Acids and Bases
Start with the big picture
The lesson begins with how σ and π bonds form and how hybridization affects geometry and bond properties. It then considers Lewis structures, formal charge, resonance, conjugation, and aromaticity as tools for understanding electron distribution and stability. Acid–base concepts include proton donors and acceptors, electron-pair donors and acceptors, conjugate pairs, and the relationship between Ka and pKa. The topic also surveys structural influences on acidity and basicity, including electronegativity, resonance, inductive effects, s-character, and anion size. Examples of organic acid and base classes and the role of solvent are included, alongside the Henderson–Hasselbalch equation and trends used to assess acid–base reaction direction.
What you'll learn
- Distinguish σ and π bonds by how their orbitals overlap.
- Relate hybridization and s-character to bond properties and acidity.
- Use resonance, formal charge, and conjugate-pair stability to compare acids and bases.
- Interpret Ka and pKa when assessing acid strength and reaction direction.
- Identify structural and solvent factors that influence acidity and basicity.
Continue your study
Work through the complete notes and reinforce the topic with the study tools available in the full lesson.