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CHE 201: Organic Chemistry I

Nguồn ngoài

CHE 201: Organic Chemistry I

Chemistry
Tác giả
Hernan D. Biava
Nhà xuất bản
Brevard College
Nguồn
LibreTexts
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Đọc trực tuyến Tải PDF (nguồn mở)
Mục lục· 73 mục
  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)