Which isomer of pent-2-ene will have a higher boiling point and why?
1. Cis - less polar than trans
2. Trans - more polar than cis
3. Cis - more intermolecular forces
4. Trans - more dipole-dipole interactions
Decreasing order of acidic behavior of benzene, n-hexane, and ethyne is:
1. Hexane > Ethyne > Benzene
2. Benzene > Hexane > Ethyne
3. Ethyne > Benzene > Hexane
4. Benzene > Ethyne > Hexene
The reagent used in the above conversion is:
1. Cr2O3
2. Alc. KOH
3. Red hot Fe
4. NaNH2/liq.NH3

Out of the above alkenes, the ones that can give 2-methyl butane on hydrogenation are:
| 1. | a, b | 2. | b, c |
| 3. | a, c | 4. | a, b, c |
The correct order of decreasing reactivity of the following compounds:
Chlorobenzene, 2,4-Dinitrochlorobenzene, and p-Nitrochlorobenzene
with an electrophile (E+) is :
| 1. | Chlorobenzene > p–Nitrochlorobenzene > 2,4-Dinitrochlorobenzene |
| 2. | p – Nitro chlorobenzene > 2, 4-Dinitrochlorobenzene > Chlorobenzene |
| 3. | Chlorobenzene > 2, 4-Dinitrochlorobenzene > p-Nitrochlorobenzene |
| 4. | 2, 4-Dinitrochlorobenzene > Chlorobenzene > p-Nitrochlorobenzene |
The products formed after ozonolysis of Pent-2-ene are:
| 1. | Ethanal and Methanal | 2. | Ethanal and Propanal |
| 3. | Ethanal and Butanal | 4. | Ethanal and Ethanol |
What type of mechanism governs the chlorination reaction of methane?
1. Elimination
2. Substitution nucleophilic unimolecular (\(S_{N^1}\))
3. Free Radical
4. Substitution nucleophilic bimolecular ( \(S_{N^2}\))
The mechanism & intermediate involved in the above reaction are:
1. Aromatic electrophilic substitution & carbocation
2. Aromatic Nucleophilic substitution & carbanion
3. Aromatic free radical substitution & Free radical
4. Carbene based substitution reaction & Carbene
An unsaturated hydrocarbon 'A' reacts with two molecules of H2 and upon reductive ozonolysis A gives butane-1,4-dial, ethanal, and propanone.
The IUPAC name of A is:
1. 2-Methylocta-2,6-diene
2. 2-Methylocta-1,5-diene
3. 3-Methylocta-2,6-diene
4. 2-Methylocta-1,6-diene
The type of radicals that can be formed as intermediates during monochlorination of 2-methylpropane is-
1. Primary and tertiary radicals
2. Two types of primary radicals
3. Primary and secondary radicals
4. Two types of tertiary radical