Question
Question: The major product in the following reaction is:  to Mg (II). The reaction is therefore known as an oxidative insertion or oxidative addition.
In this reaction, in the first step, the nucleophilic methyl group will attack on the electrophilic end of the carbonyl centre. Due to which a negative charge is generated on oxygen atom then in the second step there is a bimolecular substitution reaction on carbon containing chloride and chloride is removed. And overall, there is a formation of five membered compounds.
**Hence, option (D) is the correct option.
Note: **
Grignard reagents easily remove acidic protons. These strong nucleophilic reagents like Grignard reagents and organolithiums are strong bases, and may need protection from acidic protons as well as from electrophilic carbonyl groups. Among the most troublesome are the protons of hydroxyl groups.