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  2. Alkylation - Wikipedia

    en.wikipedia.org/wiki/Alkylation

    Typical route for alkylation of benzene with ethylene and ZSM-5 as a heterogeneous catalyst. Alkylation is a chemical reaction that entails transfer of an alkyl group. The alkyl group may be transferred as an alkyl carbocation, a free radical, a carbanion, or a carbene (or their equivalents).

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  4. BTX (chemistry) - Wikipedia

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

    The BTX aromatics can be extracted from catalytic reformate or from pyrolysis gasoline by many different methods. Most of those methods, but not all, involve the use of a solvent either for liquid-liquid extraction or extractive distillation.

  5. Alkylated naphthalene - Wikipedia

    en.wikipedia.org/wiki/Alkylated_naphthalene

    Alkylated naphthalenes are chemical compounds made by the alkylation of naphthalene or its derivatives with an olefin. These compounds are used as synthetic base oils, and are claimed to have improved oxidative stability over some conventional base oils.

  6. 1,4-Naphthoquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-Naphthoquinone

    1,4-Naphthoquinone or para-naphthoquinone is a quinone derived from naphthalene. It forms volatile yellow triclinic crystals and has a sharp odor similar to benzoquinone. It is almost insoluble in cold water, slightly soluble in petroleum ether, and more soluble in polar organic solvents. In alkaline solutions it produces a reddish-brown color ...

  7. Sodium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Sodium_naphthalene

    Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]

  8. Phthalic anhydride - Wikipedia

    en.wikipedia.org/wiki/Phthalic_anhydride

    The naphthalene route (the Gibbs phthalic anhydride process or the Gibbs–Wohl naphthalene oxidation reaction) has declined relative to the o-xylene route. Proposed early steps in vanadium -catalyzed oxidation of naphthalene to phthalic anhydride, with V 2 O 5 represented as a molecule versus its true extended structure.

  9. Naphthalene 1,2-dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Naphthalene_1,2-dioxygenase

    The systematic name of this enzyme class is naphthalene,NADH:oxygen oxidoreductase (1,2-hydroxylating). Other names in common use include naphthalene dioxygenase , and naphthalene oxygenase . This enzyme participates in 4 metabolic pathways : 1- and 2-methylnaphthalene degradation , naphthalene and anthracene degradation , fluorene degradation ...