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  2. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12.The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond.

  3. File: (E)-hex-2-ene 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:(E)-hex-2-ene_200.svg

    This structural formula was created with Name2Struct - CS ChemDraw Ultra. The chemistry symbols of this structural formula are drawn using the path text method. The accuracy of this version of the structural formula has been verified as part of the Chemical Structure Validation project .

  4. File:(Z)-hex-3-ene 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:(Z)-hex-3-ene_200.svg

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  5. 1-Hexene - Wikipedia

    en.wikipedia.org/wiki/1-Hexene

    1-Hexene (hex-1-ene) is an organic compound with the formula C 6 H 12.It is an alkene that is classified in industry as higher olefin and an alpha-olefin, the latter term meaning that the double bond is located at the alpha (primary) position, endowing the compound with higher reactivity and thus useful chemical properties. 1-Hexene is an industrially significant linear alpha olefin.

  6. Help:Displaying a formula - Wikipedia

    en.wikipedia.org/wiki/Help:Displaying_a_formula

    This screenshot shows the formula E = mc 2 being edited using VisualEditor.The window is opened by typing "<math>" in VisualEditor. The visual editor shows a button that allows to choose one of three offered modes to display a formula.

  7. 5-oxopent-3-ene-1,2,5-tricarboxylate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/5-oxopent-3-ene-1,2,5-tri...

    Other names in common use include 5-carboxymethyl-2-oxo-hex-3-ene-1,6-dioate decarboxylase, and 5-oxopent-3-ene-1,2,5-tricarboxylate carboxy-lyase. This enzyme participates in tyrosine metabolism . Structural studies

  8. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]

  9. 2-Hexyne - Wikipedia

    en.wikipedia.org/wiki/2-Hexyne

    2-Hexyne can be semihydrogenated to yield 2-hexene or fully hydrogenated to hexane. [3] With appropriate noble metal catalysts it can selectively form cis-2-hexene. [4] 2-Hexyne can act as a ligand on gold atoms. [5] With strong sulfuric acid, the ketone 2-hexanone is produced. However this reaction also causes polymerization and charring. [6]