The order of reactivity of following alcohols with halogen acids is:
| I. | ![]() |
| II. | ![]() |
| III. | ![]() |
1. (I) >(II) > (III)
2. (III) > (II) > (I)
3. (II) >(I) > (III)
4. (I) >(III) > (II)
Which of the following alcohols will yield the corresponding alkyl chloride on reaction with concentrated HCl at room temperature?
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
Aniline undergoes diazotisation with NaNO₂ and HCl at 273–278 K.
The resulting diazonium salt is subsequently treated with cuprous chloride (Cu₂Cl₂).
Identify the major organic product (Y).
1. Chlorobenzene
2. Benzene
3. 1,3-Dichlorobenzene
4. 1,4-Dichlorobenzene
Toluene reacts with a halogen in the presence of iron (III) chloride giving ortho and para halo compounds. The reaction is:
1. Electrophilic elimination reaction
2. Electrophilic substitution reaction
3. Free radical addition reaction
4. Nucleophilic substitution reaction
The most suitable reagent for the following conversion is:
\(\begin{align} CH_3CH_2CH_2CH_3 \rightarrow\ & CH_3CH_2CH_2CH_2Cl\ +\ \\ & CH_3CH_2CHClCH_3\end{align} \)
1. Cl2/UV light
2. NaCl + H2SO4
3. Cl2 gas in the dark
4. Cl2 gas in the presence of iron in the dark
Arrange the following compounds in the increasing order of their densities:
![]() |
![]() |
![]() |
![]() |
| (i) | (ii) | (iii) | (iv) |
1. (i) < (ii) < (iii) < (iv)
2. (i) < (iii) < (iv) < (ii)
3. (iv) < (iii) < (ii) < (i)
4. (ii) < (iv) < (iii) < (i)
Arrange the following compounds in increasing order of their boiling points.
| (i) | ![]() |
| (ii) | ![]() |
| (iii) | ![]() |
1. (ii) < (i) < (iii)
2. (i) < (ii) < (iii)
3. (iii) < (i) < (ii)
4. (iii) < (ii) < (i)
Compound(s) among the following with an asterisk (*) asymmetric carbon is/are:

1. (a), (b), (c), (d)
2. (a), (b), (c)
3. (b), (c), (d)
4. (a), (c), (d)
Which of the following is an enantiomer of the given molecule?

| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
Which of the following is an example of vic-dihalide?
1. Dichloromethane
2. 1, 2-Dichloroethane
3. Ethylidene chloride
4. Allyl chloride