Chlorobenzene HNO3, H2SO4 X H2/Pd Y

X and Y in the above sequence are-

  • 1-chloro-4-nitrobenzene, and nitrobenzene

  •  1-chloro-3-nitrobenzene, and 4-chloroaniline

  •  1-chloro-4-nitrobenzene, and 4-chloroaniline

  •  1-chloro-3-nitrobenzene, and nitrobenzene

Benzamide  Br2, NaOH A 2. H3PO21. HNO2 Benzene CH3Cl, AlCl3B

A and B in the above reaction sequence are -

 

 

  • Chlorobenzene and aniline

  • Aniline and toluene

  • p-Methylaniline and chlorobenzene

  • None of the above

CH3CH2INaCNCH3CH2CNOH-, Partial hydrolysisANaOHBr2B

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

1. CH3CH2COOH, and CH3CH(Br)COOH2. CH3CH2COOH, and CH3CH2COBr3. CH3CH2CONH2, and CH3CH2NH24. CH3CH2CONH2, and CH3CH2CH2NH2

 

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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 C6H5CONH22. C6H5COOH, and C6H5NH23. C6H5CH2NH2, and C6H5CH2N=NH4. C6H5CH2NH2, and  C6H5CH2N=NH

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The molecular formulae of A and B in the following are-
\(CH_3CH_2Br\xrightarrow{KCN}CH_3CH_2CN\xrightarrow{LiAlH_4}\\A\xrightarrow {HNO_2,~OCo}B\)

  • \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
  • \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{OH}\)
  • \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{NH}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{OH}\)
  • \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}=\mathrm{NH}, and ~\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{3}\)

ANH3,  CH3CONH2 NaOBr BNaNO2/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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Identify compounds A, B, and C

 

 

 

 

 

 

 

  •      A  = ,  B =     , C =  

  •   A  = ,  B =     , C =  

  •  A  =   ,  B =   , C =  

  •  A  =   ,  B =   , C =  

C6H5NO2Sn/HCl AHNO2, 273K C6H5N2ClC6H5OH B

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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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-

  • a, b

  • a, b, c

  • a, c

  • b

The correct statements among the following is -

  • Coupling reaction is an example of an electrophilic substitution reaction.

  • Azo dye contains -N=N- linkage.

  • p-Aminoazobenzene is obtained when diazonium salt reacts with an aniline.

  • All of the above

The incorrect statement among the following is -

 

  •  pKb of aniline is more than methylamine.

  • Ethylamine is soluble in water whereas aniline is not.

  • Aniline undergo Friedel-Crafts reaction

  • Gabriel phthalimide synthesis is preferred for synthesizing primary amines.

Identify the compound that will react with Hinsberg's reagent to give a solid which dissolves in alkali.

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  •  

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The reagent 'R' in the given sequence of a chemical reaction is : 

  • HI

  • CuCN/KCN

  • H2O

  • CH3CH2OH

Aniline with excess of methyl iodide in the presence of sodium carbonate solution gives: 

  •  N, N-dimethylaniline.
  •  N, N-diethylaniline.
  •   N, N, N−triethylanilinium carbonate.

  •  N, N, N−trimethylanilinium carbonate.
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