Reactions
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- 1133
- Reaction Fundamentals
- Addition Reactions
- Addition to Carbonyls
- Carbonyls are Electrophiles
- CO10. Activation of Carbonyls
- CO11. Addition of Neutral, Protic Nucleophiles
- CO12. Proton Transfer Steps
- CO13. \(\pi\) Donation Steps
- CO15. The Anomeric Center
- CO16. Biological Reduction
- CO17. Oxidation
- CO19. Conjugate Addition
- CO2. General Reactivity Patterns
- CO20. Conjugate Addition-Elimination in Aromatics
- CO21. Carbonyl Addition Summary: Mechanistic Steps
- CO23. Solutions to Selected Problems, CO1-9
- CO24. Solutions to Selected Problems, CO10-18
- CO3. MO Picture of Carbonyls
- CO4. Relative Reactivity of Carbonyls
- CO5. Nucleophilic Addition
- CO6. Protonation of Oxygen
- CO7. What is a Good Nucleophile?
- CO8. Semi-Anionic Nucleophiles
- CO9. Enolate Addition and Homologation
- Pyranose and Furanose Forms
- Ylide Addition
- Electrophilic Addition Reactions
- Nucleophilic Addition Reactions
- Addition to Carbonyls
- Reactivity
- Electrophilic Addition to Alkenes
- Electrophilic Aromatic Substitution
- Ligand Substitution in Coordination Complexes
- Nucleophilic Substitution at Tetrahedral Carbon
- NS1. Introduction to ANS
- NS10. Leaving Group Formation
- NS11. NA to Strained Rings
- NS12. Elimination Reactions
- NS13. Regiochem. in Elimination
- NS14. Stereochem in Elimination
- NS15. Elim. Mechanism Factors
- NS16. Solutions for Problems
- NS2. Possible Mechanisms of NS
- Rate Laws in Nucleophilic Substitution
- NS4. Stereochemistry in NS
- NS5. Regiochemistry in NS
- NS6. Structural Effects in NS
- NS7. Solvent Effects in NS
- NS8. Nucleophilicity in NS
- NS9. Enolate Nucleophiles
- Oxidative Addition & Reductive Elimination
- Part V: Reactivity in Organic, Biological and Inorganic Chemistry 3
- Roadmap Problems in Natural Product synthesis
- RR. Radical Reactions
- Reactivity of Alpha Hydrogens
- Elimination Reactions
- Substitution Reactions
- Carboxyl Substitution
- Comparative Energies: The Ski Hill
- CX11. Protein Modifications
- CX12. Solutions For Selected Problems
- CX2. General Reactivity Patterns
- CX5. Getting Towed Uphill
- CX6. Semi-Anionic Nucleophiles
- CX7. Enolates: Substitution and Decarboxylation
- CX8. Condensation Polymers
- CX9. Peptides and Proteins: Laboratory Synthesis
- Interconversion of Carboxyloids: Going Downhill
- Introduction to Carboxyloids (Acid Derivatives)
- Electrophilic Substitution Reactions
- IV. Nucleophilic Substitution Reactions
- Kinetics of Nucleophilic Substitution Reactions
- SN1
- SN2
- Carboxyl Substitution
- Rearrangement Reactions
- Free Radical Reactions
- Oxidation and Reduction Reactions
- Named Reactions
- Appel Reaction
- Baeyer-Villiger oxidation
- Bartoli indole synthesis
- Baylis-Hillman reaction
- Beckmann Rearrangement
- Biginelli reaction
- Birch Reduction
- Buchwald-Hartwig amination
- Cannizzaro reaction
- Chugaev Reaction
- Claisen rearrangement
- Cope Elimination
- Corey-Kim oxidation
- Curtius Rearrangement
- Dakin-West reaction
- Dakin Oxidation
- Dieckmann condensation
- Diels-Alder reaction
- Eschenmoser-Claisen rearrangement
- Eschweiler-Clarke reaction
- Finkelstein reaction
- Fischer esterification
- Fischer indole synthesis
- Friedel-Crafts acylation
- Friedel-Crafts alkylation
- Fries rearrangement
- Gabriel synthesis
- Grignard reaction
- Heck reaction
- Hell-Volhard-Zelinsky reaction
- Henry reaction
- Hofmann Elimination
- Hofmann rearrangement
- Horner-Wadsworth-Emmons Reaction
- Ireland-Claisen rearrangement
- Johnson-Claisen rearrangement
- Jones oxidation
- Knoevenagel condensation
- Knorr pyrazole synthesis
- Kolbe-Schmitt reaction
- Kumada cross-coupling
- Luche reduction
- Mannich reaction
- Michael addition
- Mitsunobu Macrolactonization
- Mitsunobu reaction
- Mukaiyama aldol addition
- Named Reagents
- Negishi cross-coupling
- Oppenauer oxidation
- Overman Rearrangement
- Pauson-Khand reaction
- Perkin reaction
- Pictet-Spengler reaction
- Prins reaction
- Pummerer Rearrangement
- Reformatsky reaction
- Reimer-Tiemann reaction
- Ritter reaction
- Robinson annulation
- Schmidt reaction
- Schotten-Baumann reaction
- Sharpless epoxidation
- Sonogashira cross-coupling
- Staudinger reaction
- Stille cross-coupling
- Strecker amino acid synthesis
- Suzuki cross-coupling
- Swern oxidation
- Tamao-Fleming Oxidation
- TES protection
- Ullmann reaction
- Vilsmeier-Haack reaction
- Wagner-Meerwein rearrangement
- Williamson ether synthesis
- Wittig reaction
- Wolff-Kishner reduction
- Wolff rearrangement
- Yamaguchi Esterification
- Organic Reactions
- Aldol Condensation
- Cannizzaro Reaction
- Claisen Condensation
- Claisen Rearrangement
- Clemmensen Reduction
- Dieckmann Condensation
- Formation of Cyclic Ketones by Intramolecular Acylation
- Hydroamination Reactions of Alkenes
- Jacobsen Rearrangement
- Mannich Reaction
- Periodic Acid Oxidation
- Preparation of Aliphatic Fluorine Compounds
- Preparation of Unsymmetrical Biaryls by the Diazo Reaction and the Nitrosoacetylamine Reaction
- Reduction with Aluminum Alkoxides (The Meerwein-Ponndorf-Verley Reduction)
- Replacement of the Aromatic Primary Amino Group by Hydrogen
- Schmidt Reaction
- Wacker Oxidation
- Wittig Reaction
- Pericyclic Reactions
- Zimmerman-Traxler Model
- Keck Asymmetric Allylation
- Chan Rearrangement
- Introduction to Bioconjugation
Organic Chemistry is fun since there are so many different types of reactions that can be done.