
D-glyceraldehyde is the simplest monosaccharide with one chiral center. It is a three-carbon aldose with the following structural formula: \[ \text{CHO-CHOH-CHOH} \] Among the given structures:
- Structure (A) represents D-glyceraldehyde itself, as it matches the formula and configuration of D-glyceraldehyde.
- Structure (B) is an isomer, and the configuration matches that of D-glyceraldehyde.
- Structures (C) and (D) do not correlate to D-glyceraldehyde because they do not maintain the correct stereochemistry at the chiral center.
Thus, only two of the given structures (A) and (B) can be correlated to D-glyceraldehyde.
Consider the following molecule (X).
The Structure X is? 
How many different stereoisomers are possible for the given molecule? 
Which of the following is true for the stereochemical relationship of the given structures (A-D)?



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: