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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. Cyclohexanedimethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedimethanol

    A copper chromite catalyst is usually used industrially. [1] The cis/trans ratio of the CHDM is affected by the catalyst. [2] Byproduct of this process are 4-methylcyclohexanemethanol (CH 3 C 6 H 10 CH 2 OH) and the monoester methyl 4-methyl-4-cyclohexanecarboxylate (CH 3 C 6 H 10 CO 2 CH 3, CAS registry number 51181-40-9). [3]

  4. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    An example of interactions within a molecule that would lead to steric strain, leading to a shift in equilibrium from boat to chair, is the interaction between the two methyl groups in cis-1,4-dimethylcyclohexane.

  5. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  6. 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.

  7. AOL

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    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  8. 1,2-Diaminocyclohexane - Wikipedia

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

    1,2-Diaminocyclohexane (DACH) is an organic compound with the formula (CH 2) 4 (CHNH 2) 2. It is a mixture of three stereoisomers: cis-1,2-diaminocyclohexane and both enantiomers of trans-1,2-diaminocyclohexane. The mixture is a colorless, corrosive liquid, although older samples can appear yellow. It is often called DCH-99 and also DACH.

  9. Can alcohol cause cancer? Here's what the science says

    www.aol.com/alcohol-cause-cancer-heres-science...

    A Scotch neat has an alcohol by volume (ABV) level upwards of 40%, while a Modelo, America's most popular beer has 4.4% ABV, and a White Claw hard seltzer, 5%.