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Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired molecule. These three possible reactions result in six different arrow-pushing patterns in radical mechanisms, such as homolysis, addition to a π bond, hydrogen abstraction, halogen abstraction, elimination, and coupling. These six patterns can be categorized into three typical steps, initiation, propagation, and termination, of a radical mechanism. Typically, these radical reactions are governed by two key factors: steric hindrance and electronic stabilization.

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RadicalsRadical ReactionsRadical radical CouplingSpin paired MoleculeRadical DecompositionUnimolecular ReactionArrow pushing PatternsHomolysisHydrogen AbstractionHalogen AbstractionEliminationInitiationPropagationTerminationSteric HindranceElectronic Stabilization

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20.8 : Radical Reactivity: Overview

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20.1 : Radicales: Estructura Electrónica y Geometría

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20.2 : Espectroscopía de Resonancia Paramagnética Electrónica (EPR): Radicales Orgánicos

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20.3 : Formación Radical: Visión General

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20.4 : Formación de radicales: homólisis

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20.5 : Formación Radical: Abstracción

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20.6 : Formación de radicales: Adición

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20.7 : Formación de Radicales: Eliminación

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20.9 : Reactividad radical: efectos estéricos

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20.10 : Reactividad de radicales: efectos de concentración

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20.11 : Reactividad de radicales: radicales electrofílicos

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20.12 : Reactividad de radicales: radicales nucleofílicos

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20.13 : Reactividad de radicales: intramolecular vs intermolecular

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20.14 : Autoxidación radical

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20.15 : Oxidación radical de alcoholes alílicos y bencílicos

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