Structure, Bonding, and Reactivity of Alkenes
- Page ID
- 23379
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- Chapter 11: Alkenes-Infrared and Mass Spectroscopy
- Section 11.1: Nomenclature of Alkenes
- Section 11.2: Structure and Bonding in Ethene-The π Bond
- Section 11.3: Physical Properties of Alkenes
- Section 11.4: Nuclear Magnetic Resonance (NMR) of Alkenes
- Section 11.5: Infared Spectroscopy
- Section 11.6: Measuring the Molecular Mass of Organic Compounds-Mass Spectroscopy
- Section 11.7: Fragmentation Patterns of Organic Molecules
- Section 11.8: Degree of Unsaturation
- Section 11.9: Catalytic Hydrogenation of Alkenes-Relative Stability of Double Bonds
- Section 11.10: Preparation of Alkenes from Haloalkanes and Alkyl Sulfonates-Bimolecular Elimination Revisited
- Section 11.11: Preparation of Alkenes by Dehydration of Alcohols
- Chapter 12: Reactions of Alkenes
- Section 12.2: Catalytic Hydrogenation
- Section 12.3: Nucleophilic Character of the ? Bond-Electrophilic Addition of Hydrogen Halides
- Section 12.4: Alcohol Synthesis by Electrophilic Hydration
- Section 12.5: Electrophilic Addition of Halogens to Alkenes
- Section 12.6: The Generality of Electrophilic Addition
- Section 12.7: Oxymercuration Demercuration-A Special Electrophilic Addition
- Section 12.8: Hydroboration Oxidation-A Stereospecific Anti-Markovnikov Hydration
- Section 12.9: Diazomethane, Carbenes, and Cyclopropane Synthesis
- Section 12.10: Oxacyclopropane (Epoxide) Synthesis- Epoxidation by Peroxycarboxylic Acids
- Section 12.11: Vicinal Syn Dihydroxylation with Osmium Tetroxide
- Section 12.12: Ozonolysis
- Section 12.13: Radical Additions--Anti-Markovnikov Product Formation
- Section 12.14: Dimerization, Oligomerization, and Polymerization of Alkenes
- Section 12.15: Polymerization