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  2. Transalkylation - Wikipedia

    en.wikipedia.org/wiki/Transalkylation

    The reaction is used for the transfer of methyl and ethyl groups between benzene rings. This is of particular value in the petrochemical industry [1] to manufacture p-xylene, styrene, [2] and other aromatic compounds. Motivation for using transalkylation reactions is based on a difference in production and demand for benzene, toluene, and xylenes.

  3. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene is also found in cigarette smoke and car exhaust. If not in contact with air, toluene can remain unchanged in soil or water for a long time. [39] Toluene is a common solvent, e.g. for paints, paint thinners, silicone sealants, [40] many chemical reactants, rubber, printing ink, adhesives (glues), lacquers, leather tanners, and ...

  4. Dean–Stark apparatus - Wikipedia

    en.wikipedia.org/wiki/Dean–Stark_apparatus

    This piece of equipment is usually used in azeotropic distillations. A common example is the removal of water generated during a reaction in boiling toluene . An azeotropic mixture of toluene and water distills out of the reaction, but only the toluene (density 0.865 g/ml) returns, since it floats on top of the water (density 0.998 g/ml), which ...

  5. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid. [5] Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring. [4]

  6. Hydrodealkylation - Wikipedia

    en.wikipedia.org/wiki/Hydrodealkylation

    Hydrodealkylation is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of hydrogen gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. [1]

  7. Ring-closing metathesis - Wikipedia

    en.wikipedia.org/wiki/Ring-closing_metathesis

    Ring-closing metathesis (RCM) is a widely used variation of olefin metathesis in organic chemistry for the synthesis of various unsaturated rings via the intramolecular metathesis of two terminal alkenes, which forms the cycloalkene as the E-or Z-isomers and volatile ethylene.

  8. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    The methyl group in toluene is small and will lead the ortho product being the major product. On the other hand, the t-butyl group is very bulky (there are 3 methyl groups attached to a single carbon) and will lead the para product as the major one. Even with toluene, the product is not 2:1 but having a slightly less ortho product.

  9. Acyloin condensation - Wikipedia

    en.wikipedia.org/wiki/Acyloin_condensation

    The reaction is performed in aprotic solvents with a high boiling point, such as benzene and toluene, in an oxygen-free atmosphere (as even traces of oxygen interfere with the reaction path and reduce the yield). Protic solvents effect the Bouveault-Blanc ester reduction rather than condensation

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