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Pentadienyl radical, resonance energy

The activation energy is only 7 kcal/mol less than that for the vinylcyclopropane rearrangement itself, consistent with roughly 20 kcal/mol for the pentadienyl radical resonance energy, and suggests that the reaction is not concerted. [Pg.193]

D.F. McMiUen and D.M. Golden, Cyclohexadienyl radical resonance energy is 7 kcal/ mol greater than that of the pentadienyl radical from bond dissociation energies, Anna. Rev. Phys. Chem., 33, 493 (1982). [Pg.169]

Sketch the molecular orbitals for the pentadienyl system in order of ascending energy (see Figures 14-2 and 14-7). Indicate how many electrons are present, and in which orbitals, for (a) the radical (b) the cation (c) the anion (see Figures 14-3 and 14-7). Draw all reasonable resonance forms for any one of these three species. [Pg.631]


See other pages where Pentadienyl radical, resonance energy is mentioned: [Pg.276]    [Pg.213]    [Pg.711]    [Pg.4]    [Pg.448]    [Pg.448]    [Pg.704]    [Pg.10]    [Pg.245]    [Pg.10]   
See also in sourсe #XX -- [ Pg.448 ]




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