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AUCHE 250: Organic Chemistry I

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AUCHE 250: Organic Chemistry I

Chemistry
Author
Brian Rempel
Publisher
Augustana Faculty, University of Alberta
Source
LibreTexts
Language
EN
Category
Basic Sciences
Read online Download PDF (open licence)
Contents· 68 sections
  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