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  2. 2,4-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,4-Dimethylpentane

    2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.

  3. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.

  4. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Because the cis–trans and E–Z systems compare different groups on the alkene, it is not strictly true that Z corresponds to cis and E corresponds to trans. For example, trans-2-chlorobut-2-ene (the two methyl groups, C1 and C4, on the but-2-ene backbone are trans to each other) is (Z)-2-chlorobut-2-ene (the chlorine and C4 are together ...

  5. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... cis-2-Pentene (CAS 627-20-3) trans-2-pentene (CAS 646-04-8 ...

  6. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    The cis isomer exclusively yields cis,trans-hexa-2,4-diene whereas the trans isomer gives the trans,trans diene: [2] This reaction course can be explained in a simple analysis through the frontier-orbital method: the sigma bond in the reactant will open in such a way that the resulting p-orbitals will have the same symmetry as the HOMO of the ...

  7. Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/Dimethylpentane

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  8. Hydroboration - Wikipedia

    en.wikipedia.org/wiki/Hydroboration

    Hydroboration of 1,2-disubstituted alkenes, such as a cis or trans olefin, produces generally a mixture of the two organoboranes of comparable amounts, even if the steric properties of the substituents are very different. For such 1,2-disubstituted olefins, regioselectivity can be observed only when one of the two substituents is a phenyl ring.

  9. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    9 – MgBr with acetone to form 2,3-dimethyl-2-pentanol, then dehydrating this alcohol to form 2,3-dimethyl-2-pentene, and hydrogenating this product. [ 4 ] The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture ...