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  2. Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Antiaromaticity

    An antiaromatic compound may demonstrate its antiaromaticity both kinetically and thermodynamically. As will be discussed later, antiaromatic compounds experience exceptionally high chemical reactivity (being highly reactive is not “indicative” of an antiaromatic compound, it merely suggests that the compound could be antiaromatic).

  3. 1,4-Dioxin - Wikipedia

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

    1,4-Dioxin (also referred as dioxin or p-dioxin) is a heterocyclic, organic, non-aromatic [2] compound with the chemical formula C 4 H 4 O 2.There is an isomeric form of 1,4-dioxin, 1,2-dioxin (or o-dioxin). 1,2-Dioxin is very unstable due to its peroxide-like characteristics.

  4. Borole - Wikipedia

    en.wikipedia.org/wiki/Borole

    The reaction with the electron-poor alkyne (C 6 F 5)CC(C 6 F 5) required rather harsh reaction conditions (110 °C, 7 days) and the only observable species was the expected Diels–Alder product (3), whose formation presumably follows a mechanism similar to that proposed for 5. The same pathway was found for the more electron-rich Et–CC–Et ...

  5. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical reaction occurs. [1] A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction. The detailed steps of a reaction are not observable in most cases.

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    These reactions primarily form cyclopentenones, a cycloalkene that contains two functional groups: the cyclopentene and a ketone group. [12] However, other cycloalkenes, such as Cyclooctatetraene, can be formed as a result of this reaction. [11] Formation of a cyclohexane from a non-cyclic compound via a Cyclization Reaction

  7. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    Two different resonance forms of benzene (top) combine to produce an average structure (bottom). In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone.

  8. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    A chemical reaction is a process that leads to the chemical transformation of one set of chemical substances to another. [1] When chemical reactions occur, the atoms are rearranged and the reaction is accompanied by an energy change as new products are generated.

  9. Chemical compound - Wikipedia

    en.wikipedia.org/wiki/Chemical_compound

    A compound can be converted to a different chemical composition by interaction with a second chemical compound via a chemical reaction. In this process, bonds between atoms are broken in both of the interacting compounds, and then bonds are reformed so that new associations are made between atoms.

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