Question:

Assertion (A): Sucrose is a non-reducing sugar and does not exhibit mutarotation.
Reason (R): In sucrose, both anomeric carbon atoms are involved in glycosidic bond formation.

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A sugar is non-reducing when all its anomeric carbon atoms are locked in glycosidic bond formation.
Updated On: Jun 8, 2026
  • Both Assertion and Reason are true, and Reason is the correct explanation of Assertion.
  • Both Assertion and Reason are true, but Reason is not the correct explanation of Assertion.
  • Assertion is true, but Reason is false.
  • Assertion is false, but Reason is true.
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The Correct Option is A

Solution and Explanation

Concept: Reducing sugars possess a free anomeric carbon capable of opening into the aldehydic or ketonic form. Mutarotation also requires the presence of a free hemiacetal or hemiketal carbon.

Step 1:
Structure of sucrose. Sucrose consists of: \[ \alpha\text{-D-glucose} \] and \[ \beta\text{-D-fructose} \] linked together.

Step 2:
Nature of glycosidic linkage. The linkage involves: \[ C_1 \text{ of glucose} \] and \[ C_2 \text{ of fructose} \] which are the anomeric carbon atoms.

Step 3:
Reducing property. Since both anomeric carbons participate in bond formation, neither unit can open into a free carbonyl form. Therefore sucrose is non-reducing.

Step 4:
Mutarotation. Mutarotation requires interconversion between \(\alpha\) and \(\beta\) forms through the open-chain structure. Because sucrose lacks a free anomeric carbon, mutarotation is not observed.

Step 5:
Both Assertion and Reason are correct, and the Reason properly explains the Assertion. \[ \boxed{\text{Option A}} \]
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