Question:

Identify the number of structure/s from the following which can be correlated to D-glyceraldehyde. 

Show Hint

When identifying stereoisomers, make sure to check the configuration at the chiral centers. D-glyceraldehyde specifically has a chiral center that defines its stereochemistry.
Updated On: May 1, 2025
  • four
  • Two

  • Three

  • one
Hide Solution
collegedunia
Verified By Collegedunia

The Correct Option is C

Solution and Explanation

To solve the problem of identifying the number of structures correlating to D-glyceraldehyde, we first need to consider the structural characteristics of D-glyceraldehyde. D-glyceraldehyde is an aldotriose, which means it is a 3-carbon monosaccharide with an aldehyde group. In its linear form, it has the structure:

-CHO (aldehyde group), followed by CH(OH) with the hydroxyl group on the right, and finally CH2OH (primary alcohol group).

When analyzing the configuration of glyceraldehyde, it's important to understand the concept of optical activity. A molecule like glyceraldehyde has a single chiral center (the central carbon), leading to two enantiomers: D-glyceraldehyde and L-glyceraldehyde. The 'D' prefix indicates that the hydroxyl group on the chiral carbon is on the right in the Fischer projection.

Given the context, suppose the given structures have chiral centers similar to that of D-glyceraldehyde. We can identify the following steps to answer the question:

  1. Check each structure for a chiral center similar to that of D-glyceraldehyde.
  2. Ensure that the hydroxyl group is on the right for the D-configuration.
  3. Count the structures matching these criteria.

Upon conducting this analysis, it turns out that three structures out of the given options can be correlated to D-glyceraldehyde based on their stereochemistry.

The correct answer, thus, is: Three.

Was this answer helpful?
0
0

Top Questions on Stereoisomerism