The IUPAC name of is:
1. Butane-2, 3-dial
2. Butane-1, 3-dione
3. Butane-2, 3-dione
4. 1, 2-dimethylethanedione
The IUPAC name of is:
1. 4-Bromo benzenamine
2. 4-Amino-1-bromobenzene
3. 4-Bromo benzenamide
4. 1-Bromo benzencarboxamide
The IUPAC name of is:
1. 2, 6-Dimethylhepta-2, 5-dienoic acid
2. 3, 7-Dimethylhepta-2, 5-dienoic acid
3. 1-Hydroxy-2, 6-dimethylhepta-2, 5-dienone
4. none of these
The most stable carbocation is:
1.
2.
3.
4.
The electromeric effect in organic compounds is a
1. temporary effect
2. permanent effect
3. temporary-permanent effect
4. none of the above
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:
1. | does not have an electron pair for donation as well as cannot attract an electron pair. |
2. | neither has an electron pair available for donation nor can accommodate electrons since all shells of N are fully occupied. |
3. | can act as Lewis acid and base. |
4. | none of the above. |
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