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  2. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cistrans_isomerism

    The cis isomer in this case has a boiling point of 60.3 °C, while the trans isomer has a boiling point of 47.5 °C. [6] In the cis isomer the two polar C–Cl bond dipole moments combine to give an overall molecular dipole, so that there are intermolecular dipole–dipole forces (or Keesom forces), which add to the London dispersion forces and ...

  3. 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]

  4. Carbohydrate conformation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_conformation

    The chair conformation of six-membered rings have a dihedral angle of 60° between adjacent substituents thus usually making it the most stable conformer. Since there are two possible chair conformation steric and stereoelectronic effects such as the anomeric effect, 1,3-diaxial interactions, dipoles and intramolecular hydrogen bonding must be taken into consideration when looking at relative ...

  5. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    A: antiperiplanar, anti or trans. B: synclinal or gauche. C: anticlinal or eclipsed. D: synperiplanar or cis. [2] Rotating their carbon–carbon bonds, the molecules ethane and propane have three local energy minima. They are structurally and energetically equivalent, and are called the staggered conformers.

  6. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    Double bond isomers are always considered diastereomers, not enantiomers. Diastereomerism can also occur at a double bond, where the cis vs trans relative positions of substituents give two non-superposable isomers. Many conformational isomers are diastereomers as well.

  7. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    Trans-alkenes are about 1 kcal/mol more stable than cis-alkenes. An example of this effect is cis- vs trans-2-butene. The difference is attributed to unfavorable non-bonded interactions in the cis isomer. Terminal alkenes isomerize to internal alkenes in the presence of metal catalysts.

  8. Isomerase - Wikipedia

    en.wikipedia.org/wiki/Isomerase

    This category (EC 5.2) includes enzymes that catalyze the isomerization of cis-trans isomers. Alkenes and cycloalkanes may have cis-trans stereoisomers. These isomers are not distinguished by absolute configuration but rather by the position of substituent groups relative to a plane of reference, as across a double bond or relative to a ring ...

  9. 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