| Chapitre 8 : Delocalized Electrons: Their Effect on Stability, pKA, and the Products of a Reaction. Aromaticity and Electronic Effects: An Introduction to the Reactions of Benzene |
Page |
| Delocalized Electrons Explain Benzene's Structure |
319 |
| The Bonding in Benzene |
321 |
| Resonance Contributors and the Resonance Hybrid |
322 |
| How to Draw Resonance Contributors |
323 |
| The Predicted Stabilities of Resonance Contributors |
326 |
| Delocalization Energy is the Additional Stability Delocalized Electrons Give to a Compound |
329 |
| Delocalized Electrons Increase Stability |
330 |
| A Molecular Orbital Description of Stability |
335 |
| Delocalized Electrons Affect pKA Values |
339 |
| Electronic Effects |
342 |
| Delocalized Electrons Can Affect the Product of a Reaction |
346 |
| Reactions of Dienes |
347 |
| Thermodynamic Versus Kinetic Control |
350 |
| The Diels–Alder Reaction is a 1,4-Addition Reaction |
355 |
| Retrosynthetic Analysis of the Diels–Alder Reaction |
361 |
| Benzene is an Aromatic Compound |
362 |
| The Two Criteria for Aromaticity |
363 |
| Applying the Criteria for Aromaticity |
364 |
| A Molecular Orbital Description of Aromaticity |
367 |
| Aromatic Heterocyclic Compounds |
368 |
| How Benzene Reacts |
370 |