Phu Xuan University Library
CHE 201: Organic Chemistry I

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CHE 201: Organic Chemistry I

Author
Hernan D. Biava
Publisher
Brevard College
Source
LibreTexts
Language
EN
Category
Basic Sciences
Contents· 73 sections
  1. 01: Introduction to Organic Chemistry
  2. 1.01: Organic Compounds
  3. 1.02: The Functional Group
  4. 1.03: Covalent Bonds
  5. 1.04: Bonding in Organic Molecules
  6. 1.05: Structural Isomerism in Organic Molecules
  7. 1.06: How to Draw Organic Molecules
  8. 02: Alkanes and Cycloalkanes
  9. 2.01: Structures and Names of Alkanes
  10. 2.02: Branched-Chain Alkanes
  11. 2.03: Condensed Structural and Skeletal Formulas
  12. 2.04: IUPAC Nomenclature
  13. 2.05: Halogenated Hydrocarbons
  14. 2.06: Conformations of Ethane
  15. 2.07: Conformations of Other Alkanes
  16. 2.08: Source of hydrocarbons- crude oil and natural gas
  17. 2.09: Cycloalkanes
  18. 2.10: Naming Cycloalkanes
  19. 2.11: Stability of Cycloalkanes - Ring Strain
  20. 2.12: Cis-Trans Isomerism in Cycloalkanes
  21. 2.13: Conformations of Cyclohexane
  22. 2.14: Axial and Equatorial Bonds in Cyclohexane
  23. 2.15: Conformations of Monosubstituted Cyclohexanes
  24. 2.16: Conformations of Disubstituted Cyclohexanes
  25. 2.17: Physical Properties of Alkanes
  26. 2.18: Reactions of Alkanes
  27. 2.19: Reaction Mechanism for Free-Radical Halogenation of Alkanes
  28. 03: Unsaturated Hydrocarbons
  29. 3.01: Alkenes- Structures and Names
  30. 3.02: Bonding in Ethene
  31. 3.03: Cis-Trans Isomers (Geometric Isomers)
  32. 3.04: Physical Properties of Alkenes
  33. 3.05: Chemical Properties of Alkenes
  34. 3.06: Alkene Asymmetry and Markovnikov's Rule
  35. 3.07: Polymerization
  36. 3.08: Polymerization Mechanism
  37. 3.09: Alkynes
  38. 3.10: Bonding in Ethyne
  39. 3.11: Physical Properties of Alkynes
  40. 3.12: Chemical properties of Alkynes
  41. 04: Aromatic Compounds (Arenes)
  42. 4.01: Aromatic Compounds- Benzene
  43. 4.02: Aromaticity
  44. 4.03: Bonding and Physical Properties of Arenes
  45. 4.04: Nomenclature of Aromatic Compounds
  46. 4.05: Polycyclic Aromatics
  47. 4.06: Carbon Nanomaterials
  48. 4.07: Chemical Properties of Aromatic Compounds
  49. 4.08: General Mechanism for Electrophilic Substitution Reactions of Benzene
  50. 4.09: Halogenation Sulfonation and Nitration of Aromatic Compounds
  51. 4.10: Alkylation and Acylation of Aromatic Rings - The Friedel-Crafts Reaction
  52. 4.11: Electrophilic Aromatic Substitution Reactions of Benzene Derivatives
  53. 4.12: Heterocyclic Aromatic Compounds
  54. 05: Stereochemistry
  55. 5.01: Chirality
  56. 5.02: Fischer Projections to communicate Chirality
  57. 5.03: Absolute Configuration and the (R) and (S) System
  58. 5.04: The E Z System for alkenes
  59. 5.05: Diastereomers - more than one chiral center
  60. 5.06: Meso Compounds
  61. 5.07: Isomerism Summary
  62. 5.08: Optical Activity Racemic Mixtures and Separation of Chiral Compounds
  63. 5.09: Resolution (Separation) of Enantiomers
  64. 5.10: Biochemistry of Enantiomers
  65. 06: Alcohols Phenols Ethers and Thiols
  66. 6.01: Alcohols - Nomenclature and Classification
  67. 6.02: Physical Properties of Alcohols
  68. 6.03: Reactions of Alcohols
  69. 6.04: Oxidation and Reduction in Organic Chemistry
  70. 6.05: Glycols and Glycerol
  71. 6.06: Phenols
  72. 6.07: Ethers
  73. 6.08: Thiols (Mercaptans)