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  2. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    Aromatic alcohols (example: tyrosol) are produced by the yeast Candida albicans. [47] They are also found in beer. [48] These molecules are quorum sensing compounds for Saccharomyces cerevisiae. [49] Metabolism. Aryl-alcohol dehydrogenase uses an aromatic alcohol and NAD + to produce an aromatic aldehyde, NADH and H +.

  3. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    The aromatic products of the reaction are then separated from the reaction mixture (or reformate) by extraction with any one of a number of solvents, including diethylene glycol or sulfolane, and benzene is then separated from the other aromatics by distillation. The extraction step of aromatics from the reformate is designed to produce ...

  4. BTX (chemistry) - Wikipedia

    en.wikipedia.org/wiki/BTX_(chemistry)

    In the petroleum refining and petrochemical industries, the initialism BTX refers to mixtures of benzene, toluene, and the three xylene isomers, all of which are aromatic hydrocarbons. The xylene isomers are distinguished by the designations ortho – (or o –), meta – (or m –), and para – (or p –) as indicated in the adjacent diagram.

  5. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...

  6. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene. Aromatization includes the formation of heterocyclic systems. [1]

  7. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    Xylenes are produced mainly as part of the BTX aromatics (benzene, toluene, and xylenes) extracted from the product of catalytic reforming known as reformate. Several million tons are produced annually. [3] In 2011, a global consortium began construction of one of the world's largest xylene plants in Singapore. [5]

  8. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    The production of p-xylene is industrially significant, with annual demand estimated at 37 million tons in 2014, and still on the increase. [12] [13] p-Xylene is produced by catalytic reforming of petroleum naphtha as part of the BTX aromatics (benzene, toluene and the xylene isomers) extracted from the catalytic reformate.

  9. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    In chemistry, a phenol ether (or aromatic ether) is an organic compound derived from phenol (C 6 H 5 OH), where the hydroxyl (-OH) group is substituted with an alkoxy (-OR) group. Usually phenol ethers are synthesized through the condensation of phenol and an organic alcohol ; however, other known reactions regarding the synthesis of ethers can ...