Replacement of Cl of chlorobenzene to give ph | vedclass

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(D) The $-NO_2$ group is a strong electron-withdrawing group due to its $-I$ and $-M$ effects. In $2,4-$dinitrochlorobenzene,the $-NO_2$ groups are pr

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$NO_2$ withdraws $e^-$ from ortho$/$para positions.

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(D) The $-NO_2$ group is a strong electron-withdrawing group due to its $-I$ and $-M$ effects. In $2,4-$dinitrochlorobenzene,the $-NO_2$ groups are present at the ortho and para positions relative to the chlorine atom. These groups withdraw electron density from the ring,specifically stabilizing the carbanion intermediate formed during nucleophilic aromatic substitution. This makes the $C-Cl$ bond more susceptible to nucleophilic attack,thus facilitating the replacement of the chlorine atom under milder conditions.

Replacement of $Cl$ of chlorobenzene to give phenol requires drastic conditions,but chlorine of $2,4-$dinitrochlorobenzene is readily replaced because:

Similar Questions

Which of the following groups acts as both $-I$ effect and $o, p$-directing group?

Which of the following reactions is a Fittig reaction?

The product $(A)$ in the following reaction is:

What is $A$ in the following reaction?
Benzyl chloride + $Cl_2 \xrightarrow{FeCl_3} A + \text{p-chlorobenzyl chloride}$

The rate of reaction is maximum if $G$ is:

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