Carboxylic acids have higher boiling points than aldehydes, ketones and even alcohols of comparable molecular mass. It is due to:

1.	Formation of intramolecular H-bonding
2.	Formation of carboxylate ion
3.	More extensive association of carboxylic acid via van der waals force of attraction
4.	Formation of intermolecular H-bonding

In the below reaction, the structure of "A" is:

1.		2.
3.		4.

What is the correct order of the carboxylic acids' strength?

I.

II.

III.

The correct statement regarding a carbonyl compound with a hydrogen atom on its alpha-carbon is:

The product formed by the reaction of an aldehyde with a primary amine is:
1. Ketone
2. Carboxylic acid
3. Aromatic acid
4. Schiff base

The esters that get hydrolyzed most easily under alkaline conditions is?

1.
2.
3.
4.

The reaction of a carbonyl compound with one of the following reagents involves nucleophilic addition followed by the elimination of water. The reagents are:

Compounds that can exhibit tautomerism, are:

1. l and ll
2. l and lll
3. ll and lll
4. l, ll and lll