1. Acknowledgments ,
2. Structure and properties ,
3. Methane Energy of activation. Transition state ,
4. Alkanes Free-radical substitution ,
5. Stereochemistry I. Stereoisomers ,
6. Alkyl halides Nucleophilic aliphatic substitution ,
7. Alcohol and ethers ,
8. Role of the solvent Secondary bonding ,
9. Alkenes I. Structure and preparation Elimination ,
10. Alkenes II. Reactions of the carbon-carbon double bond electrophilic and free-radical addition ,
11. Stereochemistry II. Stereoselective and stereopecific reactions ,
12. Conjugation and resonance Dienes ,
13. Alkynes ,
14. Cyclic aliphatic compounds ,
15. Aromaticity Benzene ,
16. Electrophilic aromatic substitution ,
17. Aromatic-aliphatic compounds Arenes and their derivatives ,
18. Spectroscopy and structure ,
19. Aldehydes and ketones Nucleophilic addition ,
20. Carboxylic acids ,
21. Functional derivatives of carboxylic acids Nucleophilic acyl substitution ,
22. Carbanions I Aldol and claisen condensations ,
23. Amines I. Preparation and physical properties ,
24. Amines II. Reactions ,
25. Phenols ,
26. Carbanions I Malonic ester and acetoacetic ester syntheses ,
27. Aryl halides Nucleophilic aromatic substitution ,
28. ,-unsaturated carbonyl compounds Conjugate addition ,
29. Molecular orbitals. Orbital symmetry ,
30. Symphoria Neighboring group effects. Catalysis by transition metal complexes ,
31. Heterocyclic compounds ,
32. Macromolecules. Polymers and polymerization ,
33. Stereochemistry III. Enantiotopic and diastereotopic ligands ,
34. Lipids Fats and steroids ,
35. Carbohydrates I. Monosaccharides ,
36. Carbohydrates II. Disaccharides and polysaccharides ,
37. Proteins and nucleic acids Molecular biology.