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  2. Heptalene - Wikipedia

    en.wikipedia.org/wiki/Heptalene

    Heptalene is a polycyclic hydrocarbon with chemical formula C 12 H 10, composed of two fused cycloheptatriene rings. It is an unstable, non-planar compound which is non-aromatic. [1] [2] The dianion, however, satisfies Hückel's rule, is thermally stable, and is planar. [3]

  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 ...

  4. 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, but merely suggests that the compound could be antiaromatic.

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  6. Chemical equation - Wikipedia

    en.wikipedia.org/wiki/Chemical_equation

    A chemical equation is the symbolic representation of a chemical reaction in the form of symbols and chemical formulas.The reactant entities are given on the left-hand side and the product entities are on the right-hand side with a plus sign between the entities in both the reactants and the products, and an arrow that points towards the products to show the direction of the reaction. [1]

  7. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...

  8. Annulene - Wikipedia

    en.wikipedia.org/wiki/Annulene

    The discovery that [18]annulene possesses a number of key properties associated with other aromatic molecules was an important development in the understanding of aromaticity as a chemical concept. In the related annulynes , one double bond is replaced by a triple bond .

  9. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde (/ f ɔːr ˈ m æ l d ɪ h aɪ d / ⓘ for-MAL-di-hide, US also / f ə r-/ ⓘ fər-) (systematic name methanal) is an organic compound with the chemical formula CH 2 O and structure H−CHO, more precisely H 2 C=O. The compound is a pungent, colourless gas that polymerises spontaneously into paraformaldehyde.