In the previous section, we saw that we can use electronegativity, induction, polarizability and resonance to understand and predict the relative stabilities of charged molecules. In this section, we will apply this knowledge to predict the relative strengths of acids and bases.
2.1: Alkane nomenclature
2.2: Alkene and alkyne nomenclature
2.3: Common names for branching substituents
2.4: Cyclic hydrocarbon nomenclature
2.5: Identifying functional groups
2.6: Naming low-priority functional groups (ethers, sulfides, and halides)
2.7: High priority functional groups
2.8: Common names