Step 1: Understanding the Concept:
$\alpha$-D-glucose and $\beta$-D-glucose are cyclic diastereomers of glucose that differ in configuration only at the hemiacetal carbon (C-1).
These cyclic isomers are called anomers.
Detailed Explanation:
- Evaluating Assertion (A): Pure, freshly prepared crystalline $\alpha$-D-glucose and $\beta$-D-glucose possess distinct physical and optical properties.
Specifically, a freshly prepared solution of pure $\alpha$-D-glucose has a specific optical rotation of $+112.2^\circ$, while a freshly prepared solution of pure $\beta$-D-glucose has a specific optical rotation of $+18.7^\circ$.
Therefore, their initial optical properties are not identical, making Assertion (A) false.
- Evaluating Reason (R): When dissolved in water, both anomers undergo an interconversion process called mutarotation.
The ring opens to form the straight-chain intermediate and then closes to form either the $\alpha$ or $\beta$ anomer.
Over time, both solutions reach the exact same thermodynamic equilibrium.
This equilibrium mixture consists of approximately $36\%$ $\alpha$-D-glucose, $64\%$ $\beta$-D-glucose, and trace amounts ($<0.1\%$) of the open-chain form, resulting in a stable specific rotation of $+52.7^\circ$.
Thus, both solutions eventually form the identical equilibrium mixture, making Reason (R) true.
Step 2: Final Answer:
Assertion (A) is false but Reason (R) is true. This corresponds to option (D).