MCQEasyJEE 2026Carbohydrates (Glucose, Fructose, Sucrose…)

JEE Chemistry 2026 Question with Solution

Structures of four disaccharides are given below. Among the given disaccharides, the non-reducing sugar is:

Four numbered disaccharide structures are shown, each with two monosaccharide rings linked by a glycosidic oxygen bond and multiple OH labels, asking to identify the non-reducing sugar among structures 1 to 4.
  • A

    Maltose

  • B

    Lactose

  • C

    Sucrose

  • D

    Cellobiose

Answer

Correct answer:C

Step-by-step solution

Standard Method

Given: Structures of four disaccharides are given and we have to identify the non-reducing sugar.

Find: Which among maltose, lactose, sucrose, and cellobiose is non-reducing.

Concept: Reducing sugars have a free anomeric carbon atom with a free OH-OH group on the hemiacetal carbon, so they can open to form an aldehyde or ketone group. Non-reducing sugars do not have a free anomeric carbon because both anomeric carbons are involved in glycosidic linkage.

Step 1: Analyze each disaccharide.

  • Maltose: formed from two glucose units with α(14)\alpha(1 \to 4) linkage. One anomeric carbon is free, so it is a reducing sugar.
  • Lactose: formed from glucose and galactose with β(14)\beta(1 \to 4) linkage. One anomeric carbon is free, so it is a reducing sugar.
  • Sucrose: formed from glucose and fructose with α(12)\alpha(1 \to 2) and β(21)\beta(2 \to 1) linkage. Both anomeric carbons are involved in the glycosidic bond, so it is non-reducing.
  • Cellobiose: formed from two glucose units with β(14)\beta(1 \to 4) linkage. One anomeric carbon is free, so it is a reducing sugar.

Step 2: Conclusion. Sucrose is the only non-reducing sugar among the given disaccharides.

Therefore, the correct option is C.

Anomeric Carbon Check

Given: A set of disaccharides is provided.

Find: The non-reducing sugar.

A quick test is to check whether both anomeric carbons are tied up in the glycosidic bond. If both are involved, the sugar is non-reducing. If at least one anomeric carbon remains free, the sugar is reducing.

Among the listed sugars, only sucrose has both anomeric carbons involved in bond formation.

Therefore, the correct option is C.

Common mistakes

  • Mistake: Treating every disaccharide as non-reducing. Why it is wrong: a disaccharide is non-reducing only when both anomeric carbons are involved in the glycosidic bond. What to do instead: check whether any anomeric carbon remains free.

  • Mistake: Looking only at the presence of a glycosidic linkage and ignoring which carbon atoms are connected. Why it is wrong: the reducing character depends specifically on the anomeric carbons, not merely on bond formation. What to do instead: identify the anomeric carbon in each monosaccharide unit first.

  • Mistake: Confusing α\alpha or β\beta linkage with reducing or non-reducing nature. Why it is wrong: α\alpha and β\beta describe stereochemistry, not whether a free anomeric carbon is present. What to do instead: determine reducing nature by checking for a free hemiacetal carbon.

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