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When a radical adds across the π bond of an alkene, it generates a new radical at a carbon center. For example, a bromine radical interacting with an alkene produces a carbon-centered radical. This process dissolves the π bond while preserving the unpaired electron, following spin conservation principles similar to charge conservation in chemical reactions.

Spin conservation in radical reactions parallels charge conservation in traditional chemistry. A reactant with an unpaired electron must form a product with an unpaired electron. This fundamental principle ensures that when a radical adds to a spin-paired molecule, the resulting product retains an unpaired electron, maintaining the total spin state throughout the reaction.

Birch reduction is a radical formation process where group 1 metals dissolve in liquid ammonia to generate electrons. These electrons react with ketones to form ketyl radicals, which are stable radical intermediates. This represents the simplest category of radical formation via addition, where a single electron is added to a spin-paired molecule.

Radical addition functions as reduction because a single electron is added to a spin-paired molecule. In processes like Birch reduction, metals generate electrons that add to unsaturated species such as ketones. This electron addition converts the spin-paired molecule into a radical species, making it the most facile category of radical formation through addition mechanisms.

Group 1 metals dissolve in liquid ammonia to produce electrons that initiate radical formation. These electrons add to unsaturated organic compounds, generating radical intermediates. The metal is oxidized to a stable M+1 ion during this process, making it an effective electron source for radical addition reactions in synthetic organic chemistry.

Radical addition involves unpaired electrons and follows spin conservation rather than charge-driven mechanisms. When a radical adds to an alkene's π bond, it produces a new radical at a carbon center. Unlike ionic additions, radical additions preserve unpaired electrons throughout the reaction and do not rely on carbocation intermediates or charge stabilization.

Unsaturated species with π bonds readily undergo radical addition. Alkenes are common substrates where radicals like bromine add across the double bond to form carbon-centered radicals. Ketones also participate in radical addition, particularly in reduction processes like Birch reduction, where electrons add to the carbonyl π bond to generate ketyl radicals.