The reagent 'R' in the given sequence of a chemical reaction is :
1. | HI | 2. | CuCN/KCN |
3. | H2O | 4. | CH3CH2OH |
Identify the compound that will react with Hinsberg's reagent to give a solid which dissolves in alkali.
1. | 2. | ||
3. | 4. |
The incorrect statement among the following is :
1. | pK b of aniline is more than methylamine. |
2. | Ethylamine is soluble in water whereas aniline is not. |
3. | Aniline undergo Friedel-Crafts reaction |
4. | Gabriel phthalimide synthesis is preferred for synthesizing primary amines. |
The incorrect statement among the following is :
1. | Acetylation is an example of a nucleophilic acyl substitution reaction. |
2. | In acetylation, amine reacts with an acid chloride, anhydrides, and esters. |
3. | Amines react with benzoyl chloride. The reaction is known as the coupling reaction. |
4. | Carboxylic acid reacts with amines and gives salts at room temperature. |
The correct statements among the following is :
1. | Coupling reaction is an example of an electrophilic substitution reaction. |
2. | Azo dye contains -N=N- linkage. |
3. | p-Aminoazobenzene is obtained when diazonium salt reacts with an aniline. |
4. | All of the above |
Consider the following statements related to ammonolysis.
a. | Cleavage of C-X bond by ammonia takes place. |
b. | Ammonolysis produces primary, secondary, tertiary amine and quaternary ammonium salt. |
c. | In ammonolysis, ammonia is a nucleophile. |
The true statement(s) are-
1. a, b
2. a, b, c
3. a, c
4. b
A and B in the above reaction sequence are -
Identify compounds A, B, and C
1. A = , B = , C =
2. A = , B = , C =
3. A = , B = , C =
4. A = , B = , C =
The molecular formulae of A and B in the following are:
\(CH_3CH_2Br\xrightarrow{KCN}CH_3CH_2CN\xrightarrow{LiAlH_4}\\ A\xrightarrow {HNO_2,~0 \ ^{o}C}B\)
1. \(\mathrm{{CH}_{3} {CH}_{2} {CH}_{2} {NH}_{2}}, ~\text{and} ~\mathrm{{CH}_{3} {CH}_{2} {CH}_{3}}\)
2. \(\mathrm{{CH}_{3} {CH}_{2} {CH}_{2} {NH}_{2}},~\text{and} ~\mathrm{{CH}_{3} {CH}_{2} {CH}_{2} {OH}}\)
3. \(\mathrm{{CH}_{3} {CH}_{2} {CH}={NH}}, ~\text{and} ~\mathrm{{CH}_{3} {CH}_{2} {CH}_{2} {OH}}\)
4. \(\mathrm{{CH}_{3} {CH}_{2} {CH}={NH}}, ~\text{and} ~\mathrm{{CH}_{3} {CH}_{2} {CH}_{3}}\)