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Oregon Institute of Technology: CHE 331 Organic Chemistry I

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Oregon Institute of Technology: CHE 331 Organic Chemistry I

Chemistry
Author
Travis Lund
Publisher
Oregon Institute of Technology
Source
LibreTexts
License
CC BY-NC-SA
Language
EN
Category
Basic Sciences
Read online Download PDF (open licence)
Contents· 69 sections
  1. 01: General Chemistry Recap
  2. 1.00: Prelude to Atoms Electron Configurations and Lewis Structures
  3. 1.01: Drawing Organic Structures
  4. 1.02: Valence Bond Theory
  5. 02: Functional Groups
  6. 2.00: Functional groups and organic nomenclature
  7. 2.01: Prelude to Organic Structure and Bonding II
  8. 03: Properties and Principles
  9. 3.00: Non-covalent interactions
  10. 3.01: Physical properties of organic compounds
  11. 3.02: Resonance
  12. 3.03: Molecular orbital theory- conjugation and aromaticity
  13. 04: Conformations and Stereochemistry
  14. 4.00: Prelude to Conformations and Stereochemistry
  15. 4.01: Conformations of open-chain organic molecules
  16. 4.02: Conformations of cyclic organic molecules
  17. 4.03: Chirality and stereoisomers
  18. 4.04: Naming chiral centers- the R and S system
  19. 4.05: Optical Activity
  20. 4.06: Compounds with multiple chiral centers
  21. 05: Overview of Organic Reactivity
  22. 5.00: Prelude to Organic Reactivity
  23. 5.01: A First Look at Some Organic Reaction Mechanism
  24. 5.02: A Quick Review of Thermodynamics and Kinetics
  25. 5.03: Catalysis
  26. 5.04: Comparing Biological Reactions to Laboratory Reactions
  27. 5.E: Overview of Organic Reactivity (Exercises)
  28. 5.S: Overview of Organic Reactivity (Summary)
  29. 06: Introduction to Reaction Mechanisms
  30. 6.00: Prelude to Radical Reactions
  31. 6.01: Overview of Single-Electron Reactions and Free Radicals
  32. 6.02: Prelude to Electrophilic Reactions
  33. 6.03: Electrophilic Addition to Alkenes
  34. 6.04: Stereochemistry of alkenes
  35. 6.05: Radical Chain Reactions
  36. 6.06: Useful Polymers formed by Radical Chain Reactions
  37. 6.07: Destruction of the Ozone Layer by a Radical Chain Reaction
  38. 07: Reaction Mechanisms Continued
  39. 7.00: Prelude to Nucleophilic Substitution Reactions
  40. 7.01: Two Mechanistic Models for Nucleophilic Substitution
  41. 7.02: Nucleophiles
  42. 7.03: Electrophiles
  43. 7.04: Leaving Groups
  44. 7.05: Prelude to Nucleophilic Carbonyl Addition Reactions
  45. 7.06: Nucleophilic Additions to Aldehydes and Ketones - An Overview
  46. 7.07: Hemiacetals Hemiketals and Hydrates
  47. 7.08: Acetals and Ketals
  48. 7.09: Prelude to Nucleophilic Acyl Substitution Reactions
  49. 7.10: Carboxylic Acid Derivatives
  50. 7.11: The Nucleophilic Acyl Substitution Mechanism
  51. 7.12: Hydrolysis of Thioesters Esters and Amides
  52. 08: Intro to Spectroscopy - UV-Vis, IR, MS
  53. 8.00: Prelude to Structure Determination I
  54. 8.01: Introduction to molecular spectroscopy
  55. 8.02: Mass Spectrometry
  56. 8.03: Infrared spectroscopy
  57. 8.04: Ultraviolet and visible spectroscopy
  58. 8.P: Problems for Chapter 4
  59. 09: Introduction to Acid-base Reactions
  60. 9.00: Prelude to Acid-base Reactions
  61. 9.01: Overview of Acid-Base Reactions
  62. 9.02: The Acidity Constant
  63. 9.03: Structural Effects on Acidity and Basicity
  64. 10: Introduction to Biomolecules
  65. 10.00: Introduction to Amino Acids and Proteins
  66. 10.01: Introduction to carbohydrate structure
  67. 10.02: Introduction to Lipid Structure
  68. 10.03: Introduction to nucleic acid (DNA and RNA) structure
  69. 10.04: Stereochemistry in biology and medicine