Journal of the Chemical SocietyThe Society., 1953 |
From inside the book
Results 1-3 of 75
Page 42
... effect of nitrogen on both limits was summarised on p . 39. The fact that both graphs are linear is consistent with the conclusion that nitrogen behaves entirely as an inert gas . The greater effect of nitrogen on the hydrogen - nitrous ...
... effect of nitrogen on both limits was summarised on p . 39. The fact that both graphs are linear is consistent with the conclusion that nitrogen behaves entirely as an inert gas . The greater effect of nitrogen on the hydrogen - nitrous ...
Page 290
... effect on the melting - point should be suitable for this purpose . Ethyl , propyl , and isopropyl groups are known to exert such an effect , generally in much greater measure than methyl or tert . - butyl groups . The solubilities of ...
... effect on the melting - point should be suitable for this purpose . Ethyl , propyl , and isopropyl groups are known to exert such an effect , generally in much greater measure than methyl or tert . - butyl groups . The solubilities of ...
Page 888
... effect on the velocity of reaction , whereas other salts have a considerable effect in the less aqueous solvents , but no effect in the 33 % aqueous solution . These results are in agreement with the bimolecular S2 mechanism of the ...
... effect on the velocity of reaction , whereas other salts have a considerable effect in the less aqueous solvents , but no effect in the 33 % aqueous solution . These results are in agreement with the bimolecular S2 mechanism of the ...
Contents
Internuclear Cyclisation Part VII The Synthesis of Some NitroNmethyl | 1 |
Synthesis of Polymethylnaphthalenes | 8 |
Kestose a Trisaccharide formed from Sucrose by Yeast Invertase | 24 |
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Common terms and phrases
absorption acetic acid acetic anhydride acetone acetyl acidified added alcohol alkaline aluminium aluminium chloride Amer amine aqueous sodium atom benzene boiling bromine Calc carbon Chem Chim chloroform chromatographed colourless compound concentrated cooled crystallised crystals D.Sc decomp derivatives dilute dissolved distilled dried elution equiv ester ethanol ethyl acetate ethylene evaporated extracted with ether filtered filtrate formed Found fraction gave give m. p. H₂O heated hydrochloric acid hydrogen chloride hydrogen sulphate hydrolysis hydroxyl infra-red iodide isolated ketone light petroleum b. p. liquid lithium aluminium hydride m. p. and mixed method mixed m. p. mixture mole obtained oxidation oxidised pale yellow phosphorochloridate polyporenic potassium hydroxide precipitate prepared prisms pyridine reaction reduced refluxed requires residue room temperature salt sodium hydroxide solid soluble solution solvent spectra sulphuric acid ultra-violet washed yellow needles yield