Toluene is nitrated,and the resulting product | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(D) $1$. Nitration of toluene $(C_6H_5CH_3)$ gives a mixture of $o$-nitrotoluene and $p$-nitrotoluene.$2$. Reduction of these nitro compounds using $S

Vedclass · Accepted Answer

$O$ and $P$ bromotoluene

Vedclass · Answer

(D) $1$. Nitration of toluene $(C_6H_5CH_3)$ gives a mixture of $o$-nitrotoluene and $p$-nitrotoluene.$2$. Reduction of these nitro compounds using $Sn/HCl$ or $Fe/HCl$ yields $o$-toluidine and $p$-toluidine ($o$-methylaniline and $p$-methylaniline).$3$. Diazotization of these amines with $NaNO_2/HCl$ at $0-5 \ ^\circ C$ produces the corresponding diazonium salts ($o$-methylbenzenediazonium chloride and $p$-methylbenzenediazonium chloride).$4$. Heating these diazonium salts with cuprous bromide $(CuBr/HBr)$ (Sandmeyer reaction) replaces the diazonium group with a bromine atom,resulting in $o$-bromotoluene and $p$-bromotoluene.

Toluene is nitrated,and the resulting product is reduced. This is then diazotized and heated with cuprous bromide. What are the final products?

Similar Questions

Which of the following are intermediates in the Sandmeyer reaction?
$(i)$ $C_6H_5N^{+} \equiv NCl^{-}$
$(ii)$ $C_6H_5N^{+} \equiv N$
$(iii)$ $\overset{\centerdot }{C}_6H_5$
$(iv)$ $C_6H_5Cl$

Give the preparation of haloarenes from amine compounds.

Which among the following compounds is $NOT$ prepared by Sandmeyer's reaction?

Which of the following reactions uses a diazonium salt as a reactant?

Chlorobenzene is obtained from its corresponding diazonium salt by reaction with ......

Vedclass Test Series

Exam Paper Generator

Online Exam Module