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Organic Chemistry III

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Organic Chemistry III

The study of organic reactions includes the chemical synthesis of natural products, drugs, and polymers, and study of individual organic molecules in the laboratory and via theoretical (in silico) study. This is a textbook map of the chapters 25-30 of McMurry's "Organic Chemistry" textbook; it is not a copy of the original textbook, but is an original construction or remix of comparable OER content on LibreTexts to recreate its organization.

Organic ChemistryChemistry
Author
Layne Morsch et al.
Publisher
LibreTexts
Source
LibreTexts
Language
EN
Category
Basic Sciences
Read online Download PDF (open licence)
Contents· 80 sections
  1. 24: Amines and Heterocycles
  2. 24.00: Chapter Objectives
  3. 24.01: Naming Amines
  4. 24.02: Structure and Properties of Amines
  5. 24.03: Basicity of Amines
  6. 24.04: Basicity of Arylamines
  7. 24.05: Biological Amines and the Henderson-Hasselbalch Equation
  8. 24.06: Synthesis of Amines
  9. 24.07: Reactions of Amines
  10. 24.08: Reactions of Arylamines
  11. 24.09: Heterocyclic Amines
  12. 24.10: Spectroscopy of Amines
  13. 24.S: Amines and Heterocycles (Summary)
  14. 25: Carbohydrates
  15. 25.00: Introduction
  16. 25.01: Classification of Carbohydrates
  17. 25.02: Depicting Carbohydrate Stereochemistry - Fischer Projections
  18. 25.03: D L Sugars
  19. 25.04: Configurations of Aldoses
  20. 25.05: Cyclic Structures of Monosaccharides - Anomers
  21. 25.06: Reactions of Monosaccharides
  22. 25.07: The Eight Essential Monosaccharides
  23. 25.08: Disaccharides
  24. 25.09: Polysaccharides and Their Synthesis
  25. 25.10: Other Important Carbohydrates
  26. 25.11: Cell-Surface Carbohydrates and Influenza Viruses
  27. 25.S: Biomolecules- Carbohydrates (Summary)
  28. 26: Amino Acids Peptides and Proteins
  29. 26.00: Chapter Objectives
  30. 26.01: Introduction
  31. 26.02: Structures of Amino Acids
  32. 26.03: Amino Acids the Henderson-Hasselbalch Equation and Isoelectric Points
  33. 26.04: Synthesis of Amino Acids
  34. 26.05: Peptides and Proteins
  35. 26.06: Amino Acid Analysis of Peptides
  36. 26.07: The Edman Degradation
  37. 26.08: Peptide Synthesis
  38. 26.09: The Merrifield Solid-Phase Technique
  39. 26.10: Protein Structure
  40. 26.11: Enzymes and Coenzymes
  41. 26.12: How do Enzymes Work Citrate Synthase
  42. 27: Lipids
  43. 27.00: Introduction to Lipids
  44. 27.01: Waxes Fats and Oils
  45. 27.02: Soap
  46. 27.03: Phospholipids
  47. 27.04: Prostaglandins and Other Eicosanoids
  48. 27.05: Terpenoids
  49. 27.06: Steroids
  50. 27.07: Biosynthesis of Steroids
  51. 27.S: Biomolecules - Lipids (Summary)
  52. 28: Nucleic Acids
  53. 28.00: Chapter Objectives
  54. 28.01: Nucleotides and Nucleic Acids
  55. 28.02: Base Pairing in DNA - The Watson-Crick Model
  56. 28.03: Replication of DNA
  57. 28.04: Transcription of DNA
  58. 28.05: Translation of RNA - Protein Biosynthesis
  59. 28.06: DNA Sequencing
  60. 28.07: DNA Synthesis
  61. 28.08: The Polymerase Chain Reaction
  62. 29: Orbitals and Organic Chemistry - Pericyclic Reactions
  63. 29.00: Chapter Overview
  64. 29.01: Molecular Orbitals of Conjugated Pi Systems
  65. 29.02: Electrocyclic Reactions
  66. 29.03: Stereochemistry of Thermal Electrocyclic Reactions
  67. 29.04: Photochemical Electrocyclic Reactions
  68. 29.05: Cycloaddition Reactions
  69. 29.06: Stereochemistry of Cycloadditions
  70. 29.07: Sigmatropic Rearrangements
  71. 29.08: Some Examples of Sigmatropic Rearrangements
  72. 29.09: A Summary of Rules for Pericyclic Reactions
  73. 30: Synthetic Polymers
  74. 30.00: Chapter Objectives
  75. 30.01: Chain-Growth Polymers
  76. 30.02: Stereochemistry of Polymerization - Ziegler-Natta Catalysts
  77. 30.03: Copolymers
  78. 30.04: Step-Growth Polymers
  79. 30.05: Olefin Metathesis Polymerization
  80. 30.06: Polymer Structure and Physical Properties