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  2. 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 ...

  3. Baird's rule - Wikipedia

    en.wikipedia.org/wiki/Baird's_rule

    [1] [2] 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).

  4. 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 ...

  5. Cyclooctadecanonaene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadecanonaene

    Notably, [18]annulene is the first annulene after benzene ([6]annulene) to be fully aromatic: its π-system contains 4n + 2 electrons (n = 4), and it is large enough to comfortably accommodate six hydrogen atoms in its interior, allowing it to adopt a planar shape, thus satisfying Hückel's rule. The discovery of aromatic stabilization for [18 ...

  6. 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.

  7. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    Many simple aromatic rings have trivial names. They are usually found as substructures of more complex molecules ("substituted aromatics"). Typical simple aromatic compounds are benzene, indole, and pyridine. [1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur.

  8. Fed officials say they won't be rushed amid the Trump tariff ...

    www.aol.com/finance/fed-officials-wont-rushed...

    On a month-over-month basis, "core" PCE rose 0.2%, faster than the 0.1% seen in November. Now some Fed watchers are concerned that the tariff talk could dial back any hope of rate cuts in 2025.

  9. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    The cyclobutadienide (2−) ion, however, is aromatic (6 electrons). An atom in an aromatic system can have other electrons that are not part of the system, and are therefore ignored for the 4n + 2 rule. In furan, the oxygen atom is sp² hybridized. One lone pair is in the π system and the other in the plane of the ring (analogous to C-H bond ...