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  2. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol is reduced to benzene when it is distilled with zinc dust or when its vapour is passed over granules of zinc at 400 °C: [22] C 6 H 5 OH + Zn → C 6 H 6 + ZnO. When phenol is treated with diazomethane in the presence of boron trifluoride (BF 3), anisole is obtained as the main product and nitrogen gas as a byproduct. C 6 H 5 OH + CH 2 N ...

  3. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    The term stems from cumene (isopropyl benzene), the intermediate material during the process. It was invented by R. Ūdris and P. Sergeyev in 1942 (USSR), [1] and independently by Heinrich Hock in 1944. [2] [3] This process converts two relatively cheap starting materials, benzene and propylene, into two more valuable ones, phenol and acetone.

  4. Birch reduction - Wikipedia

    en.wikipedia.org/wiki/Birch_reduction

    Birch reduction of benzene, also available in animated form. The reaction is known to be third order – first order in the aromatic, first order in the alkali metal, and first order in the alcohol. [4] This requires that the rate-limiting step be the conversion of radical anion B to the cyclohexadienyl radical C. Birch reduction of anisole.

  5. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    reduction of quinones; replacement of an aromatic amine by an hydroxyl group with water and sodium bisulfide in the Bucherer reaction [11] thermal decomposition of aryl diazonium salts, the salts are converted to phenol [12] by the oxidation of aryl silanes—an aromatic variation of the Fleming-Tamao oxidation [13]

  6. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process:

  7. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is an organic chemical compound with the molecular formula C 6 H 6. ... Birch reduction, ... converting benzene to oxepin (benzene oxide), phenol to ...

  8. Raschig–Hooker process - Wikipedia

    en.wikipedia.org/wiki/Raschig–Hooker_process

    [6] [7] Due to the two step nature, the Raschig–Hooker process can be used to produce either chlorobenzene or phenol. Reaction scheme of the Raschig-Hooker process. The Raschig–Hooker process's ability to make phenol makes it comparable to other methods, such as the Dow and Bayer process, which also converts benzene into phenol. In fact ...

  9. Blanc chloromethylation - Wikipedia

    en.wikipedia.org/wiki/Blanc_chloromethylation

    The Blanc chloromethylation (also called the Blanc reaction) is the chemical reaction of aromatic rings with formaldehyde and hydrogen chloride to form chloromethyl arenes. . The reaction is catalyzed by Lewis acids such as zinc chlorid