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  2. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Although not practiced under the name, aromatization is a cornerstone of oil refining. One of the major reforming reactions is the dehydrogenation of paraffins and naphthenes into aromatics. The process, which is catalyzed by platinum supported by aluminium oxide, is exemplified in the conversion methylcyclohexane (a naphthene) into toluene (an ...

  3. Demulsifier - Wikipedia

    en.wikipedia.org/wiki/Demulsifier

    Commercially available demulsifier formulations are typically a mixture of two to four different chemistries, in carrier solvent(s) such as xylene, heavy aromatic naphtha (HAN), Isopropanol, methanol, 2-Ethylhexanol or diesel. Demulsifiers are manufactured by chemical manufacturers including: Arkema; Baker Hughes; BASF; ChampionX; Clariant; Dow ...

  4. 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 ...

  5. Oxygenate - Wikipedia

    en.wikipedia.org/wiki/Oxygenate

    In the liquid fuel industry, oxygenates are hydrocarbon-derived fuel additives containing at least one oxygen atom [1] to promote complete combustion. [2] Absent oxygenates, fuel combustion is usually incomplete, and the exhaust stream pollutes the air with carbon monoxide, soot particles, aromatic and polyaromatic hydrocarbons, and nitrated polyaromatic hydrocarbons.

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, (CH 3) 2 CHCH 2 CH 3 (isopentane) is named 2-methylbutane, not 3-methylbutane. If there are multiple side-branches of the same size alkyl group, their positions are separated by commas and the group prefixed with multiplier prefixes depending on the number of branches. For example, C(CH 3) 4 (neopentane) is named 2,2 ...

  7. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    Alkenes are precursors to aldehydes (R−CH=O), alcohols (R−OH), polymers, and aromatics. [1] As a problematic reaction, the fouling and inactivation of many catalysts arises via coking, which is the dehydrogenative polymerization of organic substrates. [2] Enzymes that catalyze dehydrogenation are called dehydrogenases.

  8. Aromatic alcohol - Wikipedia

    en.wikipedia.org/wiki/Aromatic_alcohol

    In organic chemistry, the aromatic alcohols or aryl-alcohols are a class of chemical compounds containing a hydroxyl group (−O H) bonded indirectly to an aromatic hydrocarbon group, [1] in contrast to the phenols, where the hydroxyl group is bonded directly to an aromatic carbon atom. [2] Aromatic alcohols are produced by the yeast Candida ...

  9. Petrochemical - Wikipedia

    en.wikipedia.org/wiki/Petrochemical

    Petrochemical plant in Saudi Arabia. Petrochemicals (sometimes abbreviated as petchems [1]) are the chemical products obtained from petroleum by refining. Some chemical compounds made from petroleum are also obtained from other fossil fuels, such as coal or natural gas, or renewable sources such as maize, palm fruit or sugar cane.