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  2. Raschig–Hooker process - Wikipedia

    en.wikipedia.org/wiki/Raschig–Hooker_process

    The Raschig–Hooker process is a chemical process for the production of chlorobenzene and phenol. [1][2] The Raschig–Hooker process was patented by Friedrich Raschig, a German chemist and politician also known for the Raschig process, the Olin Raschig process and the Raschig ring. [3] He first begun to use this reaction in 1891 in order to ...

  3. Rust converter - Wikipedia

    en.wikipedia.org/wiki/Rust_converter

    Rust converter. Rust converters are chemical solutions or primers that can be applied directly to an iron or iron alloy surface to convert iron oxides (rust) into a protective chemical barrier. These compounds interact with iron oxides, especially iron (III) oxide, converting them into an adherent black layer (black oxide) that is more ...

  4. Dow process (phenol) - Wikipedia

    en.wikipedia.org/wiki/Dow_process_(phenol)

    Details. Benzene can be easily converted to chlorobenzene by nucleophilic aromatic substitution via a benzyne intermediate. [1] It is treated with aqueous sodium hydroxide at 350 °C and 300 bar or molten sodium hydroxide at 350 °C to convert it to sodium phenoxide, which yields phenol upon acidification. [2] When 1- [14 C]-1-chlorobenzene was ...

  5. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline solid that is volatile . The molecule consists of a phenyl group ( −C 6 H 5 ) bonded to a hydroxy group ( −OH ).

  6. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

  7. Benzoin condensation - Wikipedia

    en.wikipedia.org/wiki/Benzoin_condensation

    Benzoin condensation. The benzoin addition is an addition reaction involving two aldehydes. The reaction generally occurs between aromatic aldehydes or glyoxals, [1][2] and results in formation of an acyloin. In the classic example, benzaldehyde is converted to benzoin. [3]

  8. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    RXNO:0000021. The Sandmeyer reaction is a chemical reaction used to synthesize aryl halides from aryl diazonium salts using copper salts as reagents or catalysts. [1][2][3][4] It is an example of a radical-nucleophilic aromatic substitution. The Sandmeyer reaction provides a method through which one can perform unique transformations on benzene ...

  9. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    Gattermann reaction. The Gattermann reaction (also known as the Gattermann formylation and the Gattermann salicylaldehyde synthesis) is a chemical reaction in which aromatic compounds are formylated by a mixture of hydrogen cyanide (HCN) and hydrogen chloride (HCl) in the presence of a Lewis acid catalyst such as aluminium chloride (AlCl 3). [1 ...