obtained by chlorination of n-butane, will be:
1. Meso form
2. Racemic mixture
3. d-form
4. l-form
An organic compound A in reaction with Na/diethyl ether gives a hydrocarbon which on monochlorination gives only one chloro derivative. A is:
1. t-butyl chloride
2. sec. butyl chloride
3. Iso butyl chloride
4. n-butyl chloride
\(CH_3CH_2CHCl_2\) upon reaction with \(NaNH_2\)gives:
1. | 2. | ||
3. | 4. |
Given below is a reaction sequence:
\(\begin{aligned} & CH_3CH_2Cl\xrightarrow{NaCN}X\xrightarrow{H_2/Ni}Y\\ &Y\xrightarrow{\text{Acetic Anhydride}}Z \end{aligned}\)
Z in the above reaction is:
1. CH3CH2CH2NHCOCH3
2. CH3CH2CH2NH2
3. CH3CH2CH2CONHCH3
4. CH3CH2CH2CONHCOCH3
The reactivity order of halides for dehydrohalogenation is:
1. R–F > R–Cl > R–Br > R–I
2. R–I > R–Br > R–Cl > R–F
3. R–I > R–Cl > R–Br > R–F
4. R–F > R–I > R–Br > R–Cl
The –OH group of an alcohol or the carboxylic acid can be replaced by – Cl using:
1. | Hypochlorous acid | 2. | Chlorine |
3. | Hydrochloric acid | 4. | Phosphorous pentachloride |
Find the correct sequence of the bond enthalpy of the "C-X" bond among the following:
1. CH3-F < CH3-Cl > CH3-Br > CH3-I
2. CH3-Cl > CH3-F > CH3-Br > CH3-I
3. CH3-F < CH3-Cl < CH3-Br < CH3-I
4. CH3-F > CH3-Cl > CH3-Br > CH3-I
Which of the following undergoes nucleophilic substitution exclusively by SN1 mechanism?
1. Ethyl chloride
2. Isopropyl chloride
3. Benzyl chloride
4. Chlorobenzene
Consider the reactions:
(i) | \(\small{{(CH_3)}_2CHCH_2Br\ \xrightarrow[]{C_2H_5OH}{(CH_3)}_2CHCH_2OC_2H_5 + HBr}\) |
(ii) | \(\small{{(CH_3)}_2CHCH_2Br\ \xrightarrow[]{C_2H_5O^-}{(CH_3)}_2CHCH_2OC_2H_5 + Br^-}\) |
The mechanisms of reactions (i) and (ii) are, respectively: