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Multiple Choice
Provide the generic name, including stereochemistry, for the following monosaccharide:
A
L-aldotetrose
B
D-aldotetrose
C
L-aldopentose
D
D-ketopentose
Verified step by step guidance
1
Identify the functional groups present in the structure. The molecule has an aldehyde group (CHO) at the top, indicating it is an aldose.
Count the number of carbon atoms in the main chain. There are four carbon atoms, which classifies the sugar as a tetrose.
Determine the configuration of the chiral centers. The hydroxyl group on the second carbon from the bottom is on the left, indicating an L-configuration.
Combine the information: Since it is an L-configuration, has an aldehyde group, and contains four carbon atoms, the sugar is an L-aldotetrose.
Review the options provided: L-aldotetrose, D-aldotetrose, L-aldopentose, D-ketopentose. The correct classification based on the analysis is L-aldotetrose.