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AUCHE 250: Organic Chemistry I

Nguồn ngoài

AUCHE 250: Organic Chemistry I

Chemistry
Tác giả
Brian Rempel
Nhà xuất bản
Augustana Faculty, University of Alberta
Nguồn
LibreTexts
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Đọc trực tuyến Tải PDF (nguồn mở)
Mục lục· 68 mục
  1. 01: Review
  2. 1.01: Atomic Structure - The Nucleus
  3. 1.02: Atomic Structure - Orbitals
  4. 1.03: Atomic Structure - Electron Configurations
  5. 1.04: Development of Chemical Bonding Theory
  6. 1.05: Describing Chemical Bonds - Valence Bond Theory
  7. 1.06: sp Hybrid Orbitals and the Structure of Methane
  8. 1.07: sp Hybrid Orbitals and the Structure of Ethylene
  9. 1.08: sp Hybrid Orbitals and the Structure of Acetylene
  10. 1.09: Noncovalent Interactions Between Molecules
  11. 1.10: Drawing Chemical Structures
  12. 1.11: Functional Groups
  13. 1.12: Formal Charges
  14. 1.13: Infrared (IR) Spectroscopy
  15. 1.14: Interpreting IR Spectra
  16. 02: Arrow Pushing
  17. 2.01: Polar Covalent Bonds - Electronegativity
  18. 2.02: Polar Covalent Bonds - Dipole Moments
  19. 2.03: Kinds of Organic Reactions
  20. 2.04: Using Curved Arrows in Polar Reaction Mechanisms
  21. 2.05: An Example of a Polar Reaction - Addition of HBr to Ethylene
  22. 2.06: Resonance
  23. 2.07: Rules for Resonance Forms
  24. 2.08: Drawing Resonance Forms
  25. 03: Acids and Bases
  26. 3.01: Acids and Bases - The Brnsted-Lowry Definition
  27. 3.02: Acids and Bases - The Lewis Definition
  28. 3.03: Acid and Base Strength
  29. 3.04: Predicting Acid-Base Reactions from pKa Values
  30. 3.05: Organic Acids and Organic Bases
  31. 3.06: Keto-Enol Tautomerism
  32. 04: Conformations
  33. 4.01: Conformational Analysis of Alkanes
  34. 4.02: Cycloalkanes and Their Relative Stabilities
  35. 4.03: Cyclohexane Conformations
  36. 4.04: Conformations of Disubstituted Cyclohexanes
  37. 05: Stereochemistry
  38. 5.01: The Reason for Handedness in Molecules - Chirality
  39. 5.02: Enantiomers and the Tetrahedral Carbon
  40. 5.03: Optical Activity
  41. 5.04: Sequence Rules for Specifying Configuration
  42. 5.05: Diastereomers
  43. 5.06: Meso Compounds
  44. 5.07: A Review of Isomerism
  45. 06: Substitutions
  46. 6.01: The SN2 Reaction
  47. 6.02: Characteristics of the SN2 Reaction
  48. 6.03: The SN1 Reaction
  49. 6.04: Characteristics of the SN1 Reaction
  50. 6.05: Carbocation Structure and Stability
  51. 07: Eliminations
  52. 7.01: An Overview of Elimination Reactions
  53. 7.02: Elimination Reactions- Zaitsev's Rule
  54. 7.03: Sequence Rules - The EZ Designation
  55. 7.04: Leaving Groups
  56. 7.05: The E2 Reaction and the Deuterium Isotope Effect
  57. 7.06: The E2 Reaction and Cyclohexane Conformation
  58. 7.07: The E1 and E1cB Reactions
  59. 08: Additions
  60. 8.01: Electrophilic Addition Reactions (EARs)
  61. 8.02: Addition of Hydrogen Halides to Symmetrical Alkenes
  62. 8.03: Alkene Asymmetry and Markovnikov's Rule
  63. 8.04: Hydration- Acid Catalyzed Addition of Water
  64. 8.05: Addition of Halogens
  65. 8.06: Formation of Halohydrins
  66. 8.07: Stability of Alkenes
  67. 8.08: Reduction of Alkynes
  68. 8.09: Hydration of Alkenes - Addition of HO by Hydroboration