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  2. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cistrans_isomerism

    For example, there are two isomers of square planar Pt(NH 3) 2 Cl 2, as explained by Alfred Werner in 1893. The cis isomer, whose full name is cis -diamminedichloroplatinum(II), was shown in 1969 by Barnett Rosenberg to have antitumor activity, and is now a chemotherapy drug known by the short name cisplatin .

  3. 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 ...

  4. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    The branched isomers are 2-methylbut-1-ene, 3-methylbut-1-ene (isopentene), and 2-methylbut-2-ene (isoamylene). Isoamylene is one of the three main byproducts of deep catalytic cracking (DCC), which is very similar to the operation of fluid catalytic cracking (FCC).

  5. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Traditionally, double bond stereochemistry was described as either cis (Latin, on this side) or trans (Latin, across), in reference to the relative position of substituents on either side of a double bond. A simple example of cistrans isomerism is the 1,2-disubstituted ethenes, like the dichloroethene (C 2 H 2 Cl 2) isomers shown below. [7]

  6. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

    The molecular formula C 6 H 12 may refer to following structural isomers ... 4-Methyl-2-pentene; Dimethylbutenes. 2,3-Dimethyl-1-butene ... cis-trans isomers and ...

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For example, of the isomers of butene, the two methyl groups of (Z)-but-2-ene (a.k.a. cis-2-butene) appear on the same side of the double bond, and in (E)-but-2-ene (a.k.a. trans-2-butene) the methyl groups appear on opposite sides. These two isomers of butene have distinct properties.

  8. 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 ...

  9. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    The reaction is highly stereospecific in the sense that the double bond stereochemistry is generally transferred to the relative configuration of the epoxide with essentially perfect fidelity, so that a trans-olefin leads to the stereoselective formation of the trans-2,3-substituted epoxide only, as illustrated by the example above, while a cis ...