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  2. Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Antiaromaticity

    However, the cyclopropenyl anion has 4 π electrons in a cyclic system and in fact has a substantially higher pK a than 1-propene because it is antiaromatic and thus destabilized. [3] Because antiaromatic compounds are often short-lived and difficult to work with experimentally, antiaromatic destabilization energy is often modeled by simulation ...

  3. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    The cyclopentadienyl anion (C 5 H – 5) with six π electrons is planar and readily generated from the unusually acidic cyclopentadiene (pK a 16), while the corresponding cation with four π electrons is destabilized, being harder to generate than a typical acyclic pentadienyl cations and is thought to be antiaromatic. [8] Similarly, the ...

  4. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone .

  5. Möbius aromaticity - Wikipedia

    en.wikipedia.org/wiki/Möbius_aromaticity

    In contrast to the rarity of Möbius aromatic ground state molecular systems, there are many examples of pericyclic transition states that exhibit Möbius aromaticity. The classification of a pericyclic transition state as either Möbius or Hückel topology determines whether 4N or 4N + 2 electrons are required to make the transition state aromatic or antiaromatic, and therefore, allowed or ...

  6. Homoaromaticity - Wikipedia

    en.wikipedia.org/wiki/Homoaromaticity

    Homoaromaticity, in organic chemistry, refers to a special case of aromaticity in which conjugation is interrupted by a single sp 3 hybridized carbon atom. Although this sp 3 center disrupts the continuous overlap of p-orbitals, traditionally thought to be a requirement for aromaticity, considerable thermodynamic stability and many of the spectroscopic, magnetic, and chemical properties ...

  7. Baird's rule - Wikipedia

    en.wikipedia.org/wiki/Baird's_rule

    The lowest triplet state of an annulene is, according to Baird's rule, aromatic when it has 4n π-electrons and antiaromatic when the π-electron count is 4n + 2, where n is any positive integer. This trend is opposite to that predicted by Hückel's rule for the ground state , which is usually the lowest singlet state (S 0 ).

  8. Booze companies are betting big on nonalcoholic drinks. Here ...

    www.aol.com/alcohol-companies-bracing-culture...

    Major alcohol companies have been bracing for a culture shift favoring nonalcoholic options. Consumers under 30 tend to buy less alcohol and drink less often.

  9. Talk:Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Talk:Antiaromaticity

    3 Cyclopropenyl anion. 2 comments. 4 Peer review and responses during the educational assignment in Fall 2013. 5 Peer Review 1. 1 comment Toggle Peer Review 1 subsection.