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(A) The reaction of a Grignard reagent $(R-MgX)$ with a ketone $(R'-CO-R'')$ follows a nucleophilic addition mechanism. $1$. The nucleophilic alkyl gr

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Tertiary alcohol

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(A) The reaction of a Grignard reagent $(R-MgX)$ with a ketone $(R'-CO-R'')$ follows a nucleophilic addition mechanism. $1$. The nucleophilic alkyl group $(R^-)$ from the Grignard reagent attacks the electrophilic carbonyl carbon of the ketone. $2$. This forms an alkoxide intermediate $(R'-C(R)(O^-MgX^+)-R'')$. $3$. Subsequent acidic hydrolysis of this intermediate yields a tertiary alcohol $(R'-C(OH)(R)-R'')$. Therefore,the reaction of a Grignard reagent with a ketone produces a tertiary alcohol.

What product is obtained from the reaction of a Grignard reagent with a ketone?

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