Question:

Which of the following represents α-D-fructofuranose?

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In α-D-fructofuranose, the hydroxyl group at the anomeric carbon is in the axial position, which distinguishes it from the β-anomer, where it is in the equatorial position.
Updated On: May 14, 2025
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The Correct Option is A

Solution and Explanation

- α-D-fructofuranose is the six-membered cyclic form of D-fructose, a monosaccharide. It forms a furanose ring structure and the hydroxyl group at the anomeric carbon (C1) is in the axial position, which makes it α-D-fructofuranose.
- In the options, the structure in (1) is the correct representation of α-D-fructofuranose, showing the furanose ring and the correct orientation of the hydroxyl group at the anomeric carbon.
Thus, the correct answer is (1).
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