The book dedicates significant space to cyclohexane, cyclopentane, and heterocycles (like tetrahydropyran). You will learn about axial vs. equatorial stability, the A-value (steric strain energy of substituents), and the anomeric effect in sugars.
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How do you assign R (Rectus) and S (Sinister) priority? The Cahn-Ingold-Prelog rules are explained with numerous examples, including tricky cases involving isotopes (e.g., deuterium vs. hydrogen). You will learn about specific rotation, enantiomeric excess (ee), and how to calculate optical purity. enantiomeric excess (ee)