Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 218
... Alcohol By R. V. M. Campbell , L. CROMBIE , * and G. PATTENDEN [ Departments of Chemistry , The University of Nottingham , NG7 2RD , and University College ( University of Wales ) , Cardiff ] F presqualene alcohol † had the same mass ...
... Alcohol By R. V. M. Campbell , L. CROMBIE , * and G. PATTENDEN [ Departments of Chemistry , The University of Nottingham , NG7 2RD , and University College ( University of Wales ) , Cardiff ] F presqualene alcohol † had the same mass ...
Page 330
... alcohol , acetone , or acetonitrile , the reaction was still slow giving octa - 1,3,7 - triene as the major product , with a small amount of octadienols . We now report that the reaction of butadiene with water yields octa - 2,7 - dien ...
... alcohol , acetone , or acetonitrile , the reaction was still slow giving octa - 1,3,7 - triene as the major product , with a small amount of octadienols . We now report that the reaction of butadiene with water yields octa - 2,7 - dien ...
Page 355
... alcohol concentration . The varia- tion of k with alcohol concentration in acetone solution was somewhat greater ( 30 % over a ten - fold range ) but there was no full kinetic order in alcohol . The reaction rate and activation ...
... alcohol concentration . The varia- tion of k with alcohol concentration in acetone solution was somewhat greater ( 30 % over a ten - fold range ) but there was no full kinetic order in alcohol . The reaction rate and activation ...
Contents
Page | 1 |
Electrochemical Indications of New Oxidation States in Transitionmetal Dicarbollide Complexes | 8 |
Synthesis of a 1026Pyridinophane by U K GEORGI and J RÉTEY | 32 |
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acetate acid addition alcohol Amer analysis appears aromatic assigned atoms band bond calculated carbon carbonyl Chem Chemical Chemistry chloride chromatography co-ordination Comm complexes compounds concentration configuration confirmed consistent constants containing corresponding coupling Crystal Department of Chemistry derivatives determined effect electron ester ether evidence expected experiments Figure followed formation formed gave give hydrogen indicate intermediate involving isolated ligand mass measured mechanism metal method methyl mixture molecular molecule n.m.r. spectrum nitrogen observed obtained occurs oxidation oxygen peak position possible prepared presence protons radical ratio reaction rearrangement Received recently reduction relative reported Research resonance respectively ring Scheme shift shown shows signals similar solution solvent space group spectra spectrum structure studies substituted suggested Summary synthesis Table temperature Tetrahedron Letters thank tion University values X-ray yield