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  2. 1,4-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedione

    1,4-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. This white solid is one of the three isomeric cyclohexanediones . This particular diketone is used as a building block in the synthesis of more complex molecules.

  3. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Molecular geometry influences several properties of a substance including its reactivity, polarity, phase of matter, color, magnetism and biological activity. [ 1 ] [ 2 ] [ 3 ] The angles between bonds that an atom forms depend only weakly on the rest of molecule, i.e. they can be understood as approximately local and hence transferable ...

  4. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    trans-1,3-Disubstituted cyclohexanes are like cis-1,2- and cis-1,4- and can flip between the two equivalent axial/equatorial forms. [ 2 ] Cis -1,4-Di- tert -butylcyclohexane has an axial tert -butyl group in the chair conformation and conversion to the twist-boat conformation places both groups in more favorable equatorial positions.

  5. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  6. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    It was first prepared by the free-radical reaction of cyclohexane using carbon disulfide as a sulfur source. [1]It is produced industrially by the hydrogenation of cyclohexanone in the presence of hydrogen sulfide over a metal sulfide catalyst:

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  8. Cyclohexane (data page) - Wikipedia

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

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions.

  9. Umpolung - Wikipedia

    en.wikipedia.org/wiki/Umpolung

    In organic chemistry, umpolung (German: [ˈʔʊmˌpoːlʊŋ]) or polarity inversion is the chemical modification of a functional group with the aim of the reversal of polarity of that group. [ 1 ] [ 2 ] This modification allows secondary reactions of this functional group that would otherwise not be possible. [ 3 ]