Phu Xuan University Library
OCLUE: Organic Chemistry, Life, the Universe, and Everything

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OCLUE: Organic Chemistry, Life, the Universe, and Everything

Organic chemistry is the chemistry of carbon and carbon-containing compounds. Since the core structural, catalytic, information storage, and retrieval systems of organisms are carbon-based macromolecules, organic chemistry is of direct relevance to the life sciences. Just as importantly, the properties of carbon make possible an amazing range of molecules with unique properties, from small molecules to complex plastics and even more complex biomolecules.

Author
Melanie M. Cooper & Michael W. Klymkowsky
Publisher
LibreTexts
Source
LibreTexts
License
CC BY-NC-SA
Language
EN
Category
Basic Sciences
Contents· 78 sections
  1. 01: AcidBase Reactions
  2. 1.01: A Quick Review of the Models of Acid-Base Reactions.
  3. 1.02: Acid-Base Reaction Direction and Position of Equilibrium
  4. 1.03: Effect of pH on Acid Base Reactions
  5. 1.04: Lewis Acids and Bases Electrophiles and Nucleophiles
  6. 1.05: In-Text References
  7. 02: Spectroscopy- how we know what we know about the structure of matter
  8. 2.01: Interactions of Electromagnetic Radiation and Electrons in Molecules
  9. 2.02: UV-Vis Spectroscopy and Chormophores - or Why are Carrots Orange
  10. 2.03: Infrared (IR) Spectroscopy - Looking at Molecular Vibrations
  11. 2.04: Functional Groups
  12. 2.05: Carbon-13 NMR Spectroscopy
  13. 2.06: H-1 (proton) NMR
  14. 2.07: In-Text References
  15. 03: Conformations and Configurations - the consequences of the three-dimensional nature of carbon compounds
  16. 3.01: Conformations of Organic Molecules
  17. 3.02: Optical Isomerism
  18. 3.03: Configurations of Chiral Molecules- the Cahn-Ingold-Prelog Convention
  19. 3.04: In-Text References
  20. 04: Nucleophilic Substitution Part II
  21. 4.01: Kinetics and Mechanisms-
  22. 4.02: The (mathrmS mathrmN 1) Reaction
  23. 4.03: Rearrangements- A Consequence of Generating Unstable Carbocations
  24. 4.04: Eliminations
  25. 4.05: In-Text References
  26. 05: Alkenes and Alkynes
  27. 5.01: Reactions of Alkenes- Electrophilic Addition
  28. 5.02: Anti-Markovnikov Addition across Double Bonds
  29. 5.03: Reduction of Alkenes-
  30. 5.04: Oxidation of Alkenes
  31. 5.05: Reactions of Alkynes
  32. 5.06: In-Text References
  33. 06: Alcohols and an introduction to thiols amines ethers and sulfides
  34. 6.01: (Brnsted) Acidity of Alcohols Thiols and Amines
  35. 6.02: Nucleophilicity of (mathrmROH) (mathrmRSH) and (mathrmRNH 2)
  36. 6.03: (mathrmO) (mathrmS) and (mathrmN) as Leaving Groups
  37. 6.04: Oxidation of Alcohols
  38. 6.05: Oxidation of Thiols
  39. 6.06: Preparation of Alcohols
  40. 6.07: In-Text References
  41. 07: Nucleophilic attack at the carbonyl carbon-
  42. 7.01: Interconversion of Acids and Derivatives- Predicting Outcomes
  43. 7.02: Preparations of Carboxylic Acids
  44. 7.03: The Wittig Reaction
  45. 7.04: Synthesis
  46. 7.05: In-Text References
  47. 7.06: Aldehydes and Ketones
  48. 7.07: Nucleophilic Attack by Hydride or Carbanions
  49. 7.08: Reactions of Aldehydes and Ketones with Oxygen Nucleophiles
  50. 7.09: Reactions with Nitrogen Nucleophiles
  51. 7.10: Carboxylic Acids and Derivatives
  52. 7.11: Infra-red Spectra as Evidence of Carboxylic Acid Derivative Structure
  53. 7.12: Relative Reactivities of Carboxylic Acids and Derivatives
  54. 7.13: Reactions at the Carbonyl Group of Acid Derivatives with Irreversible Nucleophiles
  55. 7.14: Nucleophilic Addition and Elimination Reactions of Acids and Derivatives
  56. 08: Conjugated compounds and aromaticity
  57. 8.01: Reactions of Substituted Benzenes- Reaction at the Benzylic Position
  58. 8.02: Pericyclic reactions
  59. 8.03: In-Text References
  60. 8.04: UV-VIS Spectroscopy and Conjugated Systems- Review
  61. 8.05: Aromaticity
  62. 8.06: What is aromaticity and how do we recognize aromatic systems
  63. 8.07: Aromatic Ions
  64. 8.08: Heterocyclic Aromatic Compounds
  65. 8.09: Spectroscopy of Aromatic Compounds-
  66. 8.10: Reactions of Aromatic Compounds- Introduction of one group onto the ring
  67. 8.11: Multiple Substituents- Directing Effects
  68. 8.12: Nucleophilic Substitutions on Aromatic Systems- Expanding the range of potential substitution products
  69. 09: A return to the carbonyl
  70. 9.01: Reactions of Enols and Enolates
  71. 9.02: The Aldol Reaction
  72. 9.03: The Claisen Condensation
  73. 9.04: -Ketoacids Decarboxylate
  74. 9.05: Biosynthesis of Fatty Acids-
  75. 9.06: Michael Reactions
  76. 9.07: Glycolysis
  77. 9.08: Glycolysis- From Glucose to Fructose
  78. 9.09: In-Text References