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  2. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    In the Tishchenko reaction, the base used is an alkoxide rather than hydroxide, and the product is an ester rather than the separate alcohol and carboxylate groups. After the nucleophilic base attacks an aldehyde, the resulting new oxygen anion attacks another aldehyde to give a hemiacetal linkage between two of the formerly aldehyde-containing ...

  3. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    An alcohol solution of potassium hydroxide decomposes it to potassium chloride and potassium carbonate in water: [11] CCl 4 + 6 KOH → 4 KCl + K 2 CO 3 + 3 H 2 O. Carbon is sufficiently oxophilic that many compounds react to give phosgene:

  4. Potassium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Potassium_hydroxide

    Preshave products and some shave creams contain potassium hydroxide to force open the hair cuticle and to act as a hygroscopic agent to attract and force water into the hair shaft, causing further damage to the hair. In this weakened state, the hair is more easily cut by a razor blade. Potassium hydroxide is used to identify some species of ...

  5. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Some metal-organic coordination compounds can eliminate hydrogen halides, [6] either spontaneously, [7] thermally, or by mechanochemical reaction with a solid base such as potassium hydroxide. [8] For example, salts that contain acidic cations hydrogen bonded to halometallate anions will often undergo dehydrohalogenation reactions reversibly: [6]

  6. Carbylamine reaction - Wikipedia

    en.wikipedia.org/wiki/Carbylamine_reaction

    In this reaction, the analyte is heated with alcoholic potassium hydroxide and chloroform. If a primary amine is present, the isocyanide (carbylamine) is formed, as indicated by a foul odour. The carbylamine test does not give a positive reaction with secondary and tertiary amines.

  7. Dichlorocarbene - Wikipedia

    en.wikipedia.org/wiki/Dichlorocarbene

    Dichlorocarbene is an intermediate in the carbylamine reaction. In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase-transfer catalyst. Illustrative is the synthesis of tert-butyl isocyanide: [7]

  8. Methane - Wikipedia

    en.wikipedia.org/wiki/Methane

    Methane (US: / ˈ m ɛ θ eɪ n / METH-ayn, UK: / ˈ m iː θ eɪ n / MEE-thayn) is a chemical compound with the chemical formula CH 4 (one carbon atom bonded to four hydrogen atoms). It is a group-14 hydride, the simplest alkane, and the main constituent of natural gas.

  9. Methane functionalization - Wikipedia

    en.wikipedia.org/wiki/Methane_functionalization

    Shilov et al. then was able to catalytically convert methane into methanol or methyl chloride when a Pt(IV) salt was used as a stoichiometric oxidant. The process is simplified down into three main steps: (1) C-H activation, (2) a redox reaction to form an octahedral intermediate, followed by (3) the formation of the carbon-oxygen bond to form ...