why is methyl chloride hydrolysed more easily than chlorobenzene

Dear student!
Actually, the lone pair of chlorine atom is delocalised over the conjugated double bond ring of benzene which adds a double bond character to the C-Cl bond of the chlorobenzene which makes the bond shorter and stronger too, so the hydrolysis becomes difficult while in alkyl halides i.e. methyl chloride there is a single bond and polarity too which is easily hydrolyzed.

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becoz in hydrolising Cl-benzene intermediate loses aromatisity which is unstable

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