Aldehydes and Ketones
- Page ID
- 23383
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- Chapter 17: Aldehydes and Ketones-The Carbonyl Group
- Section 17.1: Naming Aldehydes and Ketones
- Section 17.2: The Carbonyl Group
- Section 17.3: Spectroscopic Properties of Aldehydes and Ketones
- Section 17.4: Preparation of Aldehydes and Ketones
- Section 17.5: Reactivity of the Carbonyl Group-Mechanisms of Addition
- Section 17.6: Addition of Water to Form Hydrates
- Section 17.7: Hemiacetals and Acetals
- Section 17.8: Acetals as Protecting Groups
- Section 17.9: Nucleophilic Addition of Ammonia and Its Derivatives
- Section 17.10: Deoxygenation of the Carbonyl Group
- Section 17.11: Cyanohydrins
- Section 17.12: Addition of Phosphorus Ylides-The Wittig Reaction
- Section 17.13: Oxidation of Peroxycarboxylic Acids-The Baeyer Villager Oxidation
- Section 17.14: Oxidative Chemical Tests for Aldehydes
- Chapter 18: Enols, Enolates, and Aldol Condensation-Alpha, Beta Unsaturated Aldehydes and Ketones
- Section 18.1: Acidity of Aldehydes and Ketones-Enolate Ions
- Section 18.2: Keto-Enol Equilibria
- Section 18.3: Halogenation of Aldehydes and Ketones
- Section 18.4: Alkylation of Aldehydes and Ketones
- Section 18.5: Attack by Enolates on the Carbonyl Function-Aldol Condensation
- Section 18.6: Crossed Aldol Condensation
- Section 18.7: Intramolecular Aldol Condensation
- Section 18.8: Properties of ?, ?-Unsaturated Aldehydes and Ketones
- Section 18.9: Conjugate Additions to ?, ?-Unsaturated Aldehydes and Ketones
- Section 18.10: 1,2- and 1,4-Additions of Organometallic Reagents
- Section 18.11: Conjugate Additions of Enolate Ions-Michael Addition and Robinson Annulatiom