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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. 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.

  4. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Critical point. 554 K (281 °C), 4070 kPa. Std enthalpy change of fusion, Δ fusH o. 2.68 kJ/mol crystal I → liquid. Std entropy change of fusion, Δ fusS o. 9.57 J/ (mol·K) crystal I → liquid. Std enthalpy change of vaporization, Δ vapH o. 32 kJ/mol. Std entropy change of vaporization, Δ vapS o.

  5. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Structural isomer. In chemistry, a structural isomer (or constitutional isomer in the IUPAC nomenclature [ 1 ]) of a compound is another compound whose molecule has the same number of atoms of each element, but with logically distinct bonds between them. [ 2 ][ 3 ] The term metamer was formerly used for the same concept. [ 4 ]

  6. 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 ...

  7. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    trans -but-2-ene. Cis–trans isomerism, also known as geometric isomerism, describes certain arrangements of atoms within molecules. The prefixes " cis " and " trans " are from Latin: "this side of" and "the other side of", respectively. [ 1 ] In the context of chemistry, cis indicates that the functional groups (substituents) are on the same ...

  8. 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]

  9. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [1] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes. A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom ...