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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
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