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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... formed due to oscillation of two static potential energy particles that spreads through waves. Base level hydrogen atoms/God particles are formed in crest & trough region of kinetic energy waves. These God particles are formed above ...
... formed due to oscillation of two static potential energy particles that spreads through waves. Base level hydrogen atoms/God particles are formed in crest & trough region of kinetic energy waves. These God particles are formed above ...
Page 9
... formed . The quartz of the second layer appears , evidently , to have formed its crystalline points ; and these points have caused the third layer of opal or zeolite to assume the botryoidal form . Now , it is not , perhaps , possible ...
... formed . The quartz of the second layer appears , evidently , to have formed its crystalline points ; and these points have caused the third layer of opal or zeolite to assume the botryoidal form . Now , it is not , perhaps , possible ...
Page 36
... formed portion of tap root . The Petri net contains supplementary arcs labelled a , b and c ( broken lines ) . Even when the requisite pre - conditions are fulfilled , these arcs are not always invoked . Each part of the Table therefore ...
... formed portion of tap root . The Petri net contains supplementary arcs labelled a , b and c ( broken lines ) . Even when the requisite pre - conditions are fulfilled , these arcs are not always invoked . Each part of the Table therefore ...
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