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  2. 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.

  3. 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 .

  4. 1-Hexene (data page) - Wikipedia

    en.wikipedia.org/wiki/1-Hexene_(data_page)

    2 Structure and properties. 3 Thermodynamic properties. 4 Spectral data. ... This page provides supplementary chemical data on 1-Hexene. Material Safety Data Sheet

  5. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.

  6. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    In 1 H NMR spectroscopy, the hydrogen bonded to the carbon adjacent to double bonds will give a δ H of 4.5–6.5 ppm. The double bond will also deshield the hydrogen attached to the carbons adjacent to sp 2 carbons, and this generates δ H =1.6–2. ppm peaks. [14] Cis/trans isomers are distinguishable due to different J-coupling effect.

  7. 1-Hexyne - Wikipedia

    en.wikipedia.org/wiki/1-Hexyne

    1-Hexyne can be prepared by the reaction of monosodium acetylide with butyl bromide: [1] NaC 2 H + BrC 4 H 9 → HC 2 C 4 H 9 + NaBr. Its reactivity illustrates the behavior of terminal alkylacetylenes. The hexyl derivative is common test substrate because it is conveniently volatile. It undergoes deprotonation at C-3 and C-1 with butyl lithium:

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    www.aol.com/costco-just-issued-recall-popular...

    You can also reach out to LNK International, the manufacturers of the over-the-counter medicine, at 1-800-426-9391 or email complaints-inquiries@lnkintl.com if you have any questions or concerns.

  9. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    3,3-dimethylbut-1-yne This page was last edited on 22 May 2021, at 18:45 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...