Cross-References

Estimated reading time: 1 min

Chapter 3 (Acids and Bases) — the conceptual framework (stability of the conjugate base) that this appendix supplies values for.
Chapter 8 (Elimination) — alkoxide and other strong, non-resonance-stabilized bases as the reagents that drive E2 elimination.
Chapter 9 (Addition) — terminal alkyne acidity and its use in alkylation chemistry.
Chapter 14 (Enols and Enolates) — the mechanism behind α-carbon acidity and enolate resonance in full detail.
Chapter 17 (Substituent Effects) — how ring substituents shift phenol and aniline acid/base strength.
Appendix A (Functional Group Atlas) — polarity and reactivity notes for each compound class referenced here.

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