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.
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? 
How many different stereoisomers are possible for the given molecule? 

A current-carrying coil is placed in an external uniform magnetic field. The coil is free to turn in the magnetic field. What is the net force acting on the coil? Obtain the orientation of the coil in stable equilibrium. Show that in this orientation the flux of the total field (field produced by the loop + external field) through the coil is maximum.