Which one of the following would undergo hydrolysis most readily with aqueous sodium hydroxide to form the corresponding hydroxy derivatives?

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Solution

The correct option is A

Electron withdrawing groups like – $N O_{2}$ at ortho and para positions makes aryl halides more reactive towards nucleophilic substitution reactions

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Which one of the following would undergo hydrolysis most readily with aqueous sodium hydroxide to form the corresponding hydroxy derivatives?

The correct option is A Electron withdrawing groups like – NO2 at ortho and para positions makes aryl halides more reactive towards nucleophilic substitution reactions

The correct option is A

Electron withdrawing groups like – $N O_{2}$ at ortho and para positions makes aryl halides more reactive towards nucleophilic substitution reactions