Free-radical addition

In organic chemistry, free-radical addition is an addition reaction which involves free radicals. Radical additions are known for a variety of unsaturated substrates, both olefinic or aromatic and with or without heteroatoms.

Free-radical reactions depend on one or more relatively weak bonds in a reagent. Under reaction conditions (typically heat or light), some weak bonds homolyse into radicals, which then induce further decomposition in their compatriots before recombination. Different mechanisms typically apply to reagents without such a weak bond.

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Mechanism and regiochemistry

The basic steps in any free-radical process (the radical chain mechanism) divide into:^[1]

Radical initiation: 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

In a free-radical addition, there are two chain propagation steps. In one, the adding radical attaches to a multiply-bonded precursor to give a radical with lesser bond order. In the other, the newly-formed radical product abstracts another substituent from the adding reagent to regenerate the adding radical.^[2]^{: 743–744}

In general, the adding radical attacks the alkene at the most sterically accessible (typically, least substituted) carbon; the radical then stabilizes on the more substituted carbon.^[2]^{: 188, 751} The result is typically anti-Markovnikov addition, a phenomenon Morris Kharasch called the "peroxide effect".^[3] Reaction is slower with alkynes than alkenes.^[2]^: 750

In the paradigmatic example, hydrogen bromide radicalyzes to monatomic bromine. These bromine atoms add to an alkene at the most accessible site, to give a bromoalkyl radical, with the radical on the more substituted carbon. That radical then abstracts a hydrogen atom from another HBr molecule to regenerate the monatomic bromine and continue the reaction.^[2]^: 758

Compounds that add radically

Radical addition of hydrogen bromide is a valuable synthetic technique for anti-Markovnikov carbon substitution,^{[citation needed]} but free-radical addition does not occur with the other hydrohalic acids. Radical formation from HF, HCl, or HI is extremely endothermic and chemically disfavored.^[2]^{: 692–694} Hydrogen bromide is incredibly selective as a reagent,^[2]^{: 687–688} and does not produce detectable quantities of polymeric byproducts.^[4]^{: 156–157}

The behavior of hydrogen bromide generalizes in two separate directions. Halogenated compounds with a relatively stable radical can dissociate from the halogen. Thus, for example, sulfonyl, sulfenyl, and other sulfur halides can add radically to give respectively β‑halo sulfones, sulfoxides, or sulfides.^[4]^{: 200, 204, 206}

Separately, unsubsituted compounds with a relative stable radical can dissociate from hydrogen. In general, these reactions risk polymerized byproducts (see § Side reactions). For example, in the thiol-ene reaction, thiols,^[4]^{: 165–166} disulfides,^[4]^: 207 and hydrogen sulfide^[4]^: 191 add across a double bond. But if the unsaturated substrate polymerizes easily, they catalyze polymerization instead.^[4]^{: 171–172} In thermal silane additions, telomerization usually proceeds to about 6 units.^[4]^: 211

In the case of silicon, germanium, or phosphorus, the energetics are unfavorable unless the heavy atom bears a pendant hydrogen.^[4]^{: 209, 217–219} Other electronegative substituents on silicon appear to reduce the barrier.^[4]^{: 213, 217–224}

Although nitrogen oxides naturally radicalize, careful control of the radical species is difficult. Dinitrogen tetroxide adds to give a mixture: a vicinal dinitro compound, but also a nitro substituent adjacent to a nitrite ester.^[4]^: 225

To aryl radicals

Although aromatic resonance stabilizes aryl radicals, bonds between arenes and their substituents are (in)famously strong. Radical reactions with arenes typically present retrosynthetically as instances of nucleophilic aromatic substitution,^{[citation needed]} because generating the aryl radical requires a strong (radical) leaving group.^[2]^{: 686–687} One example is the Meerwein arylation.

Side reactions

A radical addition which leaves an unsaturated product can undergo radical cyclization between the two propagation steps.^[2]^: 744 In general, radical additions can also start radical polymerization processes.^[4]^{: 171–172}

With stable inorganic radicals

In self-terminating oxidative radical cyclization, inorganic radicals oxidize alkynes to ketones through an intramolecular radical cyclization. This reaction is not catalytic, and requires the oxidized radical source in stoichiometric amounts. In effect, the radical species is synthetically equivalent to monatomic oxygen.^[5]

In the paradigmatic example, a nitrate radical (from photolysis of ceric ammonium nitrate) adds to an alkyne to generate a very reactive vinyl nitrate ester radical. The vinyl radical abstracts an intramolecular hydrogen atom 5 atoms away before 5-exo-trig ring-closure. The resulting alkyl nitrate radical can then fragment to a ketone and the stable radical nitrogen dioxide.^[5]

Sulfate (from ammonium persulfate) and hydroxyl radicals show similar reactivity.^[5]

References

^ L.G. Wade's Organic Chemistry 5th Ed. (p 319) – Mechanism supplements original.
^ ^a ^b ^c ^d ^e ^f ^g ^h March, Jerry (1992), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (4th ed.), New York: Wiley, ISBN 0-471-60180-2
^ Kharasch, M. S.; Mayo, Frank R. (1933). "The Peroxide Effect in the Addition of Reagents to Unsaturated Compounds. I. The Addition of Hydrogen Bromide to Allyl Bromide". Journal of the American Chemical Society. 55 (6): 2468–2496. doi:10.1021/ja01333a041.
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j ^k Stacey, F. W.; Harris, J. F., Jr. (30 April 2004). "Formation of carbon-hetero atom bonds by free-radical chain additions to carbon-carbon multiple bonds". In Denmark, Scott E. (ed.). Organic Reactions (1 ed.). Wiley. doi:10.1002/0471264180.or013.04. ISBN 978-0-471-26418-7.
^ ^a ^b ^c Dreessen, Tim; Jargstorff, Christian; Lietzau, Lars; Plath, Christian; Stademann, Arne; and Wille, Uta (2004). "Self-Terminating, Oxidative Radical Cyclizations". Molecules, issue 9, pp. 480–497.

v t e Basic reaction mechanisms
Nucleophilic substitutions	Unimolecular nucleophilic substitution (S_N1) Bimolecular nucleophilic substitution (S_N2) Nucleophilic aromatic substitution (S_NAr) Nucleophilic internal substitution (S_Ni) Nucleophilic acyl substitution (S_NAcyl)
Electrophilic substitutions	Electrophilic aromatic substitution (S_EAr)
Elimination reactions	Unimolecular elimination (E1) E1cB-elimination Bimolecular elimination (E2) E_i elimination
Addition reactions	Electrophilic addition Nucleophilic addition Free-radical addition Cycloaddition Oxidative addition
Unimolecular reactions	Intramolecular reaction Isomerization Photodissociation Lindemann–Hinshelwood mechanism RRKM theory
Electron/Proton transfer reactions	Redox Harpoon reaction Grotthuss mechanism Marcus theory Inner sphere electron transfer Outer sphere electron transfer
Medium effects	Solvent effects Cage effect Matrix isolation
Related topics	Elementary reaction Reaction dynamics Reactive intermediate Radical (chemistry) Molecularity Stereochemistry Catalysis Collision theory Arrow pushing Potential energy surface More O'Ferrall–Jencks plot
Chemical kinetics	Rate equation Equilibrium constant Rate-determining step Reaction coordinate Energy profile (chemistry) Transition state theory Activation energy Activated complex Arrhenius equation Eyring equation Michaelis–Menten kinetics Diffusion-controlled reaction

This page was last edited on 4 April 2024, at 00:59

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