1. You can recognize a reaction as an addition reaction based on the conversion of an alkene pi bond to two new bonds, one from each carbon, to a new atom or group.
  2. You recognize that in catalytic hydrogenation, the two atoms of H2 are delivered to the same face of the alkene: a syn addition.
  3. You can recognize how a chiral environment is needed (such as a chiral catalyst) in order to achieve enantioselective hydrogenation of an alkene.
  4. You can identify how an electrophile will interact with a pi bond in an alkene to generate a carbocation.
  5. If the electrophile is H+ (obviously, delivered by an appropriate conjugate base), you can predict which carbon of the alkene will accept the proton. You understand this as the mechanistic basis for the Markownikov rule.
  6. For H-X (H = Cl, Br, I, OH) you can predict the result of addition to any alkene.
  7. You recognize that carbocation rearrangements in H-X additions will behave as they do in E1 eliminations because of the involvement and properties of a carbocation.
  8. You can generalize the H-X addition mechanism to other species with polar or polarizable bonds: Cl-Cl, Br-Br, I-I, HOCl, HOBr, BrCl, ICl, BrCN, RS-Cl, HgX2/H2O.
    Visualization: Bromination of an alkene vs. an alkane (YouTube)
  9. You understand the participation of lone pairs in forming halonium ions, and the impact on stereospecificity when using X+ as an electrophile.
  10. You can apply the principles of electrophilic addition to the addition of B-H bonds to alkenes, and understand why we observe anti-Markownikov addition with these reagents.
  11. You understand the mechanism by which alkylboranes are converted to alcohols by hydrogen peroxide.
  12. You can use retrosynthetic thinking to see how to make either of two alcohols from an alkene, either by oxymercuration/demercuration, or by hydroboration/oxidation.
  13. You know that carbenes share electrophilic and nucleophilic character and can add to alkenes to form cyclopropanes. You understand the stereospecific outcome of these additions, based on alkene configuration.
  14. You know that peroxycarboxylic acids have the same shared electrophilic/nucleophilic character, and can add a single oxygen atom to an alkene to form an epoxide.
  15. You know that metal oxo reagents OsO4 and KMnO4 will react with an alkene in a syn fashion to form a 1,2-diol (a vicinal diol).
  16. You know that ozone (O3) will oxidatively cleave alkenes to give carbonyl compounds, and what structural features and elements of the workup lead to ketones, aldehydes or carboxylic acids.
  17. You understand radical addition to alkenes: in general, the formation of the more substituted alkyl radical, and specifically the formation of anti-Markownikov products in the addition of H-X or formation of polymers.

Recommended end-of-chapter problems: 12-39, 12-40, 12-41, 12-42, 12-44, 12-46, 12-47, 12-48, 12-49, 12-50, 12-53, 12-61, 12-67, 12-78.
Friday fun: Discovering the Mechanism of Osmylation