Addition of KI accelerates the hydrolysis of | vedclass

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(D) The addition of $KI$ accelerates the hydrolysis of primary alkyl halides because the iodide ion $(I^-)$ acts as a powerful nucleophile,which attac

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the iodide ion is a powerful nucleophile as well as a good leaving group

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(D) The addition of $KI$ accelerates the hydrolysis of primary alkyl halides because the iodide ion $(I^-)$ acts as a powerful nucleophile,which attacks the alkyl halide to form a more reactive alkyl iodide intermediate $(R-I)$.Since $I^-$ is also a very good leaving group,it facilitates the subsequent substitution reaction with water or hydroxide ions,thereby increasing the overall rate of hydrolysis.

Addition of $KI$ accelerates the hydrolysis of primary alkyl halides because

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