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  2. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical and physical properties.

  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. Erich Clar - Wikipedia

    en.wikipedia.org/wiki/Erich_Clar

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

  5. Atoms in molecules - Wikipedia

    en.wikipedia.org/wiki/Atoms_in_molecules

    One traditional explanation is given by Clar's rule. QTAIM shows that a calculated stabilization of 8 kcal/mol (33 kJ/mol) for phenanthrene is the result of destabilization of the compound by 8 kcal/mol (33 kJ/mol) originating from electron transfer from carbon to hydrogen, offset by 12.1 kcal (51 kJ/mol) of stabilization due to a H...H bond path.

  6. Corey–Nicolaou macrolactonization - Wikipedia

    en.wikipedia.org/wiki/Corey–Nicolaou...

    The hydroxy acid first reacts with the 2,2'-Dipyridyldisulfide to form the corresponding 2-pyridinethiol ester, and after a proton transfer, the alkoxide attacks the carbonyl carbon, forming a tetrahedral transition state, before resolving back to the desired lactone and 2-pyridinethione.

  7. Cadiot–Chodkiewicz coupling - Wikipedia

    en.wikipedia.org/wiki/Cadiot–Chodkiewicz_coupling

    The Cadiot–Chodkiewicz coupling in organic chemistry is a coupling reaction between a terminal alkyne and a haloalkyne catalyzed by a copper(I) salt such as copper(I) bromide and an amine base.

  8. Arndt–Eistert reaction - Wikipedia

    en.wikipedia.org/wiki/Arndt–Eistert_reaction

    In organic chemistry, the Arndt–Eistert reaction is the conversion of a carboxylic acid to its homologue.It is named for the German chemists Fritz Arndt (1885–1969) and Bernd Eistert (1902–1978).

  9. Balz–Schiemann reaction - Wikipedia

    en.wikipedia.org/wiki/Balz–Schiemann_reaction

    The traditional Balz–Schiemann reaction employs HBF 4 and involves isolation of the diazonium salt. Both aspects can be profitably modified. Other counterions have been used in place of tetrafluoroborates, such as hexafluorophosphates (PF 6 −) and hexafluoroantimonates (SbF 6 −) with improved yields for some substrates.