The stability of 2,3-dimethyl but-2-ene is more than 2-butene. This can be explained in terms of:

1. Resonance

2. Hyperconjugation

3. Electromeric effect

4. Inductive effect

(CH₃)₄N⁺ is neither an electrophile nor a nucleophile because it:

Which of the following is an electrophilic reagent?

1. RO^-

2. BF₃

3. NH₃

4. RO····H

The-I effect is shown by:

1. -COOH

2. -CH₃

3. -CH₃CH₂

4. -CHR₂

Sulphur trioxide is:

1. an electrophile              2. a nucleophile

3. a homolytic agent          4. a base

Allyl isocyanide has:

1. 9σ and \(4\pi\) bonds.

2. 8σ and \(5\pi\) bonds.

3. 9σ, \(3\pi\) and 2 non-bonded electrons.

4. 8σ, \(3\pi\) and 4 non-bonded electrons.

The least stable resonance structure among the following is:

Hyperconjugation involves overlap of the following orbitals:

(1) σ - σ

(2) σ - p

(3) p - p

(4) π - π

Buta-1,3-diene and But-2-yne are:

1. position isomers

2. functional isomers

3. chain isomers

4. tautomers

In the following carbocations, the most stabile carbocation:

(1)  RCH₂C+H_{3         (2)} 

_{(3)                  (4)}