\(CH_3CH_2CHCl_2\) upon reaction with \(NaNH_2\)gives:
1. | 2. | ||
3. | 4. |
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
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
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.
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 |
Which of the following undergoes nucleophilic substitution exclusively by SN1 mechanism?
1. Ethyl chloride
2. Isopropyl chloride
3. Benzyl chloride
4. Chlorobenzene