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  2. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    In fact, all cyclic conjugated hydrocarbons with a total of 4n π-electrons share this molecular orbital pattern, and this forms the basis of Hückel's rule. Dewar reactivity numbers deriving from the Hückel approach correctly predict the reactivity of aromatic systems with nucleophiles and electrophiles .

  3. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    Hückel's rule is not valid for many compounds containing more than one ring. For example, pyrene and trans-bicalicene contain 16 conjugated electrons (8 bonds), and coronene contains 24 conjugated electrons (12 bonds). Both of these polycyclic molecules are aromatic, even though they fail the 4n + 2 rule. Indeed, Hückel's rule can only be ...

  4. Debye–Hückel theory - Wikipedia

    en.wikipedia.org/wiki/Debye–Hückel_theory

    The Debye–Hückel theory was proposed by Peter Debye and Erich Hückel as a theoretical explanation for departures from ideality in solutions of electrolytes and plasmas. [1] It is a linearized Poisson–Boltzmann model, which assumes an extremely simplified model of electrolyte solution but nevertheless gave accurate predictions of mean activity coefficients for ions in dilute solution.

  5. Möbius–Hückel concept - Wikipedia

    en.wikipedia.org/wiki/Möbius–Hückel_concept

    It is seen that with one MO at the bottom and then groups of degenerate pairs, the Hückel systems will accommodate 4n + 2 electrons, following the ordinary Hückel rule. However, in contrast, the Möbius Systems have degenerate pairs of molecular orbitals starting at the circle bottom and thus will accommodate 4 n electrons.

  6. Extended Hückel method - Wikipedia

    en.wikipedia.org/wiki/Extended_Hückel_method

    The extended Hückel method is a semiempirical quantum chemistry method, developed by Roald Hoffmann since 1963. [1] It is based on the Hückel method but, while the original Hückel method only considers pi orbitals, the extended method also includes the sigma orbitals.

  7. 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 ...

  8. New Year's resolutions for pet owners to make (and keep!) in 2025

    www.aol.com/years-resolutions-pet-owners-keep...

    It’s never too old to teach your pet a new hobby (or trick). For example, if you have a dog breed that’s made for running, like an aerodynamic sighthound or an energetic springer spaniel, the ...

  9. Erich Hückel - Wikipedia

    en.wikipedia.org/wiki/Erich_Hückel

    The famous Hückel 4n+2 rule for determining whether ring molecules composed of C=C bonds would show aromatic properties was first stated clearly by Doering in a 1951 article on tropolone. [6] Tropolone had been recognised as an aromatic molecule by Dewar in 1945. In 1936, Hückel developed the theory of π-conjugated biradicals (non-Kekulé ...