| Chapitre 6 : The Reactions of Alkenes. The Stereochemistry of Addition Reactions |
Page |
| The Addition of a Hydrogen Halide to an Alkene |
236 |
| Carbocation Stability Depends on the Number of Alkyl Groups Attached to the Positively Charged Carbon |
237 |
| What Does the Structure of the Transition State Look Like? |
239 |
| Electrophilic Addition Reactions Are Regioselective |
241 |
| The Addition of Water to an Alkene |
245 |
| The Addition of an Alcohol to an Alkene |
246 |
| A Carbocation Will Rearrange if It Can Form a More Stable Carbocation |
248 |
| The Addition of Borane to an Alkene: Hydroboration–Oxidation |
250 |
| The Addition of a Halogen to an Alkene |
254 |
| The Addition of a Peroxyacid to an Alkene |
257 |
| The Addition of Ozone to an Alkene: Ozonolysis |
259 |
| Regioselective, Stereoselective, And Stereospecific Reactions |
263 |
| The Stereochemistry of Electrophilic Addition Reactions |
264 |
| The Stereochemistry of Enzyme-Catalyzed Reactions |
276 |
| Enantiomers Can Be Distinguished by Biological Molecules |
277 |
| Reactions and Synthesis |
278 |