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

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

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