What is obtained by the reaction of toluene w | vedclass

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(D) The reaction of toluene with chlorine in the presence of iron (a Lewis acid catalyst) and in the absence of light is an electrophilic aromatic sub

Vedclass · Accepted Answer

$A$ mixture of $(o)$-chlorotoluene and $(p)$-chlorotoluene

Vedclass · Answer

(D) The reaction of toluene with chlorine in the presence of iron (a Lewis acid catalyst) and in the absence of light is an electrophilic aromatic substitution reaction (specifically,chlorination of the benzene ring).In this reaction,the methyl group $(-CH_3)$ on the benzene ring is an ortho/para-directing group.Therefore,the chlorine atom will substitute the hydrogen atoms at the ortho and para positions of the benzene ring.This results in the formation of a mixture of $o$-chlorotoluene and $p$-chlorotoluene.

What is obtained by the reaction of toluene with chlorine in the presence of iron and in the absence of light?

Similar Questions

$C_{6}H_{6} + CH_{3}Cl \xrightarrow{\text{Anhy. } AlCl_{3}} C_{6}H_{5}CH_{3} + HCl$
The name of the above reaction is:

Arrange the following compounds in decreasing order of their reactivity towards electrophilic substitution $(S_E)$ reaction: $I$. Chlorobenzene,$II$. Benzene,$III$. Anilinium chloride,$IV$. Toluene.

Assertion : Friedel-Craft's reaction is used to introduce an alkyl or acyl group in benzene nucleus.
Reason : Benzene is a solvent for the Friedel-Craft's alkylation of bromobenzene.

Oxidation of toluene with dilute $HNO_3$ gives:

The chemicals used for preparing acetophenone via Friedel-Crafts acylation are:
$(A)$ $C_6H_6$
$(B)$ $CH_3COCH_3$
$(C)$ $CH_3COCl$
$(D)$ Anhydrous $AlCl_3$

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