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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    For 1,2- and 1,4-disubstituted cyclohexane, a trans configuration, the diaxial conformation is effectively prevented by its high steric strain. For 1,3-disubstituted cyclohexanes, the cis form is diequatorial and the flipped conformation suffers additional steric interaction between the two axial groups.

  3. 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.

  4. 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.

  5. File:Trans-1,2-Diaminocyclohexane Structural Formulae V.1.svg

    en.wikipedia.org/wiki/File:Trans-1,2-Diaminocyc...

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  6. Trost ligand - Wikipedia

    en.wikipedia.org/wiki/Trost_ligand

    The Trost ligand is a diphosphine used in the palladium-catalyzed Trost asymmetric allylic alkylation.Other C 2-symmetric ligands derived from trans-1,2-diaminocyclohexane (DACH) have been developed, such as the (R,R)-DACH-naphthyl ligand derived from 2-diphenylphosphino-1-naphthalenecarboxylic acid.

  7. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes . Cycloalkanes

  8. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  9. 1,2-Dibromoethylene - Wikipedia

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

    1,2-Dibromoethylene, also known as 1,2-dibromoethene and acetylene dibromide, is a dihalogenated unsaturated compound with one bromine on each of the two carbon atoms. There are two isomers of this compound, cis and trans. Both isomers are colorless liquids.