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Electron diffraction Electronegativity

There is evidence from electron diffraction studies of pyrazine and pyridine that this value should be increased by 0.01 or 0.02 A because of the electronegativity of nitrogen (V. Schomaker and L. Pauling, paper to be published in Jour. Am. Chem. Soc.). [Pg.226]

Electron-deficient olefins, asymmetric epoxidation, 386-91 Electron diffraction dialkyl peroxides, 713 ozonides, 721, 723 1,2,4-trioxolanes, 740 see also Gas electron diffraction Electron-donating substituents ene reactions, 841 sulfonyl peroxides, 1005-7 Electronegative functional groups,... [Pg.1458]

In the boron trimethyl molecule the boron atom is surrounded by three pairs of valence electrons, which are involved in the formation of single covalent bonds to the three carbon atoms of the methyl groups. An electron-diffraction study10 has shown the molecule to be planar (except for the hydrogen atoms), as would be expected for sp1 hybrid orbitals. The —C distance is 1.56 i 0.02 A, which agrees reasonably well with the value 1.54 A calculated, with the electronegativity correction, by the use of 0.81 A for the boron single-bond radius.11... [Pg.317]


See other pages where Electron diffraction Electronegativity is mentioned: [Pg.47]    [Pg.666]    [Pg.850]    [Pg.47]    [Pg.363]    [Pg.990]    [Pg.468]    [Pg.181]    [Pg.809]    [Pg.49]    [Pg.87]    [Pg.36]    [Pg.240]    [Pg.511]    [Pg.152]    [Pg.177]    [Pg.520]    [Pg.152]    [Pg.177]    [Pg.15]    [Pg.269]    [Pg.368]    [Pg.19]    [Pg.203]    [Pg.244]    [Pg.485]    [Pg.37]    [Pg.561]   
See also in sourсe #XX -- [ Pg.262 , Pg.262 ]




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Electron diffraction

Electronic diffraction

Electrons diffracted

Electrons electronegativity

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