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  2. Free-radical reaction - Wikipedia

    en.wikipedia.org/wiki/Free-radical_reaction

    A free-radical reaction is any chemical reaction involving free radicals. This reaction type is abundant in organic reactions . Two pioneering studies into free radical reactions have been the discovery of the triphenylmethyl radical by Moses Gomberg (1900) and the lead-mirror experiment [ 1 ] described by Friedrich Paneth in 1927.

  3. Radical substitution - Wikipedia

    en.wikipedia.org/wiki/Radical_substitution

    In organic chemistry, a radical-substitution reaction is a substitution reaction involving free radicals as a reactive intermediate. [1] The reaction always involves at least two steps, and possibly a third. In the first step called initiation (2,3), a free radical is created by homolysis.

  4. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...

  5. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    Free-radical intermediate is stabilized by hyperconjugation; adjacent occupied sigma C–H orbitals donate into the electron-deficient radical orbital. A new method of anti-Markovnikov addition has been described by Hamilton and Nicewicz, who utilize aromatic molecules and light energy from a low-energy diode to turn the alkene into a cation ...

  6. Neighbouring group participation - Wikipedia

    en.wikipedia.org/wiki/Neighbouring_group...

    In this type of substitution reaction, one group of the substrate participates initially in the reaction and thereby affects the reaction. A classic example of NGP is the reaction of a sulfur or nitrogen mustard with a nucleophile, the rate of reaction is much higher for the sulfur mustard and a nucleophile than it would be for a primary or secondary alkyl chloride without a heteroatom.

  7. Category:Free radical reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Free_radical...

    Pages in category "Free radical reactions" ... Radical substitution; Radical-nucleophilic aromatic substitution; Reversible-deactivation radical polymerization; S.

  8. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    In the third type of substitution reaction, radical substitution, the attacking particle is a radical. [44] This process usually takes the form of a chain reaction, for example in the reaction of alkanes with halogens. In the first step, light or heat disintegrates the halogen-containing molecules producing radicals.

  9. Free radical substitution - Wikipedia

    en.wikipedia.org/?title=Free_radical...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Free_radical_substitution&oldid=44200152"https://en.wikipedia.org/w/index.php?title=Free_radical_substitution