Oregon Institute of Technology: CHE 331 Organic Chemistry I

by Travis Lund

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Publisher
Oregon Institute of Technology
Subjects
Chemistry
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CC BY-NC-SA 4.0, as LibreTexts states it. Non-commercial use only.
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Tweens profiles and older, judged from its title and subjects

Contents

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  1. Front Matter
  2. TitlePage
  3. InfoPage
  4. Table of Contents
  5. Licensing
  6. 1: General Chemistry Recap
  7. 1.0: Prelude to Atoms, Electron Configurations, and Lewis Structures
  8. 1.1: Drawing Organic Structures
  9. 1.2: Valence Bond Theory
  10. 2: Functional Groups
  11. 2.0: Functional groups and organic nomenclature
  12. 2.1: Prelude to Organic Structure and Bonding II
  13. 3: Properties and Principles
  14. 3.0: Non-covalent interactions
  15. 3.1: Physical properties of organic compounds
  16. 3.2: Resonance
  17. 3.3: Molecular orbital theory- conjugation and aromaticity
  18. 4: Conformations and Stereochemistry
  19. 4.0: Prelude to Conformations and Stereochemistry
  20. 4.1: Conformations of open-chain organic molecules
  21. 4.2: Conformations of cyclic organic molecules
  22. 4.3: Chirality and stereoisomers
  23. 4.4: Naming chiral centers- the R and S system
  24. 4.5: Optical Activity
  25. 4.6: Compounds with multiple chiral centers
  26. 5: Overview of Organic Reactivity
  27. 5.0: Prelude to Organic Reactivity
  28. 5.1: A First Look at Some Organic Reaction Mechanism
  29. 5.2: A Quick Review of Thermodynamics and Kinetics
  30. 5.3: Catalysis
  31. 5.4: Comparing Biological Reactions to Laboratory Reactions
  32. 5.E: Overview of Organic Reactivity (Exercises)
  33. 5.S: Overview of Organic Reactivity (Summary)
  34. 6: Introduction to Reaction Mechanisms
  35. 6.0: Prelude to Radical Reactions
  36. 6.1: Overview of Single-Electron Reactions and Free Radicals
  37. 6.2: Prelude to Electrophilic Reactions
  38. 6.3: Electrophilic Addition to Alkenes
  39. 6.4: Stereochemistry of alkenes
  40. 6.5: Radical Chain Reactions
  41. 6.6: Useful Polymers formed by Radical Chain Reactions
  42. 6.7: Destruction of the Ozone Layer by a Radical Chain Reaction
  43. 7: Reaction Mechanisms Continued
  44. 7.0: Prelude to Nucleophilic Substitution Reactions
  45. 7.1: Two Mechanistic Models for Nucleophilic Substitution
  46. 7.2: Nucleophiles
  47. 7.3: Electrophiles
  48. 7.4: Leaving Groups
  49. 7.5: Prelude to Nucleophilic Carbonyl Addition Reactions
  50. 7.6: Nucleophilic Additions to Aldehydes and Ketones - An Overview
  51. 7.7: Hemiacetals, Hemiketals, and Hydrates
  52. 7.8: Acetals and Ketals
  53. 7.9: Prelude to Nucleophilic Acyl Substitution Reactions
  54. 7.10: Carboxylic Acid Derivatives
  55. 7.11: The Nucleophilic Acyl Substitution Mechanism
  56. 7.12: Hydrolysis of Thioesters, Esters, and Amides
  57. 8: Intro to Spectroscopy - UV-Vis, IR, MS
  58. 8.0: Prelude to Structure Determination I
  59. 8.1: Introduction to molecular spectroscopy
  60. 8.2: Mass Spectrometry
  61. 8.3: Infrared spectroscopy
  62. 8.4: Ultraviolet and visible spectroscopy
  63. 8.P: Problems for Chapter 4
  64. 9: Introduction to Acid-base Reactions
  65. 9.0: Prelude to Acid-base Reactions
  66. 9.1: Overview of Acid-Base Reactions
  67. 9.2: The Acidity Constant
  68. 9.3: Structural Effects on Acidity and Basicity
  69. 10: Introduction to Biomolecules
  70. 10.0: Introduction to Amino Acids and Proteins
  71. 10.1: Introduction to carbohydrate structure
  72. 10.2: Introduction to Lipid Structure
  73. 10.3: Introduction to nucleic acid (DNA and RNA) structure
  74. 10.4: Stereochemistry in biology and medicine
  75. Back Matter
  76. Index
  77. Glossary
  78. Detailed Licensing
  79. Detailed Licensing