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- Complex and simple lipids, main classes of hydrolysable lipids, hydrolysis reactions with mechanism.
- Fatty acids: functional groups and reactivity.
- Structure of triglycerides: functional groups and reactivity, comments on biodiesel preparation methods.
- Absolute and relative configuration, drawing and assigning stereochemistry to D-alanine and S-serine.
- Reducing and non-reducing sugars: formation of glycosides.
- Anomers of monosaccharides, definition and discussion of mutarotation in glucose.
- α and β-glycosidic linkages in polysaccharides: drawing and comparing structures of amylose and cellulose.
- Amino acids with examples of secondary alcohol, amide, thiol, sulfide, phenol, side chain primary ammonium, side chain carboxylate, secondary amine.
- Nitrogen protecting groups in peptide synthesis: main protecting reactions (with mechanism).
- Carboxylic acid protecting groups in peptide synthesis: main protecting reactions (with mechanism).
- Protecting groups: orthogonal and modulated liability strategies with examples.
- Molar concentration calculation of a molecule dissolved in water using UV absorbance data.
- Description of the 1H-NMR spectrum of cinnamic acid, assigning all resonances considering chemical shift, multiplicity (with diagram), and integral.
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