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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    A cyclohexane molecule in chair conformation. Hydrogen atoms in axial positions are shown in red, while those in equatorial positions are in blue. Cyclohexane conformations are any of several three-dimensional shapes adopted by molecules of cyclohexane. Because many compounds feature structurally similar six-membered rings, the structure and ...

  3. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    Alkyl cycloalkanes are chemical compounds with an alkyl group with a single ring of carbons to which hydrogens are attached according to the formula. C n H 2n. They are named analogously to their normal alkane counterpart of the same carbon count: methylcyclopropane, methylcyclobutane, methylcyclopentane, methylcyclohexane, etc. [1 ...

  4. 1,2-Dimethylcyclopropane - Wikipedia

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

    1,2-Dimethylcyclopropane is a cycloalkane consisting of a cyclopropane ring substituted with two methyl groups attached to adjacent carbon atoms. [1] It has three stereoisomers, one cis -isomer and a pair of trans - enantiomers, which differ depending on the orientation of the two methyl groups. As with other cyclopropanes, ring tension results ...

  5. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Methylcyclohexane(cyclohexylmethane) is an organic compoundwith the molecular formula is CH3C6H11. Classified as saturated hydrocarbon, it is a colourless liquidwith a faint odor. Methylcyclohexane is used as a solvent. It is mainly converted in naphtha reformersto toluene.[4]

  6. Conformational isomerism - Wikipedia

    en.wikipedia.org/wiki/Conformational_isomerism

    Conformational isomerism. Rotation about single bond of butane to interconvert one conformation to another. The gauche conformation on the right is a conformer, while the eclipsed conformation on the left is a transition state between conformers. Above: Newman projection; below: depiction of spatial orientation.

  7. trans-1,2-Diaminocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Trans-1,2-Diaminocyclohexane

    trans-1,2-Diaminocyclohexane is an organic compound with the formula C 6 H 10 (NH 2) 2. This diamine is a building block for C 2-symmetric ligands that are useful in asymmetric catalysis. [1] A mixture of all three stereoisomers of 1,2-diaminocyclohexane is produced by the hydrogenation of o-phenylenediamine.

  8. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    List of straight-chain alkanes. The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ][ 2 ] Number of C atoms. Number of isomers [ 3 ][ 4 ]

  9. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.