Advance Organic Chemistry (UCI)

• 1.Nomenclature Bicyclic Compounds. (UCIRVINE)
• 2.Spirocyclic, Polycyclic, & Heterocyclic Compounds.(UCIRVINE)
• 3.Databases and the Chemical Literature.(UCIRVINE)
• 4.Stereochemistry Properties of Stereoisomers.(UCIRVINE)
• 5.Concepts in Stereochemistry.(UCIRVINE)
• 6.Stereoselectivity in the Aldol Reaction.(UCIRVINE)
• 7. Organic Reaction Mechanisms.(UCIRVINE)
• 8. Reaction Kinetics.(UCIRVINE)
• 9. Reaction Rates and the Eyring Equation.(UCIRVINE)
• 10. Linear Free-Energy Relationships.(UCIRVINE)
• 11. Molecular Orbitals and Aromaticity.(UCIRVINE)
• 13. Cycloadditions and Sigmatropic Rearrangements.(UCIRVINE)
• 14. Functional Group Transformation & Oxidation State.(UCIRVINE)
• 15. Oxidation & Reduction Alcohols & Carbonyl Compounds.(UCIRVINE)
• 16. Stereoselective Reduct.; Mitsunobu & Barton-Mc CombieRxns.(UCIRVINE)
• 17. The Carbonyl Group in Carbon-Carbon Bond Formation.(UCIRVINE)
• 18. Claisen Condensation and Michael Addition.(UCIRVINE)
• 19. Acid-Catalyzed Aldol Reactions and the Mannich Reaction.(UCIRVINE)
• 20. Enamines, the Wittig Reaction, and Cyclopropanation.(UCIRVINE)
• 21. Benzoin &Acyloin Condensations. Acyl Anion Equivalents.(UCIRVINE)
• 22. Retrosynthetic Analysis. Diels-Alder; Robinson Annulation.(UCIRVINE)
• 23. How Concentration, Stoichiometry, & Solvent Affect Rxns.(UCIRVINE)
• 24. How Temperature and Other Conditions Affect Reactions.(UCIRVINE)
• 25. NMR Spectroscopy How NMR Works. Chemical Shifts.(UCIRVINE)
• 26. Spin-Spin Coupling in 1H NMR Spectroscopy.(UCIRVINE)