Question #86320
1 Answer
Sep 20, 2017
You get 3-methylpentan-3-ol as the product.
Explanation:
Grignard reagents convert esters to tertiary alcohols.
Thus, we predict the product to be 3-methylpentan-3-ol.
Here are the steps in the mechanism.
Step 1. Nucleophilic attack on the carbonyl group
Step 2. Loss of the methoxide ion
Step 3. A second nucleophilic attack by the Grignard Reagent
Step 4. Protonation of the alkoxide