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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene is widely used in the chemical industry, and its worldwide production (over 150 million tonnes in 2016 [8]) exceeds that of any other organic compound. [9] [10] Much of this production goes toward creating polythene, which is a widely used plastic containing polymer chains of ethylene units in various chain lengths.

  3. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide is an organic compound with the formula C 2 H 4 O.It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms.

  4. Ethylene (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethylene_(data_page)

    Phase behavior Triple point: 104 K (−169 °C), 120 Pa Critical point: 282.5 K (9.4 °C), 50.6 bar Std enthalpy change of fusion, Δ fus H o +3.35 kJ/mol Std entropy change

  5. Ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Ethylenediamine

    Ethylenediamine (abbreviated as en when a ligand) is the organic compound with the formula C 2 H 4 (NH 2) 2.This colorless liquid with an ammonia-like odor is a basic amine.It is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998. [6]

  6. Polyethylene - Wikipedia

    en.wikipedia.org/wiki/Polyethylene

    Polyethylene was first synthesized by the German chemist Hans von Pechmann, who prepared it by accident in 1898 while investigating diazomethane. [12] [a] [13] [b] When his colleagues Eugen Bamberger and Friedrich Tschirner characterized the white, waxy substance that he had created, they recognized that it contained long −CH 2 − chains and termed it polymethylene.

  7. Zeise's salt - Wikipedia

    en.wikipedia.org/wiki/Zeise's_salt

    [4] [5] In Zeise's salt and related compounds, the alkene rotates about the metal-alkene bond with a modest activation energy. Analysis of the barrier heights indicates that the π-bonding between most metals and the alkene is weaker than the σ-bonding. In Zeise's anion, this rotational barrier has not been assessed.

  8. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    Numerous organic compounds have other common names, often originating in historical source material thereof. The systematic IUPAC name is not always the preferred IUPAC name , for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid.

  9. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms. An industrially important example is vinyl chloride, precursor to PVC, [3] a plastic commonly known as vinyl. Chessboard made from polyvinyl chloride. Vinyl is one of the alkenyl functional groups.