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  2. tert-Butyl peroxybenzoate - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_peroxybenzoate

    tert-Butyl peroxybenzoate (TBPB) an organic compound with the formula C 6 H 5 CO 3 CMe 3 (Me = CH 3). It is the most widely produced perester ; it is an ester of peroxybenzoic acid ( C 6 H 5 CO 3 H ).

  3. C11H14O3 - Wikipedia

    en.wikipedia.org/wiki/C11H14O3

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  4. Peroxybenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Peroxybenzoic_acid

    Peroxybenzoic acid is an organic compound with the formula C 6 H 5 CO 3 H. It is the simplest aryl peroxy acid.It may be synthesized from benzoic acid and hydrogen peroxide, [3] or by the treatment of benzoyl peroxide with sodium methoxide, followed by acidification.

  5. tert-Butyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_hydroperoxide

    tert-butyl hydroperoxide is potentially dangerous, but explosions are rare. [3]A solution of tert-butyl hydroperoxide and water with a concentration of greater than 90% is forbidden to be shipped according to US Department of Transportation Hazardous Materials Table 49 CFR 172.101.

  6. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    The general structure of an organic peroxide. In organic chemistry, organic peroxides are organic compounds containing the peroxide functional group (R−O−O−R′).If the R′ is hydrogen, the compounds are called hydroperoxides, which are discussed in that article.

  7. Kharasch–Sosnovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Kharasch–Sosnovsky_reaction

    The Kharasch–Sosnovsky reaction is a method that involves using a copper or cobalt salt as a catalyst to oxidize olefins at the allylic position, subsequently condensing a peroxy ester (e.g. tert-Butyl peroxybenzoate) or a peroxide resulting in the formation of allylic benzoates or alcohols via radical oxidation. [1]

  8. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    The benzoyl functional group.. In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen.

  9. Radical initiator - Wikipedia

    en.wikipedia.org/wiki/Radical_initiator

    In chemistry, radical initiators are substances that can produce radical species under mild conditions and promote radical reactions. [1] These substances generally possess weak bonds—bonds that have small bond dissociation energies.