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 |