Organic Chemistry-Part 1 Fundamentals

by Muhammad Arif Malik

Read here Read at LibreTextsPDF
Publisher
Hampton University
Subjects
Chemistry, Organic Chemistry
Licence
Public domain, as LibreTexts states it
Who can read
Tweens profiles and older, judged from its title and subjects

Contents

LibreTexts writes equations in TeX, and here they show as TeX; the PDF has them typeset.

  1. Front Matter
  2. TitlePage
  3. InfoPage
  4. Table of Contents
  5. Licensing
  6. 1: Bonding and structure
  7. 1.1: What is organic chemistry
  8. 1.2: Structure of an atom
  9. 1.3: Chemical bonds
  10. 1.4: Bonding theories and geometries of molecules
  11. 1.5: Polarity of bonds and molecules
  12. 2: Representing organic structures
  13. 2.1: Drawing organic structures
  14. 2.2: Resonance
  15. 2.3: Organic nomenclature -alkanes
  16. 2.4: Organic nomenclature -functional group containing compounds
  17. 3: Steriochemistry
  18. 3.1: Introduction to stereochemistry
  19. 3.2: Conformational analyses
  20. 3.3: Conformational analysis of cyclohexanes
  21. 3.4: Configurational stereoisomerism
  22. 3.5: Assigning R/S stereodescriptors to chirally center
  23. 3.6: Optical activity
  24. 3.7: Types of chiral molecules
  25. 3.8: Chirality related topics
  26. 4: Acids and bases
  27. 4.1: Importane of acids, bases and their reactions
  28. 4.2: Arrhenius Acids and Bases
  29. 4.3: Brønsted-Lowry Acids and Bases
  30. 4.4: Predicting the direction of acid-base reactions
  31. 4.5: Thermochemistry of acid-base reactions
  32. 4.6: Factors affecting the strength of an acid
  33. 4.7: Lewis acids and bases
  34. 5: Alkanes and radical reaction mechanisms
  35. 5.1: Physical propertes of alkanes
  36. 5.2: Chemical properties of alkanes
  37. 5.3: Terminologies related to reaciton mechanisms
  38. 5.4: Radical reaction mechanism -chlorination of methane
  39. 5.5: Selectivity in halogenation of alkanes
  40. 5.6: Autoxidation
  41. 6: Alkyl halides and Nucleophilic substitutions and elmiminations
  42. 6.1: Alkyl halides
  43. 6.2: Neuclophilic substitution bimolecular (SN2) reactions
  44. 6.3: E2 reactions
  45. 6.4: Nucleophilic substitution unimolecular (SN1) reactions
  46. 6.5: E1 reactions
  47. 6.6: Competition between SN2, E2, SN1, and E1 reactions
  48. Back Matter
  49. Index
  50. Glossary
  51. Detailed Licensing
  52. Detailed Licensing