The correct structure of the dipeptide gly-al | vedclass

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(C) dipeptide is formed by the condensation of two amino acids, where the carboxyl group $(-COOH)$ of one amino acid reacts with the amino group $(-NH

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(C) dipeptide is formed by the condensation of two amino acids, where the carboxyl group $(-COOH)$ of one amino acid reacts with the amino group $(-NH_2)$ of another to form a peptide bond $(-CO-NH-)$.For the dipeptide gly-ala (Glycine-Alanine):$1$. Glycine $(NH_2-CH_2-COOH)$ is the $N$-terminal amino acid.$2$. Alanine $(NH_2-CH(CH_3)-COOH)$ is the $C$-terminal amino acid.$3$. The peptide bond is formed between the $-COOH$ of Glycine and the $-NH_2$ of Alanine.$4$. The resulting structure is $NH_2-CH_2-CO-NH-CH(CH_3)-COOH$.

The correct structure of the dipeptide gly-ala is

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