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).
Which of the following is true for the stereochemical relationship of the given structures (A-D)?
Consider the following molecule (X).
The Structure X is?
Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
A quantity \( X \) is given by: \[ X = \frac{\epsilon_0 L \Delta V}{\Delta t} \] where:
- \( \epsilon_0 \) is the permittivity of free space,
- \( L \) is the length,
- \( \Delta V \) is the potential difference,
- \( \Delta t \) is the time interval.
The dimension of \( X \) is the same as that of: