What is the product formed when a Grignard re | vedclass

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(A) The reaction of a $Grignard$ reagent $(RMgX)$ with a ketone like acetone $(CH_3COCH_3)$ proceeds via nucleophilic addition to the carbonyl group.

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Tertiary alcohol

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(A) The reaction of a $Grignard$ reagent $(RMgX)$ with a ketone like acetone $(CH_3COCH_3)$ proceeds via nucleophilic addition to the carbonyl group. The nucleophilic alkyl group $(R^-)$ from the $Grignard$ reagent attacks the electrophilic carbonyl carbon of the acetone. This forms an intermediate magnesium alkoxide: $CH_3-C(R)(OMgX)-CH_3$. Upon acidic hydrolysis $(H_3O^+)$,this intermediate is converted into a tertiary alcohol with the structure $CH_3-C(R)(OH)-CH_3$.

What is the product formed when a $Grignard$ reagent $(RMgX)$ reacts with acetone $(CH_3COCH_3)$?

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