Assertion : 4-Nitrochlorobenzene undergoes nu | vedclass

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

Question

(A) The Assertion is correct because the presence of an electron-withdrawing $-NO_2$ group at the $para-$position stabilizes the carbanion intermediat

Vedclass · Accepted Answer

If both Assertion and Reason are correct and the Reason is a correct explanation of the Assertion.

Vedclass · Answer

(A) The Assertion is correct because the presence of an electron-withdrawing $-NO_2$ group at the $para-$position stabilizes the carbanion intermediate formed during nucleophilic aromatic substitution.The Reason is also correct. Chlorobenzene typically requires harsh conditions and proceeds via an elimination-addition mechanism (benzyne intermediate) due to the lack of electron-withdrawing groups. In contrast,$4-$nitrochlorobenzene undergoes nucleophilic aromatic substitution via an addition-elimination mechanism (Meisenheimer complex) because the $-NO_2$ group strongly activates the ring towards nucleophilic attack.Since the mechanism described in the Reason explains why $4-$nitrochlorobenzene is more reactive,the Reason is the correct explanation of the Assertion.

Assertion : $4-$Nitrochlorobenzene undergoes nucleophilic substitution more readily than chlorobenzene.
Reason : Chlorobenzene undergoes nucleophilic substitution by elimination-addition mechanism while $4-$nitrochlorobenzene undergoes nucleophilic substitution by addition-elimination mechanism.

Similar Questions

The most reactive compound towards nucleophilic substitution with an aqueous $NaOH$ is

The reaction of bromobenzene with bromomethane and sodium metal in dry ether to give toluene is known as:

The replacement of $Cl$ in chlorobenzene to form phenol requires drastic conditions,but the chlorine in $2,4-$dinitrochlorobenzene is readily replaced because:

Which of the following is the product of Fittig reaction?

Give chemical reactions for the following conversions:
$(1)$ Nitrobenzene from phenol
$(2)$ $p$-methylacetophenone from benzene

Vedclass Test Series

Exam Paper Generator

Online Exam Module

Assertion : $4-$Nitrochlorobenzene undergoes nucleophilic substitution more readily than chlorobenzene.Reason : Chlorobenzene undergoes nucleophilic substitution by elimination-addition mechanism while $4-$nitrochlorobenzene undergoes nucleophilic substitution by addition-elimination mechanism.