Step 1: Test each reagent against the known reactions of glucose.
Step 2: Bromine water oxidises the \( -CHO \) group of glucose to gluconic acid, so a reaction occurs.
Step 3: Phenylhydrazine \( (C_6H_5NHNH_2) \) reacts with glucose to give the yellow crystalline osazone, so a reaction occurs.
Step 4: Acetic anhydride \( (CH_3CO)_2O \) acetylates the five \( -OH \) groups to give glucose pentaacetate, so a reaction occurs.
Step 5: Glucose does NOT form the aldehyde-bisulphite addition product with \( NaHSO_3 \). This failure shows that the free \( -CHO \) group is largely absent because glucose exists mainly as a cyclic hemiacetal.
Answer: \( NaHSO_3 \).