The given ketone when reacted with base gave enolate, the enolate formed due to loss of methylene proton next to carbonyl group. Enolate when treated with methyle Bromide gave alpha substituted product.
Strong absorption around 1713 cm⁻¹ in IR spectrum confirms the presence of Carbonyl group.
The product along with ¹H-NMR values is given below,
Strong absorption around 1713 cm⁻¹ in IR spectrum confirms the presence of Carbonyl group.
The product along with ¹H-NMR values is given below,