Step 1: Understanding optical isomerism. Optical isomerism arises when a compound has a chiral center (an atom, usually carbon, attached to four different groups). Lactic acid (\( \text{CH}_3\text{CH}(\text{OH})\text{COOH} \)) contains one chiral carbon atom, making it capable of existing as two enantiomers (non-superimposable mirror images).
Step 2: Calculation of optical isomers. The number of optical isomers for a compound is given by \( 2^n \), where \( n \) is the number of chiral centers. For lactic acid, \( n = 1 \): \[ \text{Number of optical isomers} = 2^1 = 2 \]
Step 3: Why other options are incorrect. - (A) 4: This would require two chiral centers.
- (B) 0: Incorrect, as lactic acid has a chiral center.
- (C) 6: This is not possible with one chiral center.

Consider the following molecule (X).
The Structure X is? 
How many different stereoisomers are possible for the given molecule? 
Match the following:
(P) Schedule H
(Q) Schedule G
(R) Schedule P
(S) Schedule F2
Descriptions:
(I) Life period of drugs
(II) Drugs used under RMP
(III) List of Prescription Drugs
(IV) Standards for surgical dressing
Choose the correct match of laxative and its Mechanism of Action (MOA):
