Nucleophilic reaction reactivity order

Started by Pranjal Singh, May 22, 2021, 04:12:49 AM

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Pranjal Singh

Here it is
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uma

Answer C is right
Methanol is a weak nucleophile and hence mechanism favored is SN1
Iodine (best leaving group) and tertiary benzylic  (I) will show fastest reaction  due to stability of carbocation and with  bromobenzene  (III) will show no reaction because phenyl carbocations are least stable.

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