A→NH3,∆CH3CONH2→NaOBrB→NaNO2/HClCH3OH A And B In ...
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A→NH3, ∆ CH3CONH2 →NaOBr B→NaNO2/HCl CH3OH
A and B in the above reaction sequence are :
1. CH3CH2OH, and CH3CH2N2Cl2. CH3COOH, and CH3CH2NH23. CH3COOH, and CH3NH24. CH3CH2Br, and CH3NH2
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1. A = , B = , C =
2. A = , B = , C =
3. A = , B = , C =
4. A = , B = , C =
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A and B in the above reaction sequence are -
1. C6H5N=NH, and C6H62. C6H5NH2, and p-hydroxyazobenzene3. C6H5N=NH, and p-hydroxyazobenzene4. C6H5NH2, and C6H5OH
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Save changesSubtopic: Diazonium Salts: Preparation, Properties & Uses | 78%From NCERTOther Reason
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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
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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 |
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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. |
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Save changesSubtopic: Identification of Primary, Secondary & Tertiary Amines | 68%From NCERTOther Reason
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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. |
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1. | 2. | ||
3. | 4. |
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1. | HI | 2. | CuCN/KCN |
3. | H2O | 4. | CH3CH2OH |
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