Quarterly Journal of the Chemical Society of London |
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Page 68
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . MARGARET LE PLA , B.SC. The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new ...
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . MARGARET LE PLA , B.SC. The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new ...
Page 144
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new knowledge in all branches ...
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new knowledge in all branches ...
Page 332
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new knowledge in all branches ...
... Chemical Society was founded in 1841 and received a Royal Charter in 1848 . The main function of the Society is to foster original research in Chemistry and to facilitate the discussion and dissemination of new knowledge in all branches ...
Contents
The Ternary Systems NaSCNCa SCNH₂O KSCNCaSCNH₂O NHSCNCaSCNH₂O | 1 |
Rareearth Metal Oxides | 7 |
The Acetone Derivatives of Hexahydric Alcohols Part I Triacetone Mannitol and its Conversion | 13 |
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Common terms and phrases
3′-pyridoacridine 4-dideuterobenzene absorption acetic acid acetone acridone active added alkali alkyl Amer amidine ammonia atoms bands benzene bimolecular boiling Calc carbinol CH₂ Chem Chemical chloride combination tones compound condensation cooled crude crystallised D.Sc decomp derivative deuterated benzenes deuterium dilute dissolved distilled dried effect ester ether ethyl alcohol experimental extracted filtered formed Found fraction fundamental frequencies gave give b. p. halides heated hexadeuterobenzene hydrochloric acid hydrochloride hydrogen hydrolysis infra-red spectrum Ingold iodide ionisation isolated ketone kg.-cals ligroin methanol method mixture molecule monodeuterobenzene neopentyl neopentyl bromide nitrate normal co-ordinates obtained oxide picrate potassium potassium carbonate praseodymium precipitate prepared prisms pyridine Raman spectrum reaction reagent rearrangement refluxed requires residue salt separated sodium carbonate sodium hydroxide solid soluble solution solvent spectra steric steric effect stirred substitution sulphate sulphuric acid symmetry class Table temperature washed yellow needles yield