The reactant 'A' in the below-mentioned reaction is:
 

1.	Benzoyl chloride	2.	Toluene
3.	Acetophenone	4.	Benzoic acid

An acid that forms an anhydride (X) on heating and an acid imide (Y) on strong heating with ammonia is:

1.		2.
3.		4.

The product 'X' in the below mentioned reaction is:

1.		2.
3.		4.

The reaction between benzaldehyde and acetophenone in the presence of dilute NaOH is known as:

1. Cannizzaro's reaction

2. Cross Cannizzaro's reaction

3. Cross aldol condensation

4. Aldol condensation

The product of the below-mentioned reaction is:

1.		2.
3.		4.

The self-condensation product of two moles of ethyl acetate in the presence of sodium ethoxide yield is: 

1. Ethyl butyrate

2. Acetoacetic ester

3. Methyl acetoacetate

4. Ethyl propionate

The nucleophilic addition reaction will be most favored among the given compounds is:

1. $C{H}_{3}C{H}_{2}C{H}_{2}COC{H}_3$

2. $(C{H}_3{)}_{2}C=O$

3. $C{H}_{3}C{H}_{2}CHO$

4. $C{H}_{3}CHO$

A carbonyl compound reacts with hydrogen cyanide to form cyanohydrins, which form a racemic mixture of α-hydroxy acid on hydrolysis. The carbonyl compound is:

1. Acetaldehyde

2. Acetone

3. Diethyl ketone

4. Formaldehyde

A compound with the molecular formula C₅H₁₀ that yields acetone on ozonolysis is:
1. 2-Methyl-2-butene
2. 2-Methyl-1-butene
3. Cyclopentane
4. 3-Methyl-1-butene

Reduction of aldehydes and ketones into hydrocarbons using amalgam and conc. HCl is called:

1. Clemmensen reduction

2. Cope reduction

3. Dow reduction

4. Wolff-Kishner reduction