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
Aspirin

What is Aspirin?


Aspirin is acetylsalicylic acid. It is prepared using salicylic acid (or 2-hydroxybenzoic acid ) reacting with acetic anhydride. 

Aspirin is a commonly orally administered non-steroidal antiinflammatory drug for the treatment of pain and fever or inflammation due to various causes.   It is sometimes used to treat or prevent heart attacks, strokes, and chest pain (angina). Aspirin should be used for cardiovascular conditions only under the supervision of a doctor. Acetylsalicylic acid binds to and acetylates serine residues in cyclooxygenases, resulting in decreased synthesis of prostaglandin, platelet aggregation, and inflammation.  It works by reducing substances in the body that causpain and fever and inflammation.

Aspirin  is perhaps the most commonly used analgesic and antipyretic medication worldwide, having been in clinical use for over 100 years. This drug also inhibits platelet aggregation and is used in the prevention of blood clots stroke, and myocardial infarction (MI). Interestingly, the results of various studies have demonstrated that long-term use of acetylsalicylic acid may decrease the risk of various cancers, including colorectal, esophageal, breast, lung, prostate, liver and skin cancer. Aspirin is classified as a non-selective cyclooxygenase (COX) inhibitor and is available in many doses and forms, including chewable tablets, suppositories, extended release formulations, and others. Acetylsalicylic acid is a very common cause of accidental poisoning in young children. It should be kept out of reach from young children, toddlers, and infants.  Aspirin can cause several forms of liver injury: in high doses, aspirin can cause moderate to marked serum aminotransferase elevations occasionally with jaundice or signs of liver dysfunction, and in lower doses in susceptible children with a febrile illness aspirin can lead to Reye syndrome.