CH-2240 Lecture Notes - Lecture 12: Methyl Radical, Unpaired Electron, Bromine

• School: Clemson University
• Department: Chemistry
• Course: CH-2240
• Professor: Elliot Ennic

Document Summary

Chemistry atoms in an alkane has any significant charge. Chapter 12 radicals reactions of alkanes: alkanes saturated hydrocarbons (saturated with hydrocarbons no double. 12. 1 alkanes are unreactive compounds: electrons in ch and cc bonds are shared relatively equally none of the. 12. 3 radical stability depends on the number of alkyl groups attached to the. 12. 6 formation of explosive peroxides radical will remove h atom from tert carbon faster than a secondary carbon (and so on: bromination is a much slower reaction than chlorination selective about forming primary, secondary, tertiary radicals. Hcl or hi hydrogens (mark rule: peroxide a compound with an o-o bond, easily cleaved homolytically (forming radicals) radical initiator. 12. 7 the addition of radicals to an alkene: hbr added to an alkene br is added to carbon with greater number of, hbr added to alkene with peroxide anti mark rule.