Free radical addition
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Free radical addition is an addition reaction in organic chemistry involving free radicals [1].
The basic steps with examples are:
Free radical addition depends on a reagent having a (relatively) weak bond, allowing it to homolyse to form radicals (often with heat or light). Reagents without such a weak bond would likely proceed via a different mechanism.
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[edit] Addition of mineral acid to an alkene
To illustrate, consider the alkoxy radical-catalyzed, anti-Markovnikov reaction of hydrogen bromide to an alkene. In this reaction, a catalytic amount of organic peroxide is needed to abstract the acidic proton from HBr and generate the bromine radical, however a full molar equivalent of alkene and acid is required for completion.
Note that the radical will be on the more substituted carbon.
[edit] Self-terminating oxidative radical cyclizations
In one specific type of radical addition called self-terminating oxidative radical cyclization, alkynes are oxidized to ketones with intramolecular ring closure and the radical species are inorganic rather than carbon based. This type of reaction is self-terminating because propagating is not possible and the initiator is used in stoichiometric amounts. [2].
As an example a nitrate radical is generated by photolysis of CAN which reacts with an alkyne to generate first a very reactive vinyl radical and then via a 1,5-hydrogen atom transfer (HAT) and 5-exo-trig ring-closure a ketyl radical. The ketyl dislodges a nitrite radical which is not reactive enough for propagation and the ketone is formed.
The radical species in effect is a single oxygen atom synthon. Other inorganic radical that show this type of reactivity are sulfate radical ions (from ammonium persulfate) and hydroxyl radicals.
[edit] Special Notes
Free radical addition does not occur with the molecules HCl or HI. Both reactions are extremely endothermic and are not chemically favored.
[edit] See also
The other radical reactions: radical substitution and radical polymerization.
[edit] References
- ^ L.G. Wade's Organic Chemistry 5th Ed. (p 319) - Mechanism supplements original.
- ^ Self-Terminating, Oxidative Radical Cyclizations Tim Dreessen, Christian Jargstorff, Lars Lietzau, Christian Plath, Arne Stademann and Uta Wille Molecules 2004, 9, 480–497 Online article
