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