
Optical activity refers to molecules that have a chiral center (at least one) and have a non-superimposable mirror image.
For example, consider the molecule shown below:
$$ \text{CH}_3\text{-CH}_2\text{-C}^*\text{-CH}_3 $$
(Chiral center - optically active)
The chiral center is the carbon atom bonded to four different substituents, which makes it optically active. This means that the molecule can rotate plane-polarized light.

A compound is optically active if it has at least one chiral center (a carbon atom attached to four different groups). Let us analyze the given compounds:
CH$_3$-CH(OH)-CH(OH)-CH$_3$: This compound has two hydroxyl groups (OH) on adjacent carbon atoms. Both hydroxyl groups are equivalent, and the molecule has a plane of symmetry, making it optically inactive.
CH$_3$-CH$_2$-CH$_2$-OH: This compound has no chiral centers, as all carbons are attached to at least two identical groups. Therefore, it is optically inactive.
CH$_3$-CH$_2$-CH-CH$_3$ (with a Cl on the second carbon):} The second carbon atom is a chiral center, as it is attached to four different groups: CH$_3$, H, Cl, and CH$_2$CH$_3$. Hence, this compound is optically active.
(CH$_3$)$_2$CH-CH$_2$-CH$_2$-Cl: The molecule does not have any chiral centers, as the carbon bonded to the chlorine atom is not attached to four different groups. Therefore, it is optically inactive.
Conclusion: Among the given compounds, only CH$_3$-CH$_2$-CH-CH$_3$ (with Cl on the second carbon) is optically active.

Consider the following molecule (X).
The Structure X is? 
How many different stereoisomers are possible for the given molecule? 
Consider the following sequence of reactions : 
Molar mass of the product formed (A) is ______ g mol\(^{-1}\).

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: