Addition Reactions Last updated Save as PDF Page ID1134 Addition to CarbonylsCarbonyls are ElectrophilesCO10. Activation of CarbonylsCO11. Addition of Neutral, Protic NucleophilesCO12. Proton Transfer StepsCO13. \(\pi\) Donation StepsCO15. The Anomeric CenterCO16. Biological ReductionCO17. OxidationCO19. Conjugate AdditionCO2. General Reactivity PatternsCO20. Conjugate Addition-Elimination in AromaticsCO21. Carbonyl Addition Summary: Mechanistic StepsCO23. Solutions to Selected Problems, CO1-9CO24. Solutions to Selected Problems, CO10-18CO3. MO Picture of CarbonylsCO4. Relative Reactivity of CarbonylsCO5. Nucleophilic AdditionCO6. Protonation of OxygenCO7. What is a Good Nucleophile?CO8. Semi-Anionic NucleophilesCO9. Enolate Addition and HomologationPyranose and Furanose FormsYlide AdditionElectrophilic Addition ReactionsReactions of Alkenes with BromineReactions of Alkenes with Hydrogen HalidesReactions of Alkenes with Sulfuric AcidThe Generalized Electrophilic AdditionWhat is Electrophilic Addition?Nucleophilic Addition ReactionsThe Addition of Hydrogen Cyanide to Aldehydes and KetonesThe Reduction of Aldehydes and Ketones Topic hierarchy
