1. Physical chemistry
    2. 1. The solid state
    2. Language of Chemistry
    3. Gaseous and Liquid states
    4. Stoichiometry
    5. Solutions
    6. Structure of Atom
    7. Chemical equilibrium
    8. Nuclear chemistry (Radioactivity)
    9. Ionic equilibrium
    10. Chemical Bonding
    11. Chemical kinetics
    12. Concepts of Acids, Bases and Salts
    13. Surface catalysis and Colloids
    14. Redox reactions
    15. Chemical energetics
    16. Volumetric analysis
    17. Electrochemistry
  2. Inorganic chemistry
    3. 18. Introduction
    19. Periodic table
    20. Hydrogen and its compounds
    21. General aspects of Metallergy
    22. Alkali metals
    23. Alkaline metals
    24. Boron family
    25. Carbon family
    26. Nitrogen family
    27. Oxygen family
    28. Fluorine family
    29. Inert gases
    30. Transition metals
    31. Coordination compounds
    32. Analytical chemistry
  3. Organic chemistry
    4. 33. Purification and analysis of organic compounds
    34. Nomenclature of Organic compounds
    35. Reaction Mechanisms
    36. Hydrocarbons
    37. Haloalkanes (Alkyl halides)
    38. Alcohol, Phenol and Ether
    39. Aldehyde and Ketones
    40. Carboxylic acids
    41. Compounds conatining Nitrogen
    42. Polymers
    43. Chemistry in daily life
Organic chemistry
41. Compounds conatining Nitrogen
1. The process in which amides are changed into amines is called

[TOM 2007]

  • Friedel-Crafts reaction
  • Wurtz reaction
  • Hoffmann's reaction
  • Williamson's reaction
2. Aniline is converted into benzanilide by reacting with

[IOM 2002]

  • Benzoyl chloride
  • Chlorobenzene
  • Benzyl chloride
  • Phenyl chloride
3. Nitrobenzene forms aniline by

[IOM 2002]

  • Addition reaction
  • Reduction reaction
  • Substitution reaction
  • All
4. The reduction of nitrobenzene in acid medium gives

[IOE]

  • Benzene
  • Dinitrobenzene
  • Aniline
  • Phenol
5. Benzene reacts with mixture of conc. H₂SO₄ + HNO₃ to form

[IOE]

  • Phenol
  • Nitrobenzene
  • Benzene sulphonic acid
  • Sulphonitrobenzene
6. When nitrobenzene is treated with zinc dust and aqueous ammonium chloride, we get

[MOE Curriculum 2008]

  • Aniline
  • Phenyl hydroxylamine
  • Azoxybenzene
  • Hydrazobenzene
7. The compound that gives positive arylamine reaction is

[MOE Curriculum]

  • (CH₃)₂NH
  • (CH₃)₃N
  • (CH₃)₂N⁺
  • CH₃NH₂
8. When nitrobenzene is reduced under alkaline conditions using zinc and NaOH, the final product obtained is

[MOE 2065]

  • Phenyl hydroxylamine
  • Nitrosobenzene
  • Aniline
  • Hydrazobenzene
9. Carbylamine reaction is given by

[MOE 2065, KU]

  • Primary amine
  • Secondary amine
  • Tertiary amine
  • All three types of amine
10. Bromination of Aniline gives

[MOE 2008, 063]

  • m-Bromoaniline
  • o-Bromoaniline
  • o,p-Dibromoaniline
  • 2,4,6-Tribromoaniline
11. When nitrobenzene is reacted with NH₄Cl and water, the product formed is

[MOE 2055]

  • Nitrobenzene
  • Phenylhydroxylamine
  • Aniline
  • Azoxybenzene
12. Ethyl chloride on heating with silver cyanide forms a compound 'X'. The compound 'X' is

[BPKIHS]

  • C₂H₅OH
  • C₂H₅CN
  • C₂H₅NH₂
  • C₂H₅NC