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A free-radical reaction is any chemical reaction involving free radicals. This reaction type is abundant in organic reactions. Two pioneering studies into free radical reactions have been the discovery of the triphenylmethyl radical by Moses Gomberg (1900) and the lead-mirror experiment〔''Über die Darstellung von freiem Methyl'' Berichte der deutschen chemischen Gesellschaft (A and B Series) Volume 62, Issue 5 , Pages 1335–47 Fritz Paneth, Wilhelm Hofeditz 〕 described by Friedrich Paneth in 1927. In this last experiment tetramethyllead is decomposed at elevated temperatures to methyl radicals and elemental lead in a quartz tube. The gaseous methyl radicals are moved to another part of the chamber in a carrier gas where they react with lead in a mirror film which slowly disappears. When radical reactions are part of organic synthesis the radicals are often generated from radical initiators such as peroxides or azobis compounds. Many radical reactions are chain reactions with a chain initiation step, a chain propagation step and a chain termination step. Reaction inhibitors slow down a radical reaction and radical disproportionation is a competing reaction. Radical reactions occur frequently in the gas phase, are often initiated by light, are rarely acid or base catalyzed and are not dependent on polarity of the reaction medium.〔(Free Radical Reaction – from Eric Weisstein's World of Chemistry )〕 Reactions are also similar whether in the gas phase or solution phase. == Kinetics == The chemical kinetics of a radical reaction depend on all these individual reactions. In steady state the concentrations of initiating (I.) and terminating species T. are negligent and rate of initiation and rate of termination are equal. The overall reaction rate can be written as:〔''Advanced Organic Chemistry'' F.A. Carey R.J. Sundberg ISBN 0-306-41198-9〕 : with a broken-order dependence of 1.5 with respect to the initiating species. The reactivity of different compounds toward a certain radical is measured in so-called competition experiments. Compounds bearing carbon–hydrogen bonds react with radicals in the order primary < secondary < tertiary < benzyl < allyl reflecting the order in C–H bond dissociation energy〔 Many stabilizing effects can be explained as resonance effects, an effect specific to radicals is the captodative effect. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Free-radical reaction」の詳細全文を読む スポンサード リンク
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