The compound from which chlorobenzene cannot | vedclass

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(C) Step $1$: Chlorobenzene can be prepared from aniline via the Sandmeyer reaction using $NaNO_2/HCl$ followed by $CuCl/HCl$.Step $2$: It can be prep

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Phenol

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(C) Step $1$: Chlorobenzene can be prepared from aniline via the Sandmeyer reaction using $NaNO_2/HCl$ followed by $CuCl/HCl$.Step $2$: It can be prepared from benzene via electrophilic substitution using $Cl_2/FeCl_3$.Step $3$: It can be prepared from benzene diazonium chloride via the Sandmeyer reaction.Step $4$: In phenol, the $C-O$ bond has partial double bond character due to resonance, making it very strong and difficult to break to replace the $-OH$ group with a $-Cl$ atom. Thus, chlorobenzene is not easily prepared from phenol.

The compound from which chlorobenzene cannot be prepared easily is

Similar Questions

In Gattermann reaction,a diazonium group is replaced by $\underline{X}$ using $\underline{Y}$. $\underline{X}$ and $\underline{Y}$ are:
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