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Resonance energy alkyl free radicals

The reaction requires only very small activation energies, and, so, can even be used to start free radical polymerizations at —100°C. The alkyl free radicals produced are particularly poorly resonance stabilized, and so, can undergo a series of side reactions, for example, transfer reactions. [Pg.205]

The rapidity of the reaction can be seen by the large effect low pressures ( 1 torr) of oxygen can have on the free radical polymerization of a reactive olefin such as styrene [22]. The reaction rate coefficients are expected to be typical for exothermic radical—radical reactions with essentially no activation energy. Thus, if R is alkyl, log(feQ/l mole-1 s-1) would be 9.0 0.5, and be independent of temperature. For simple resonance-stabilized radicals, log(feD/l mole-1 s-1) would be 8.5 0.5. [Pg.25]


See other pages where Resonance energy alkyl free radicals is mentioned: [Pg.103]    [Pg.277]    [Pg.91]    [Pg.71]    [Pg.466]    [Pg.240]    [Pg.365]    [Pg.209]    [Pg.164]    [Pg.62]    [Pg.266]    [Pg.62]    [Pg.911]    [Pg.181]   
See also in sourсe #XX -- [ Pg.217 ]

See also in sourсe #XX -- [ Pg.217 ]




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Alkyl radicals

Energy resonant

Free radicals resonance

Free-radicals alkylation

Radical alkylation

Resonance energy

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