厦门大学化学化工学院：《有机化学》课程教学资源（课件讲稿，双语版）第五章 烯烃 Alkenes 5.1 烯烃的结构 Structure of Alkenes 5.2 烯烃的命名 Nomenclature of Alkenes

厦门大学化学化工学院：《有机化学》课程教学资源（课件讲稿，双语版）第六章 炔烃和共轭二烯 Alkynes and Conjugated Dienes 6.2 炔烃的化学性质 Chemical Properties of Alkynes 6.3 炔烃的制备 Preparation of Alkynes

厦门大学化学化工学院：《有机化学》课程教学资源（课件讲稿，双语版）第七章 芳香烃 7.5 多环芳烃 Polycyclic Aromatic Hydrocarbons 7.6 非苯芳烃 Non-benzenoid Aromatics 7.7 碳笼（Fullerene）

9.3 醛酮的反应 Reactions of Aldehydes and Ketones

10.1A Production of Radicals 10.2A Homolytic Bond Dissociation Energies and Heats of Reaction

11.15A Ethers by Intermolecular Dehydration of Alcohols

Acid-Catalyzed hydration of Alkenes Oxymercuration-Demeruration Hydroboration-Oxidation

No addition of bromine No oxidation No hydroation Slow addition at high temperature and pressure

Many other pairs of reagents that form cabocations (orcarbocationlike species) may be used as well

The aldols formed in aldol additions can be easily dehydrated to yield conjugated enals (enones)