Journal of the Chemical Society, Part 3, Pages 2489-3512The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 2904
... molecule . " The ionisation energy of a localised bond is compared with the ionis- ation energies of the valence atomic orbitals of the " atom in the molecule " to show that the electron is more tightly bound in the bond than in the ...
... molecule . " The ionisation energy of a localised bond is compared with the ionis- ation energies of the valence atomic orbitals of the " atom in the molecule " to show that the electron is more tightly bound in the bond than in the ...
Page 2906
... molecule to molecule and this shows again that the lone pairs do exist effectively unchanged in different molecules . There does not seem to be any general connection between the ionisation energy and either the hybridisation in the ...
... molecule to molecule and this shows again that the lone pairs do exist effectively unchanged in different molecules . There does not seem to be any general connection between the ionisation energy and either the hybridisation in the ...
Page 2919
... molecule and if there are hybrid atomic orbitals in the molecule , then the atomic orbitals of ( 10 ) must be hybridised in the same way . It is assumed that the molecule is electrically neutral and that the atomisation is to neutral ...
... molecule and if there are hybrid atomic orbitals in the molecule , then the atomic orbitals of ( 10 ) must be hybridised in the same way . It is assumed that the molecule is electrically neutral and that the atomisation is to neutral ...
Contents
Fluorocarbohydrates Part VIII Formation of halogenoderivatives from | 2493 |
Steric influences in radical reactions Part I Benzyl radicals derived from cyclic | 2500 |
56dioisopropylidene | 2514 |
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absorption acetic acid acetone added adduct alcohol Amax Amer aqueous aromatic ation atom atomic orbitals band benzene bond bromide Calc carbon carbonyl CH₂ Chem chloroform chromatography cm.¹ complex compound concentrated cooled crystallised cyclic cyclohexane decomp decomposition dilute dioxide distilled dried electron elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate formation formed Found fraction gave give heated hydrochloric hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum ionisation energies isolated isomer ketone kinetic light petroleum mechanism methyl mixed m. p. mixture mole molecular molecule nitrate nitric nitric oxide nitrogen Nujol obtained oxide oxime perchlorate petroleum b. p. polymer potassium potassium hydroxide prepared proton pyridine reaction rearrangement reduced refluxed requires residue room temperature salt sodium solid solution solvent spectra structure sulphuric acid Table thionyl chloride transition ultraviolet values Vmax yellow yield