Published by Patrick Mutisya · 14 days ago
State that glucose, fructose and maltose are reducing sugars and that sucrose is a non‑reducing sugar.
A reducing sugar is any carbohydrate that possesses a free carbonyl group (an aldehyde or a ketone) capable of acting as a reducing agent. In aqueous solution the carbonyl group can be oxidised, while the sugar itself reduces metal ions such as Cu²⁺ in Benedict’s or Fehling’s reagents.
In the open‑chain form a monosaccharide contains a carbonyl group:
\$\text{R–C(=O)–H} \quad \text{(aldehyde)}\$
or
\$\text{R–C(=O)–R'} \quad \text{(ketone)}\$
If this carbonyl carbon is not involved in a glycosidic bond, the sugar can act as a reducing agent. When the carbonyl carbon participates in a glycosidic linkage, the reducing ability is blocked, giving a non‑reducing sugar.
| Sugar | Type | Reducing Ability | Key Test Result |
|---|---|---|---|
| Glucose | Monosaccharide (aldose) | Reducing | Positive (brick‑red precipitate) |
| Fructose | Monosaccharide (ketose) | Reducing | Positive (after isomerisation to aldehyde form) |
| Maltose | Disaccharide (α‑1,4‑linked glucose) | Reducing | Positive |
| Sucrose | Disaccharide (glucose‑fructose) | Non‑reducing | Negative |
In sucrose the glycosidic bond joins the anomeric carbon of glucose (C1) to the anomeric carbon of fructose (C2). Both carbonyl carbons are therefore involved in the bond, eliminating any free aldehyde or ketone group. Consequently sucrose cannot reduce Cu²⁺ ions and gives a negative result in Benedict’s or Fehling’s tests.