $\xrightarrow{AgCN} X$ $\xrightarrow{Reduction} Y$. Here,$Y$ is:

$CH_3NH_2 + CHCl_3 + KOH \rightarrow$ Nitrogen containing compound $+ KCl + H_2O$. The nitrogen-containing compound is:

Which of the following conjugate bases is stabilized to a greater extent due to solvation of ammonia and amines?

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo