Show how you would use the malonic ester synthesis to make the following compounds

Step1: Malonic ester synthesis

It’s a method in which a substituted derivative of acetic acid is formation occur in the presence of sodium ethoxide from dimethyl malonate followed by alkylation or acylation then hydrolysis followed by decarboxylation to form a derivate of acetic acid as a product.

Ethoxide is used as a base to form an enolate ion which on further reaction with the alkyl halide the alkylation that occur means the removal of the halide ion the alkyl group attached at the alpha position to the carbonyl.

It is the reaction that lead to the removal of the carbonyl group and releases carbon dioxide$\left({\mathrm{CO}}_2\right)$. Decarboxylation occurs by providing heat in the reaction.

1. Acidic hydrogen protonated
2. Formation of enolate ion
3. Alkylation
4. Decarboxylation
5. Derivative of acetic acid formed

Mechanism