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  2. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Most aliphatic compounds are flammable, allowing the use of hydrocarbons as fuel, such as methane in natural gas for stoves or heating; butane in torches and lighters; various aliphatic (as well as aromatic) hydrocarbons in liquid transportation fuels like petrol/gasoline, diesel, and jet fuel; and other uses such as ethyne (acetylene) in welding.

  3. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    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 nitrogen atom. Hydrocarbons without an aromatic ring are called aliphatic. Approximately half of compounds known ...

  4. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Aromatic hydrocarbons, also known as arenes, which are hydrocarbons that have at least one aromatic ring. 10% of total nonmethane organic carbon emission are aromatic hydrocarbons from the exhaust of gasoline-powered vehicles. [4] The term 'aliphatic' refers to non-aromatic hydrocarbons.

  5. Naphthenic oil - Wikipedia

    en.wikipedia.org/wiki/Naphthenic_oil

    These include, for example, plasticizers in polymer-based formulations, rheology modifier in printing inks and carrier oil in anti-foaming agents. Naphthenic oils have been proven to be suitable in the tyre oils segment because of their low content of polycyclic aromatic hydrocarbons (PAHs), which are hazardous to health and the environment. 3.

  6. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    As of alkanes, they first dehydrogenate to olefins, then form rings at the place of the double bond, becoming cycloalkanes, and finally gradually lose hydrogen to become aromatic hydrocarbons. [ 4 ] For cyclohexane, cyclohexene, and cyclohexadiene, dehydrogenation is the conceptually simplest pathway for aromatization.

  7. Petroleum ether - Wikipedia

    en.wikipedia.org/wiki/Petroleum_ether

    Petroleum ether consists mainly of aliphatic hydrocarbons and is usually low in aromatics. It is commonly hydrodesulfurized and may be hydrogenated to reduce the amount of aromatic and other unsaturated hydrocarbons. Petroleum ether bears normally a descriptive suffix giving the boiling range.

  8. Hydrocarbon mixtures - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon_mixtures

    A hydrocarbon is any chemical compound that consists only of the elements carbon (C) and hydrogen (H). They all contain a carbon frame, and have hydrogen atoms attached to the frame. Often the term is used as a shortened form of the term aliphatic hydrocarbon. Most hydrocarbons are combustible. [2]

  9. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...