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Question 109 of 110

Q.Define the following terms:

(i) Oligosaccharides
(ii) Invert sugar
Telangana TsbieCBSE Class XII Board 2020Subjective· 2mImportance★★★★★
99% · 109/110 Questions
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Oligosaccharides are carbohydrates composed of 2–10 monosaccharide units linked by glycosidic bonds; invert sugar is an equimolar mixture of glucose and fructose obtained by hydrolyzing sucrose, named for its ability to rotate plane-polarized light in the opposite direction.

The Concept Behind These Terms

Both terms belong to carbohydrate chemistry, a core topic in biomolecules for Indian exams (NEET, JEE, Class 12 boards). The key idea is that carbohydrates are classified by their degree of polymerization — how many simple sugar units are linked together. Oligosaccharides sit between monosaccharides (single units) and polysaccharides (many units). Invert sugar is a special case: it’s not a single molecule but a mixture formed when a disaccharide (sucrose) is broken down, and its name comes from a striking optical property change.

Let’s define each term clearly, with the reasoning that matters for exams.


(i) Oligosaccharides

1. What the name means

The prefix “oligo-” comes from Greek, meaning “few” or “small.” So oligosaccharides are carbohydrates made of a small number of monosaccharide units — typically 2 to 10 — joined together by glycosidic bonds.

2. The classification rule

In standard biochemistry, carbohydrates are grouped as:

  • Monosaccharides: 1 unit (e.g., glucose, fructose)
  • Oligosaccharides: 2–10 units
  • Polysaccharides: more than 10 units (often hundreds or thousands)
Note

For exam purposes, the most common oligosaccharides are disaccharides (2 units), like sucrose, maltose, and lactose. Trisaccharides (3 units) like raffinose are also oligosaccharides but appear less frequently in board questions.

3. How they are formed

Monosaccharides link through a glycosidic bond — a covalent bond formed between the anomeric carbon of one sugar and a hydroxyl group of another, with the elimination of a water molecule (condensation reaction). For example, in sucrose, glucose and fructose are linked by an α\alpha‑1,2‑glycosidic bond.

4. Key properties to remember

  • They can be reducing or non-reducing depending on whether a free anomeric carbon is available. Sucrose is non-reducing; maltose and lactose are reducing.
  • They are sweet-tasting and water-soluble.
  • They can be hydrolyzed into their constituent monosaccharides by acids or specific enzymes.
Watch out

A common mistake: thinking “oligosaccharide” means only disaccharides. It includes any carbohydrate with 2–10 units — so a trisaccharide is also an oligosaccharide. But for most exam questions, you’ll deal with disaccharides.

Final definition for (i):

Oligosaccharides are carbohydrates that yield 2 to 10 monosaccharide units upon hydrolysis, linked by glycosidic bonds.


(ii) Invert Sugar

1. Where it comes from

Invert sugar is not a naturally occurring single compound — it is a mixture produced by the hydrolysis of sucrose (common table sugar). Sucrose is a disaccharide of glucose and fructose.

2. The hydrolysis reaction

C12H22O11+H2O→dilute acid or enzyme invertaseC6H12O6(glucose)+C6H12O6(fructose)\text{C}_{12}\text{H}_{22}\text{O}_{11} + \text{H}_2\text{O} \xrightarrow{\text{dilute acid or enzyme invertase}} \text{C}_6\text{H}_{12}\text{O}_6 (\text{glucose}) + \text{C}_6\text{H}_{12}\text{O}_6 (\text{fructose})

The product is an equimolar mixture of D‑glucose and D‑fructose.

3. Why “invert”? The optical rotation story

This is the fascinating part — and a favourite exam point. Sucrose is dextrorotatory (rotates plane-polarized light to the right, [α]D=+66.5∘[\alpha]_D = +66.5^\circ). When hydrolyzed:

  • Glucose is also dextrorotatory ([α]D=+52.5∘[\alpha]_D = +52.5^\circ).
  • Fructose is strongly laevorotatory (rotates light to the left, [α]D=−92∘[\alpha]_D = -92^\circ). …

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