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  2. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    For instance, Clar's rule can be used to predict several properties of graphene nanoribbons. [10] Aromatic π-sextets play an important part in the determination of the ground state of open shell biradical-type structures., [4] Clar's rule can rationalize the observed decrease in the bandgap of holey graphenes with increasing size. [11]

  3. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_aromatic...

    According to Clar's rule, [20] the resonance structure of a PAH that has the largest number of disjoint aromatic pi sextets—i.e. benzene-like moieties—is the most important for the characterization of the properties of that PAH. [21] Benzene-substructure resonance analysis for Clar's rule

  4. Criegee rearrangement - Wikipedia

    en.wikipedia.org/wiki/Criegee_rearrangement

    In this organic reaction, a tertiary alcohol is cleaved in an organic oxidation by a peroxyacid to a ketone.The acid used is often p-nitroperoxybenzoic acid because the p-nitrobenzoic acid anion is a good leaving group.

  5. Erich Clar - Wikipedia

    en.wikipedia.org/wiki/Erich_Clar

    Erich Clar (23 August 1902 – 27 March 1987) was an Austrian organic chemist, born in Hřensko, who studied polycyclic aromatic hydrocarbon chemistry. He is considered as the father of that field. [ 1 ]

  6. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    A 1,2-rearrangement is an organic reaction where a substituent moves from one atom to another atom in a chemical compound. In a 1,2 shift the movement involves two adjacent atoms but moves over larger distances are possible. Skeletal isomerization is not normally encountered in the laboratory, but is the basis of large applications in oil ...

  7. Rule Maker? Rule Breaker? The Best Companies are Both - AOL

    www.aol.com/2013/04/05/rule-maker-rule-breaker...

    Joe Tenebruso's "Tier 1 Portfolio" has been beating the market handily since its inception. In this series of interviews, Joe talks about what makes a Tier 1 company and which stocks make the cut.

  8. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    Based on Woodward–Hoffmann rules, the electrocyclic opening of norcaradiene derivatives is a 6-electron disrotatory (π 4 s + σ 2 s), thermally allowed process. ring opening. The norcaradiene-cycloheptatriene equilibrium has been studied extensively. [11] The position of the equilibrium depends upon steric, electronic and conformational ...

  9. Auwers synthesis - Wikipedia

    en.wikipedia.org/wiki/Auwers_synthesis

    The Auwers synthesis is a series of organic reactions forming a flavonol from a coumarone.This reaction was first reported by Karl von Auwers in 1908. [1] [2] [3] [4 ...