Gly-Ala (Glycylalanine) is a dipeptide composed of: - Glycine (Gly) as the N-terminal amino acid.
- Alanine (Ala) as the C-terminal amino acid. Correct structural features: - Free amino group (-NH$_2$) at the N-terminus.
- Free carboxyl group (-COOH) at the C-terminus.
- Peptide bond (-CO-NH-) linking the two amino acids.
- Methyl side chain (-CH$_3$) from alanine. Analysis of options: - Option 1: Shows two separate amino acids (Gly + Ala), not a dipeptide.
- Option 2: Correct dipeptide structure with proper peptide bond.
- Option 3: Incorrect hydroxyl group (OH) at N-terminus.
- Option 4: Shows ester linkage (-CO-O-) instead of peptide bond.
Thus, the correct answer is (2).
Glycylalanine is a dipeptide formed from two amino acids:
When these two amino acids undergo a condensation reaction, the carboxyl group of glycine reacts with the amino group of alanine, releasing a water molecule and forming a peptide bond (–CO–NH–).
Resulting Dipeptide Structure (Gly-Ala):
H2N–CH2–CO–NH–CH(CH3)–COOH
The image shown above correctly represents the structure of Glycylalanine, featuring:
Final Answer:
The given structure is Gly-Ala (Glycylalanine)
Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
(a) Define the following:
(i) Enantiomers
(ii) Racemic mixture
The CORRECT statement(s) regarding the given molecules is(are):