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  2. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cistrans_isomerism

    Cistrans isomers are stereoisomers, that is, pairs of molecules which have the same formula but whose functional groups are in different orientations in three-dimensional space. Cis and trans isomers occur both in organic molecules and in inorganic coordination complexes.

  3. 1,3-Dichloropropene - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropene

    1,3-Dichloropropene, sold under diverse trade names, is an organochlorine compound with the formula C 3 H 4 Cl 2.It is a colorless liquid with a sweet smell. It is feebly soluble in water and evaporates easily.

  4. 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]

  5. 1,2-Dibromoethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethylene

    Chemical formula. C 2 H 2 Br 2: Molar mass: 185.846 g·mol −1 ... There are two isomers of this compound, cis and trans. Both isomers are colorless liquids. Synthesis

  6. Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctene

    Possible isomers of cyclooctene. Cyclooctene is the cycloalkene with a formula C 8 H 14. Its molecule has a ring of 8 carbon atoms, connected by seven single bonds and one double bond. Cyclooctene is notable because it is the smallest cycloalkene that can exist stably as either the cis or trans stereoisomer, with cis-cyclooctene being the

  7. Cyclodecapentaene - Wikipedia

    en.wikipedia.org/wiki/Cyclodecapentaene

    The nonplanar transciscisciscis isomer is the most stable of all possible isomers, [citation needed] although it is unclear whether it too has a boat-like configuration as in conformer , or the "heart" configuration produced if one internal hydrogen in conformer were flipped inside-out. [2]

  8. (1R,3R)-1,2,3-Trimethylcyclopentane - Wikipedia

    en.wikipedia.org/wiki/(1R,3R)-1,2,3-trimethylcyc...

    The methyl groups off carbons 1 and 3 are trans with respect to each other, while the methyl group off carbon 2 has undefined stereochemistry, allowing it to be either cis or trans with respect to methyl 1 or 3. [2] Each carbon atom within the cyclopentane ring is sp 3 hybridized with the theoretical C-C-C bond angles near 108 degrees.

  9. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    And each of these cis-trans isomers can possibly have stable "chair" or "boat" conformations (although the barriers between these are significantly lower than those between different cis-trans isomers). The two isomeric complexes, cisplatin and transplatin, are examples of square planar MX 2 Y 2 molecules with M = Pt.