Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
Assertion (A) is false, but Reason (R) is true.
Step 1: Understanding optical activity of amino acids. All naturally occurring \(\alpha\)-amino acids, except for glycine, are optically active because they contain a chiral carbon atom (except glycine, which has two hydrogen atoms on the chiral center, making it achiral).
Step 2: L-configuration of amino acids. Most naturally occurring amino acids are in the L-configuration, which is why they are optically active (except glycine).
Step 3: Conclusion. Thus, both Assertion (A) and Reason (R) are true, and Reason (R) correctly explains Assertion (A), making option (A) the correct answer.
Consider the following molecule (X).
The Structure X is?
(a) Define the following:
(i) Enantiomers
(ii) Racemic mixture
The CORRECT statement(s) regarding the given molecules is(are):
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