Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 1549
... compounds would not be ] , and closely resemble those of the appropriate Me , Si CH , CH2 SiMe , compounds . 4 ( b ) The proton magnetic resonance spectra of the m- and p - Сl · С ̧H1 · CH ̧ • SiMeg derivatives of the addition products ...
... compounds would not be ] , and closely resemble those of the appropriate Me , Si CH , CH2 SiMe , compounds . 4 ( b ) The proton magnetic resonance spectra of the m- and p - Сl · С ̧H1 · CH ̧ • SiMeg derivatives of the addition products ...
Page 1816
... compound ) . Indirect evidence for the square - pyramidal structure for our cobalt compounds ( V ) is that their electron spin resonance spectra indicate that they are paramagnetic , like compound ( VII ) , and their infrared spectra ...
... compound ) . Indirect evidence for the square - pyramidal structure for our cobalt compounds ( V ) is that their electron spin resonance spectra indicate that they are paramagnetic , like compound ( VII ) , and their infrared spectra ...
Page 1820
... compounds ( I ; M = Cu , X = Cl or Br ) when treated in cold chloroform solution with chlorine and bromine , respectively , appeared to undergo general decomposition , and the corresponding copper ( II ) compounds cannot be obtained in ...
... compounds ( I ; M = Cu , X = Cl or Br ) when treated in cold chloroform solution with chlorine and bromine , respectively , appeared to undergo general decomposition , and the corresponding copper ( II ) compounds cannot be obtained in ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
57 other sections not shown
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1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield