An organic compound A, having molecular formula C₄H₉Cl, reacts with sodium in dry diethyl ether to give a hydrocarbon.
This hydrocarbon on monochlorination gives only one chloro derivative.
Identify compound A.
1. t-Butyl chloride
2. sec. Butyl chloride
3. Iso butyl chloride
4. n-Butyl chloride
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
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
\(CH_3CH_2CHCl_2\) upon reaction with \(NaNH_2\) gives:
| 1. | 2. | ||
| 3. | 4. |
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 |
Chloropicrin is obtained by the reaction of:
1. Nitric acid on chlorobenzene.
2. Chlorine on picric acid.
3. Nitric acid on chloroform.
4. Steam on carbon tetrachloride.