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Tuesday, May 24, 2011

Khan Academy

Khan Academy

Organic Chemistry

Topics covered in college organic chemistry course. Basic understanding of basic high school or college chemistry assumed

  1. Representing Structures of Organic Molecules
  2. Naming Simple Alkanes
  3. Naming Alkanes with Alkyl Groups
  4. Correction - 2-Propylheptane should never be the name!
  5. Common and Systematic Naming-Iso, Sec and Tert Prefixes
  6. More Organic Chemistry Naming Examples 1
  7. Organic Chemistry Naming Examples 2
  8. Organic Chemistry Naming Examples 3
  9. Organic Chemistry Naming Examples 4
  10. Organic Chemistry Naming Examples 5
  11. Naming Alkenes Examples
  12. Naming Alkyl Halides
  13. sp3 Hybridized Orbitals and Sigma Bonds
  14. Pi bonds and sp2 Hybridized Orbitals
  15. Newman Projections
  16. Newman Projections 2
  17. Chair and Boat Shapes for Cyclohexane
  18. Double Newman Diagram for Methcyclohexane
  19. Introduction to Chirality
  20. Chiral Examples 1
  21. Chiral Examples 2
  22. Cahn-Ingold-Prelog System for Naming Enantiomers
  23. R,S (Cahn-Ingold-Prelog) Naming System Example 2
  24. Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds
  25. Cis-Trans and E-Z Naming Scheme for Alkenes
  26. Entgegen-Zusammen Naming Scheme for Alkenes Examples
  27. Introduction to Reaction Mechanisms
  28. Markovnikov's Rule and Carbocations
  29. Addition of Water (Acid-Catalyzed) Mechanism
  30. Polymerization of Alkenes with Acid
  31. Sn2 Reactions
  32. Sn1 Reactions
  33. Steric Hindrance
  34. Sn2 Stereochemistry
  35. Solvent Effects on Sn1 and Sn2 Reactions
  36. Nucleophilicity (Nucleophile Strength)
  37. Nucleophilicity vs. Basicity
  38. E2 Reactions
  39. E1 Reactions
  40. Zaitsev's Rule
  41. Comparing E2 E1 Sn2 Sn1 Reactions
  42. E2 E1 Sn2 Sn1 Reactions Example 2
  43. E2 E1 Sn2 Sn1 Reactions Example 3
  44. Free Radical Reactions
  45. Alcohols
  46. Alcohol Properties
  47. Resonance
  48. Ether Naming and Introduction
  49. Cyclic ethers and epoxide naming
  50. Ring-opening Sn2 reaction of expoxides
  51. Sn1 and Sn2 epoxide opening discussion
  52. Aromatic Compounds and Huckel's Rule
  53. Naming Benzene Derivatives Introduction
  54. Electrophilic Aromatic Substitution
  55. Bromination of Benzene
  56. Amine Naming Introduction
  57. Amine Naming 2
  58. Amine as Nucleophile in Sn2 Reaction
  59. Amine in Sn2 part 2
  60. Sn1 Amine Reaction
  61. Aldehyde Introduction
  62. Ketone Naming
  63. Friedel Crafts Acylation
  64. Friedel Crafts Acylation Addendum
  65. Keto Enol Tautomerization
  66. Carboxlic Acid Introduction
  67. Carboxylic Acid Naming
  68. Fisher Esterification
  69. Acid Chloride Formation
  70. Amides, Anhydrides, Esters and Acyl Chlorides
  71. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides
  72. Amide Formation from Acyl Chloride
  73. Aldol Reaction
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