Figures 1.10 and 1.11: Tetrahedral orbitals and the structure of methane

Figures 2.5 and 2.6: Lewis Acids and Lewis Bases

Chapter 3 Tutorial: IUPAC Nomenclature of Alkanes

Figure 4.5: The dihedral angle between methyl groups

Figure 4.21: Conformation of cis- and trans-1,2-dimethylcyclohexane

Figure 5.5: A reaction energy diagram

Figure 5.6: A hypothetical transition-state structure

Figure 6.14: Hypothetical transition state for alkene protonation

Figure 7.6: Mechanism of the hydroboration of 1-methylcyclopentene

Figure 8.6: The alkylation reaction of acetylide anion with bromomethane to give propyne

Figure 9.16: Stereochemistry of the addition of Br2 to cis-2-butene

Figure 9.17: Stereochemistry of the addition of Br2 to trans-2-butene

Figures 10.3 and 10.4: Various models of the allyl radical