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  2. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    Together with its conjugate base superoxide, hydroperoxyl is an important reactive oxygen species.Unlike • O − 2, which has reducing properties, HO • 2 can act as an oxidant in a number of biologically important reactions, such as the abstraction of hydrogen atoms from tocopherol and polyunstaturated fatty acids in the lipid bilayer.

  3. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with ...

  4. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    The reaction mechanism involves a two-stage radical process: electrochemical decarboxylation gives a radical intermediate, which combine to form a covalent bond. [2] As an example, electrolysis of acetic acid yields ethane and carbon dioxide: CH 3 COOH → CH 3 COO − → CH 3 COO· → CH 3 · + CO 2 2CH 3 · → CH 3 CH 3

  5. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Industrially, it is prepared by carboalkoxylation, i.e., the reaction of ethylene with carbon monoxide and methanol in the presence of a catalyst: C 2 H 4 + CO + MeOH → MeO 2 CCH 2 CH 3 The reaction is catalyzed by nickel carbonyl and palladium(0) complexes.

  6. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    Important compounds made in this way include tert-butyl hydroperoxide, cumene hydroperoxide and ethylbenzene hydroperoxide: [7] R−H + O 2 → R−OOH. Auto-oxidation reaction is also observed with common ethers, such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane. An illustrative product is diethyl ether peroxide.

  7. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The first reaction with many volatile organic compounds (VOCs) is the removal of a hydrogen atom, forming water and an alkyl radical (R •): • HO + RH → H 2 O + R • The alkyl radical will typically react rapidly with oxygen forming a peroxy radical: R • + O 2 → RO 2

  8. Metal acetylacetonates - Wikipedia

    en.wikipedia.org/wiki/Metal_acetylacetonates

    This reaction requires no base. Under atmospheric conditions the dibromo complex is easily hydrolyzed (1 hr), whereas the dichloro and difluoro complexes are not easily hydrolyzed (1-3 days). The complex TiCl 2 (acac) 2 is fluxional in solution, the NMR spectrum exhibiting a single methyl resonance at room temperature.

  9. Ketene - Wikipedia

    en.wikipedia.org/wiki/Ketene

    In organic chemistry, a ketene is an organic compound of the form RR'C=C=O, where R and R' are two arbitrary monovalent chemical groups (or two separate substitution sites in the same molecule). [1] The name may also refer to the specific compound ethenone H 2 C=C=O, the simplest ketene. [2] Although they are highly useful, most ketenes are ...