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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 ...

  3. 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]

  4. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    In organic chemistry, a cycloalkene or cycloolefin is a type of alkene hydrocarbon which contains a closed ring of carbon atoms and either one or more double bonds, but has no aromatic character. Some cycloalkenes, such as cyclobutene and cyclopentene , can be used as monomers to produce polymer chains. [ 1 ]

  5. Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Antiaromaticity

    For example, the aromatic species 1 can be reduced to 2 with a relatively small penalty for forming an antiaromatic system. The antiaromatic 2 does revert to the aromatic species 1 over time by reacting with oxygen in the air because the aromaticity is preferred. [15] The loss of antiaromaticity can sometimes be the driving force of a reaction.

  6. Benzocyclobutene - Wikipedia

    en.wikipedia.org/wiki/Benzocyclobutene

    Benzocyclobutene is a strained system which, upon heating to approximately 180 °C, causes the cyclobutene to undergo a conrotatory ring-opening reaction, forming o-xylylene. Since this process destroys the aromaticity of the benzene ring, the reverse reaction is highly favored. Thermal generation of o-xylylene from benzocyclobutene

  7. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    The four carbon atoms in cyclobutane are not coplanar; instead, the ring typically adopts a folded or "puckered" conformation. [2] This implies that the C-C-C angle is less than 90°. One of the carbon atoms makes a 25° angle with the plane formed by the other three carbons. In this way, some of the eclipsing interactions are reduced. The ...

  8. Frontier molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Frontier_molecular_orbital...

    In the conrotatory ring opening of cyclobutene, there are two electrons moving suprafacially (on the pi bond) and two moving antarafacially (on the sigma bond). This means there is one 4 q + 2 suprafacial system and no 4r antarafacial system; thus, the conrotatory process is thermally allowed by the Woodward–Hoffmann rules.

  9. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    Butene, also known as butylene, is an alkene with the formula C 4 H 8.The word butene may refer to any of the individual compounds. They are colourless gases that are present in crude oil as a minor constituent in quantities that are too small for viable extraction.