Given Compound (Y):
The structure of compound Y is as follows:
\( \text{Br} - [\text{:: 60}] - [\text{:: -60}] \text{H} - [\text{:: -60}] - [\text{:: -60}] (\text{CH}_3) - [\text{:: -60}] \text{H} \)
In this compound:
To identify the enantiomer of Y, we need to find structures that are mirror images of Y but non-superimposable.
Analysis of the Options:
Conclusion: Both (B) and (C) are enantiomers of Y. Therefore, the correct answer is: (B), (C).
How many different stereoisomers are possible for the given molecule?
Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.