The dihedral angle of the least stable conformer of ethane is:
1. | 60° | 2. | 0° |
3. | 120° | 4. | 180° |
An alkene ‘A’ on ozonolysis gives a mixture of ethanal and pentan-3-one.
The IUPAC name of ‘A’ is :
1. 3-Ethylpent-2-ene
2. 3-Ethylpent-2- yne
3. 2-Ethylpent-3-ene
4. 3-Ethylpent-4-yne
A compound possessing optical isomerism provided it has the molecular formula C7H16, would be:
1. | 2,3-Dimethyl pentane | 2. | 2,2-Dimethyl butane |
3. | 2-Methyl hexane | 4. | None of the above |
Arrange the following carbanions in order of their decreasing stability:
A. \(\mathrm{H}_3 \mathrm{C}-\mathrm{C} \equiv \mathrm{C}^{-}\)
B. \(\mathrm{H}-\mathrm{C} \equiv \mathrm{C}^{-}\)
C. \(\mathrm{H}_3 \mathrm{C}-\mathrm{\bar{C}H_2}\)
1. A>B>C
2. B>A>C
3. C>B>A
4. C>A>B
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 |
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 reagent used in the above conversion is:
1. Cr2O3
2. Alc. KOH
3. Red hot Fe
4. NaNH2/liq.NH3
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
Among the two isomers given above, the reason behind higher boiling point of one isomer as compared to the order is :
1. Cis - less polar than trans
2. Trans - more polar than cis
3. Cis - more intermolecular forces
4. Trans - more dipole-dipole interactions
The products formed after ozonolysis of Pent-2-ene are -
1. Ethanal, Methanal
2. Ethanal, Propanal
3. Ethanal, Butanal
4. Ethanal, Ethanal