A given nitrogen-containing aromatic compound a reacts with Sn/HCl, followed by HNO2 to give an unsatable compound B.B, on treament with phenol, forms a beautiful coloured compound C with the molecular formula C12H10N2O. The structure of compound A is

 

  • 1
  • 2
  • 3
  • 4

The following reaction, 

is known by the name:

  • Friedel-Crafts reaction

  • Perkins reaction

  • Acetylation reaction

  • Schotten-Baumann reaction

Which of the following will be most stable diazonium salt RN2+X- ?

  •  CH3N2+X-

  •  C6H5N2+X-

  •  CH3CH2N2+X-

  •  C6H5CH2N2+X-

In a reaction of aniline a coloured product C was obtained.

The structure of C would be

  • () 

  • () 

  • () 

  • () 

Which one of the following is an amine hormone ?

  • Thyroxine

  • Oxypurin

  • Insulin

  • Progesterone

The correct increasing order of basic strength for the following compounds is: 

  • III<I<II
  • III<II<I
  • II<I<III
  • II<III<I

Nitration of aniline in strong acidic medium also gives m-nitroaniline because -

  • In spite of substituents nitro group always goes to only m-position

  • In electrophilic substitution reactions amino group is meta directive

  • In absence of substituents nitro group always goes to only m-position

  • In acidic (strong) medium aniline is present as anilinium ion

A nitro-compounds among the following that does not react with nitrous acid is--

  •  

  •  

  •  

The correct statement regarding the basicity of arylamines is -

  • Arylamines are generally more basic than alkylamines because the lone-pair electrons of nitrogen are not delocalized by interaction with the aromatic ring π-electron system
  • Arylamines are generally more basic than alkylamines because of aryl group +I effect
  • Arylamines are generally more basic than alkylamines because the nitrogen atom in arylamines is sp-hybridized
  • Arylamines are generally less basic than alkylamines because the nitrogen lone-pair electrons are delocalized by interaction with the aromatic ring π-electron system.

The number of structural isomers possible from the molecular formula C3H9N is

  • 4

  • 5

  • 2

  • 3

Aniline cannot be prepared by -

  • Hydrolysis of phenyl isocyanide with an acidic solution

  • Degradation of benzamide with bromine in alkaline Solution

  • Reduction of nitrobenzene with H2/Pd in ethanol

  • Potassium salt of phthalimide treated with chlorobenzene followed by the hydrolysis aqueous NaOH solution

The electrolytic reduction of nitrobenzene in a strongly acidic medium produces-
 



 

  • p-Aminophenol
  • Azoxybenzene
  • Azobenzene
  • Aniline
  •  
     A in the above reaction, is:
     
     
     
     
    Nitrobenzene on reaction with conc. HNO3 /H2SO4 at 80 – 100 ºC forms -
     
     
     
     


    The product formed in the above mentioned reaction is -

    Aniline gives a set of the following reactions that yielded a colored product 'Y'. 

    273-278 KNaNO2/HClXN,N-dimethylanilineY

    The structure of 'Y' is -


      +NaNO2+HClProduct     

    The product formed in the above-mentioned reaction is -

     
    The structure of C in the above mentioned reaction is -

    In a set of reactions propanoic acid yielded a compound D

    CH3CH2COOHSOCl2BNH3CBr2KOHD 
    The structure of D would be :

    A compound that has higher basic character than aniline among the following is -

    The correct order of the basic strength of methyl substituted amines in aqueous solution is:

    NH2OHXNa/C2H5OHY

     Y in the above mentioned sequence is -

    Which of the following compounds will not give Hoffmann bromamide reaction?

    Which of the following substituent as 'X' not decreases the rate of reaction w.r.t. aniline?

    Which of the following compounds will give isocyanide test with CHCl3/KOH?

    Give the incorrect order of basic strength

    For the following reaction

    (major product) will be

    The product X and Y in the following reaction sequence is

    In this reaction sequence

    The major product 'S' of the following reaction sequence is

    Br2/FePSn/HClQexcess Br2/H2ORCuBr,HBrNaNO2-H2SO4/0°CS

    0:0:1


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