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,
Answer:
And what is your question
Explanation: