Which of the following compounds has difficul | vedclass

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(C) The reactivity of haloarenes towards nucleophilic substitution increases with the presence of electron-withdrawing groups (like $-NO_2$) at the $o

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$m-$Nitrochlorobenzene

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(C) The reactivity of haloarenes towards nucleophilic substitution increases with the presence of electron-withdrawing groups (like $-NO_2$) at the $ortho$ and $para$ positions due to the stabilization of the carbanion intermediate.Electron-withdrawing groups at the $meta$ position have a negligible effect on the reactivity compared to $ortho$ and $para$ positions.Therefore,among the given options,$m-$nitrochlorobenzene is the least reactive,making it the most difficult to break the $C-X$ bond during a nucleophilic substitution reaction.

Which of the following compounds has difficulty in breaking the $C-X$ bond during a nucleophilic substitution reaction?

Similar Questions

The $C-Cl$ bond lengths (in $pm$) in haloarene and haloalkane are respectively:

In the reaction shown below,the $o/p$ ratio will be highest when:
$C_6H_5R + HNO_3 \xrightarrow{H_2SO_4} o-\text{nitro-substituted product} + p-\text{nitro-substituted product}$

For the given reaction,identify the major product $C$.

Chlorobenzene reacts with trichloroacetaldehyde (chloral) in the presence of $H_2SO_4$.
$2 C_6H_5Cl + CCl_3CHO \xrightarrow{H_2SO_4} \text{Major Product}$
The major product formed is:

In which reaction does nitrobenzene give $o$- and $p$-substituted products?

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