Major product of the following reaction is

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(D) The reaction proceeds in two steps: $1$. Nucleophilic substitution: The amino group of glycinamide attacks the acid chloride to form an amide link

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(D) The reaction proceeds in two steps: $1$. Nucleophilic substitution: The amino group of glycinamide attacks the acid chloride to form an amide linkage,releasing $HCl$. Triethylamine $(Et_3N)$ is used to neutralize the $HCl$ produced. $2$. Free radical polymerization: The resulting monomer,which contains a vinyl group,undergoes free radical polymerization to form the final polymer product. The structure of the final polymer is shown in option $D$.

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