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Textbook Map: Brown/Foote/Iverson/Anslyn

  • Page ID
    7879
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    1. Covalent Bonding and Shapes of Molecules.
    2. Alkanes and Cycloalkanes.
    3. Stereochemistry and Chirality.
    4. Acids and Bases.
    5. Alkenes.
    6. Reactions of Alkenes.
      • 6.1 Reactions of Alkenes— An Overview
      • 6.2 Organic Reactions Involving Reactive Intermediates
      • 6.3 Electrophilic Additions
      • 6.4 Hydroboration-Oxidation
      • 6.5 Oxidation How To Write a Balanced Half-Reaction
      • 6.6 Reduction
      • 6.7 Molecules Containing Chiral Centers as Reactants or Products
    7. Alkynes.
    8. Haloalkanes, Halogenation, and Radical Reactions.
    9. Nucleophilic Substitution and B-Elimination.
    10. Alcohols.
    11. Ethers, Sulfides, and Epoxides.
    12. Infrared Spectroscopy.
    13. Nuclear Magnetic Resonance Spectroscopy.
    14. Mass Spectrometry.
    15. Introduction to Organometallic Compounds.
    16. Aldehydes and Ketones.
    17. Carboxylic Acids.
    18. Functional Derivatives of Carboxylic Acids.
    19. Enolate Anions and Enamines.
    20. Dienes, Conjugated Systems, and Pericyclic Reactions.
    21. Benzene and the Concept of Aromaticity.
    22. Reactions of Benzene and Its Derivatives.
    23. Amines.
    24. Catalytic Carbon–Carbon Bond Formation.
    25. Carbohydrates.
    26. Lipids.
    27. Amino Acids and Proteins.
    28. Nucleic Acids.
    29. Organic Polymer Chemistry.

    Appendices:

    1. Thermodynamics and the Equilibrium Constant.
    2. Major Classes of Organic Acids.
    3. Bond Dissociation Enthalpies.
    4. Characteristic 1H-NMR Chemical Shifts.
    5. Characteristic 13C Chemical Shifts.
    6. Characteristic IR Absorption Frequencies.
    7. Electrostatic Potential Maps.
    8. Summary of Stereochemical Terms.
    9. Summary of the Rules of Nomenclature.
    10. Common Mistakes in Arrow Pushing.
    11. Organic Chemistry Roadmaps

    Textbook Map: Brown/Foote/Iverson/Anslyn is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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