The IUPAC name of X and Y in the following reaction sequence are:

Chlorobenzene HNO3, H2SO4 X H2/Pd Y

1. 1-Chloro-4-nitrobenzene, and Nitrobenzene

2. 1-Chloro-3-nitrobenzene, and 4-Chloroaniline

3. 1-Chloro-4-nitrobenzene, and 4-Chloroaniline

4. 1-Chloro-3-nitrobenzene, and Nitrobenzene

Subtopic:  Mechanism |
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Benzamide  Br2, NaOH A 2. H3PO21. HNO2 Benzene CH3Cl, AlCl3
B

A and B in the above reaction sequence are -

1. Chlorobenzene and aniline

2. Aniline and toluene

3. p-Methylaniline and chlorobenzene

4. None of the above

 

 

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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\(\small{\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{I} \xrightarrow[]{NaCN} \mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CN}\xrightarrow[]{{OH}^{-},Partial hydrolysis} A \xrightarrow[NaOH]{{Br}_2} \mathrm{B}}\)

The molecular formulae of A, and B in the above reaction are-

1. CH3CH2COOH, and CH3CH(Br)COOH
2. CH3CH2COOH, and CH3CH2COBr
3. CH3CH2CONH2, and CH3CH2NH2
4. CH3CH2CONH2, and CH3CH2CH2NH2

Subtopic:  Mechanism |
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The formula of A and B in the following reaction is -

C6H5N2Cl  CuCN C6H5CN  H2O /H+  A NH3 ,B

 1. C6H5COOH, and C6H5CONH2
2. C6H5COOH, and C6H5NH2
3. C6H5CH2NH2, and C6H5CH2N=NH
4. C6H5CH2NH2, and  C6H5CH2N=NH

Subtopic:  Amines - Preparation & Properties |
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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. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
2. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{OH}\)
3. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{NH}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{OH}\)
4. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{NH}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{3}\)

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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ANH3,  CH3CONH2 NaOBr BNaNO2/HCl CH3OH

A and B in the above reaction sequence are :

1. CH3CH2OH, and CH3CH2N2Cl
2. CH3COOH, and CH3CH2NH2
3. CH3COOH, and CH3NH2
4. CH3CH2Br, and CH3NH2

Subtopic:  Mechanism |
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C6H5NO2Sn/HCl AHNO2, 273K C6H5N2ClC6H5OH B

A and B in the above reaction sequence are -

1. C6H5N=NH, and  C6H6
2. C6H5NH2, and p-hydroxyazobenzene
3. C6H5N=NH, and  p-hydroxyazobenzene
4. C6H5NH2, and C6H5OH

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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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

Subtopic:  Amines - Preparation & Properties |
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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

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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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.

Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
 68%
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