Question:

Sucrose is dextrorotatory but after hydrolysis the mixture show laevorotation, this is because of

Updated On: Apr 10, 2025
  • Laevorotation of glucose is more than dextrorotation of fructose.
  • Sucrose is a non-reducing sugar.
  • Recemic mixture is formed.
  • Laevorotation of fructose is more than dextrorotation of glucose.
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The Correct Option is D

Approach Solution - 1

Sucrose is a disaccharide consisting of glucose and fructose. Sucrose itself is dextrorotatory, meaning it rotates plane-polarized light to the right. However, when sucrose undergoes hydrolysis, it breaks down into glucose and fructose. The resulting mixture shows laevorotation (rotation to the left). This occurs because of the individual optical activities of glucose and fructose.

Explanation: 

The key reason the mixture shows laevorotation after hydrolysis is that fructose is more laevorotatory than glucose is dextrorotatory. Thus, after hydrolysis, the laevorotation of fructose outweighs the dextrorotation of glucose, leading to an overall laevorotatory mixture.

Review of the options:

  • Option A: "Racemization is formed" - This is incorrect. The reaction does not form a racemic mixture, but rather a mixture of fructose and glucose.
  • Option B: "Laevorotation of fructose is more than dextrorotation of glucose" - This is the correct answer. Fructose has a greater laevorotatory effect than glucose's dextrorotatory effect, which causes the overall mixture to exhibit laevorotation after hydrolysis.
  • Option C: "Laevorotation of glucose is more than dextrorotation of fructose" - This is incorrect. Glucose does not exhibit stronger laevorotation than fructose.
  • Option D: "Sucrose is a non-reducing sugar" - While sucrose is indeed a non-reducing sugar, this fact does not explain the optical rotation observed after hydrolysis.

Conclusion:

The correct answer is Option B: Laevorotation of fructose is more than dextrorotation of glucose.

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Approach Solution -2

Sucrose is dextrorotatory, but after hydrolysis, the mixture shows laevorotation. This is because of: 

(A) Laevorotation of glucose is more than dextrorotation of fructose. 
(B) Sucrose is a non-reducing sugar. 
(C) A racemic mixture is formed. 
(D) Laevorotation of fructose is more than dextrorotation of glucose. 

The correct answer is (D): Laevorotation of fructose is more than dextrorotation of glucose. 

\(\textbf{Explanation:}\) Sucrose is a disaccharide composed of glucose and fructose. While sucrose itself is dextrorotatory, the hydrolysis of sucrose breaks it down into glucose and fructose. Glucose is dextrorotatory, while fructose is laevorotatory. After hydrolysis, the resultant mixture shows a net laevorotation because fructose has a higher laevorotatory effect than the dextrorotatory effect of glucose.

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