Biomolecules

14.3 

D-glucose reacts with hydroxylamine (NH₂OH) to form oxime due to the presence of the aldehyde functional group (-CHO). This is due to the cyclic structure of glucose which forms an open chain structure in an aqueous medium, which then reacts to give an oxime.

But in case of pentaacetate of D-glucose, it does not form open chain structure in an aqueous medium so it does not react with NH₂OH.

14.2

Lactose is a disaccharide carbohydrate (made up of two monosaccharide units) composed of β-D-galactose and β-D-glucose units. Hydrolysis breaks the glycosidic bond converting sucrose into β-D- galactose and β-D-glucose.

NOTE: But however, this reaction is so slow that it takes years for the solution of sucrose to undergo negligible change. Hence an enzyme called sucrase is added to proceed rapidly.

14.1 

Glucose and sucrose are carbohydrates (optically active polyhydroxy aldehydes or ketones). 
Structure of glucose:

Structure of sucrose:

As you can see both the compounds have five –OH and eight –OH groups respectively. These –OH groups are responsible for the extensive hydrogen bonding with water. This –H bonding is responsible for the solubility of glucose and sucrose in water.

In case of cyclohexane or benzene (simple six-membered ring compounds), they do not contain any – OH groups. Hence, they cannot undergo –H bonding with water and are insoluble.