Glucose, a reducing sugar, can undergo various reactions due to its aldehyde group (in the open-chain form) and hydroxyl groups. Let’s analyze the options:
1. Conc. HNO₃ (Concentrated Nitric Acid): Glucose reacts with concentrated nitric acid to give glucaric acid (a sugar acid) through oxidation. Hence, glucose reacts with concentrated HNO₃.
2. Acetic Anhydride: Glucose reacts with acetic anhydride to form acetates (esters) by esterification of the hydroxyl groups.
Therefore, glucose reacts with acetic anhydride.
3. Hydroxylamine: Hydroxylamine reacts with aldehydes, such as the aldehyde group in glucose, to form oximes.
Therefore, glucose reacts with hydroxylamine.
4. Sodium bisulphite: Sodium bisulphite reacts with aldehydes to form adducts, but glucose does not react with sodium bisulphite in the same manner as aldehydes or ketones. Glucose’s aldehyde group in the open-chain form is not easily reactive with sodium bisulphite compared to other aldehydes.
Thus, the correct answer is Sodium bisulphite.