Free-radical addition
Free-radical addition is an addition reaction in organic chemistry involving free radicals.[1] The addition may occur between a radical and a non-radical, or between two radicals.
The basic steps with examples of the free-radical addition (also known as radical chain mechanism) are:
- Initiation by a radical initiator: A radical is created from a non-radical precursor.
- Chain propagation: A radical reacts with a non-radical to produce a new radical species
- Chain termination: Two radicals react with each other to create a non-radical species
Free-radical reactions depend 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. An example of an addition reaction involving aryl radicals is the Meerwein arylation.
Contents
Addition of mineral acid to an alkene[edit]
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. Free-radical addition does not occur with the molecules HCl or HI. Both reactions are extremely endothermic and are not chemically favored.
Self-terminating oxidative radical cyclizations[edit]
In one specific type of radical addition called self-terminating oxidative radical cyclization, alkynes are oxidized to ketones with intramolecular radical cyclization 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.
See also[edit]
- The other radical reactions: radical substitution and radical polymerization.
References[edit]
- ^ 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
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