目录

  • 1 Introduction
    • 1.1 General information about organic chemistry
    • 1.2 The nature of covalent bonds
    • 1.3 Structures of molecules
    • 1.4 Conjugative effects
    • 1.5 Chemical reactions
    • 1.6 PPT
    • 1.7 Online test
    • 1.8 literaures reading
  • 2 Alkanes
    • 2.1 Structures of Alkanes
    • 2.2 Nomenclature of Alkanes
    • 2.3 Isomerism of Alkanes
    • 2.4 Properties of Alkanes
    • 2.5 PPT
    • 2.6 Online test
  • 3 Cycloalkanes
    • 3.1 Isomerism of cycloalkanes
    • 3.2 Nomenclature of cycloalkanes
    • 3.3 Chemical Properties of Cycloalkanes
    • 3.4 Conformations of Cyclohexane
    • 3.5 PPT
    • 3.6 Online test
    • 3.7 literatures reading
  • 4 Stereochemistry
    • 4.1 Stereoisomerism
    • 4.2 Chirality
    • 4.3 R, S naming system
    • 4.4 Chirality in chemical reactions
    • 4.5 PPT
    • 4.6 Online test
    • 4.7 literatures reading
  • 5 Alkenes
    • 5.1 Nomenclature of Alkenes
    • 5.2 Isomerism of  Alkenes
    • 5.3 Chemical Reactions of Alkenes
      • 5.3.1 Addition of Hydrogen Halides to Alkenes and Carbocation Rearrangements
      • 5.3.2 Electrophilic Addition of Alkenes with H2O,HOR,H2SO4
      • 5.3.3 Halogenation
      • 5.3.4 Hydroboration-Oxidation of Alkenes
      • 5.3.5 Oxidation of Alkenes
      • 5.3.6 Hydrogenation of Alkenes
      • 5.3.7 Radical Addditon of HBr to Alkenes
      • 5.3.8 alpha-Hydrogen of  Alkenes
    • 5.4 Preparation of Alkenes
    • 5.5 Dienes
    • 5.6 Electrophilic addition reactions
    • 5.7 Other reactions of alkenes
    • 5.8 PPT
    • 5.9 Online test
    • 5.10 literatures reading
  • 6 Alkynes
    • 6.1 Nomenclature of Alkynes
    • 6.2 Chemical Reactions of Alkynes
      • 6.2.1 Electrophilic Addition  Reactions of Alkynes
      • 6.2.2 Oxidation Reactions of Alkynes
      • 6.2.3 Reduction Reactions of Alkynes
      • 6.2.4 Weak Acidity of Terminal Alkynes
    • 6.3 Preparation of Alkynes
    • 6.4 PPT
    • 6.5 Online test
  • 7 Organohalides
    • 7.1 Structure, Classification and Nomenclature of Organohalides
    • 7.2 Chemical Reactions
      • 7.2.1 Nucleophilic Substitution Reactions
      • 7.2.2 Elimination Reactions
      • 7.2.3 Other Chemical Reactions
    • 7.3 Mechanisms of Nucleophilic substitution reactions
      • 7.3.1 SN2 Mechanism
      • 7.3.2 SN1 Mechanism
    • 7.4 Mechanisms of Elimination Reactions
    • 7.5 Competing reactions of substitution and elimination reactions
    • 7.6 Preparation of Halohydrocarbons
    • 7.7 PPT
    • 7.8 Online test
    • 7.9 literatures reading
  • 8 Aromatic hydrocarbons
    • 8.1 Aromatic compounds
    • 8.2 Nomenclature of Benzene Derivatives
    • 8.3 Electrophilic Substitution of Benzene
      • 8.3.1 Halogenation
      • 8.3.2 Nitration
      • 8.3.3 Sulfonation
      • 8.3.4 F-C alkylation and acylation
    • 8.4 Substituent Effects
    • 8.5 Reduction reactions
    • 8.6 Side Chain Reactions  of Alkylbenzene
    • 8.7 Other Aromatic Compounds
    • 8.8 Aromaticity
    • 8.9 PPT
    • 8.10 Online test
    • 8.11 Literatures reading
  • 9 Alcohols and Phenols
    • 9.1 PPT
    • 9.2 Summary of Reactions
      • 9.2.1 Reactions of alcohols
      • 9.2.2 Reactions of phenols
    • 9.3 Synthesis of alcohols
    • 9.4 Aspirin
    • 9.5 literatures reading
    • 9.6 Online test
  • 10 Ethers
    • 10.1 PPT
    • 10.2 Summary of Reactions
    • 10.3 Synthesis of ethers
    • 10.4 Online test
  • 11 Aldehydes and ketones
    • 11.1 PPT
    • 11.2 Summary of Reactions
    • 11.3 Wolff-Kishner-Huang Minlon reaction
    • 11.4 literatures reading
    • 11.5 Online test
  • 12 Carboxylic acids
    • 12.1 PPT
    • 12.2 Summary of Reactions
    • 12.3 Preparation of carboxylic acids
    • 12.4 Online test
  • 13 Carboxylic acid derivatives
    • 13.1 PPT
    • 13.2 Summary of Reactions
    • 13.3 Online  test
  • 14 Amines
    • 14.1 PPT
    • 14.2 Summary of Reactions
    • 14.3 Preparation of amines
    • 14.4 Toxicity of N-nitros amines
    • 14.5 Online test
  • 15 Heterocycle compounds
    • 15.1 PPT
    • 15.2 Online test
Toxicity of N-nitros amines

Toxicity of N-nitros Amines

                               

-nitrosamines are aliphatic or aromatic derivatives of secondary amines, which have a nitroso (–NO) group attached to nitrogen. They are formed by the reaction of nitrite with secondary amines.  It was discovered that secondary amines present naturally in the fish had reacted with the nitrite to form NDMA, which had induced cancers in the livers of the mink. Human exposure to nitrosamines can result from formation of N‑nitroso compounds either in food during storage or preparation or in vivo, usually in the stomach. 

The toxicity of N -nitrosamines came to light in the mid-1950s when it was found that mink fed with herring meal that had been treated with nitrite were dying from liver disease.