Quarterly Journal of the Chemical Society of London |
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Page 24
... addition of a further 2 c.c. of acetic acid and 3 c.c. of water , including any water or acetic acid added with the poison or with the detoxicant . This amount of carbon disulphide was sufficient , while in its normal toxic state , to ...
... addition of a further 2 c.c. of acetic acid and 3 c.c. of water , including any water or acetic acid added with the poison or with the detoxicant . This amount of carbon disulphide was sufficient , while in its normal toxic state , to ...
Page 25
... addition ( as reagent ) being made at room temperature and the remaining additions ( hydrogen peroxide alone ) at 80-85 ° without intermediate cooling . Complete detoxication was reached at a somewhat higher hydrogen peroxide content ...
... addition ( as reagent ) being made at room temperature and the remaining additions ( hydrogen peroxide alone ) at 80-85 ° without intermediate cooling . Complete detoxication was reached at a somewhat higher hydrogen peroxide content ...
Page 47
... addition could conceivably occur at either the ethylenic or acetylenic linkages ; the light absorption of the adducts shows , however , addition at the triple bond as indicated below . This point has been NHRR . Me - CH : CH.CO.CCH ...
... addition could conceivably occur at either the ethylenic or acetylenic linkages ; the light absorption of the adducts shows , however , addition at the triple bond as indicated below . This point has been NHRR . Me - CH : CH.CO.CCH ...
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