Chemistry, asked by harleyquinn24, 11 months ago

hydrolysis of benzyl chloride follows sN1 mechanism. justify this statement with the help of suitable mechanism.

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Answered by Anonymous

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Benzyl chloride will undergo Sn1 reaction faster as it will form stable 2° carbocation which can be stabilized by π electrons of benzene ring. Whereas in case of methyl chloride, 1° carbocation is formed which is least stable. ... Which is more reactive towards an SN2 reaction, methyl chloride or CH2=CH-Cl?

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