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 'X' in the below mentioned reaction is:

1.		2.
3.		4.

The substance that evolves NH₃ on boiling with NaOH is:

(1) Ethylamine

(2) Aniline

(3) Acetamide

(4) Acetoxime

Which of the following enzymes can hydrolyse urea into CO₂ and NH₃: 

1. Amylase

2. Urease

3. Lipase

4. Zymase

Identify product 'B' in the given reaction:

1.		2.
3.		4.

HCN not produce a chiral compound with:

1.		2.
3.		4.

An alkene “A” on reaction with O₃ and Zn - H₂O gives propanone and ethanal in an equimolar ratio. The addition of HCl to alkene “A” gives “B” as the major product. The structure of product “B” is:

1.		2.
3.		4.

Find the reason why carbonyl compounds undergo nucleophilic addition reactions.

1. The electrophilic carbonyl carbon forms a sigma bond with the nucleophile.

2. Electromeric effect.

3. Electronegativity difference of carbon and oxygen atoms.

4. None of the above

Carboxylic acids are more acidic than phenol and alcohol because of 

1. formations of dimers

2. highly acidic hydrogen

3. resonance stabilization of their conjugate base

4. intermolecular hydrogen bonding 

Acetaldehyde cannot exhibit

1. Iodoform test

2. Benedict's test

3. Lucas test

4. Tollen's test