

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.
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.
For $ \alpha, \beta, \gamma \in \mathbb{R} $, if $$ \lim_{x \to 0} \frac{x^2 \sin \alpha x + (\gamma - 1)e^{x^2} - 3}{\sin 2x - \beta x} = 3, $$ then $ \beta + \gamma - \alpha $ is equal to: