Freshman Organic Chemistry II with Michael McBride - 12. Nucleophilic Participation During Electrophilic Addition to Alkenes

Freshman Organic Chemistry II (CHEM 125B) When electrophilic addition involves a localized carbocation intermediate, skeletal rearrangement sometimes occurs, but it can be avoided when both alkene carbons are involved in an unsymmetrical 3-center-2-electron bond, as in Markovnikov hydration via alkoxymercuration followed by reduction. Similarly a reagent that attacks both alkene carbons simultaneously by providing a nucleophilic component during electrophilic attack can avoid rearrangement, as in reactions that proceed via three-membered-ring halonium intermediates. Simultaneity in making two bonds during formation of cyclopropanes from carbenes can be demonstrated using stereochemistry. Anti-Markovnikov hydration can be achieved via hydroboration followed by oxidation with hydroperoxide. Rearrangement of the borane hydroperoxide intermediate with frontside C-O bond formation shows close orbital analogy to backside attack during SN2 substitution. Again syn-addition shows that nucleophilic attack occurs simultaneously with electrophilic attack on the alkene. 00:00 - Chapter 1. Forming Unrearranged Alcohols via Hydroxymercuration 07:36 - Chapter 2. Electrophilic Addition to Alkenes with Nucleophilic Participation: Halonium Ions 24:56 - Chapter 3. Electrophilic Addition to Alkenes with Nucleophilic Participation: Carbenes 36:55 - Chapter 4. Anti-Markovnikov Hydration via Hydroboration and Oxidation Complete course materials are available at the Open Yale Courses website: http://oyc.yale.edu This course was recorded in Spring 2011.