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  2. Cyclobutene - Wikipedia

    en.wikipedia.org/wiki/Cyclobutene

    Cyclobutene is an organic compound with the chemical formula C 4 H 6. It is a cycloalkene. It is a colorless gas that easily condenses. It is of interest in research but currently has no practical applications. A modern synthesis involves the 2-step dehydration of cyclobutanol. [1]

  3. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    Some cycloalkenes, such as cyclobutene and cyclopentene, can be used as monomers to produce polymer chains. [1] Due to geometrical considerations, smaller cycloalkenes are almost always the cis isomers , and the term cis tends to be omitted from the names.

  4. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    Cyclobutane is a cycloalkane and organic compound with the formula (CH 2) 4.Cyclobutane is a colourless gas and is commercially available as a liquefied gas.Derivatives of cyclobutane are called cyclobutanes.

  5. 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.

  6. Cyclobutadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclobutadiene

    The compound is the prototypical antiaromatic hydrocarbon with 4 pi electrons (or π electrons). It is the smallest [n]-annulene ([4]-annulene).Its rectangular structure is the result of a pseudo [3] - (or second order) Jahn–Teller effect, which distorts the molecule and lowers its symmetry, converting the triplet to a singlet ground state. [4]

  7. C4H6 - Wikipedia

    en.wikipedia.org/wiki/C4H6

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  8. Möbius–Hückel concept - Wikipedia

    en.wikipedia.org/wiki/Möbius–Hückel_concept

    Möbius–Hückel correlation diagram; two modes of butadiene to cyclobutene conversion. It has been noted that for every degeneracy along a reaction coordinate there is a molecular orbital crossing. [4] Thus for the butadiene to cyclobutene conversion, the two Möbius (here conrotatory) and Hückel (here disrotatory) modes are shown in Figure 5.

  9. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    In the chemical structures above, the small blue numbers in the structure images are the numbering of the atoms in the main backbone chain of the molecules. Other organic compounds have the formula C 4 H 8 , namely cyclobutane and methylcyclopropane , but are not alkenes and do not fall under the name butene .