Journal of the Chemical SocietyThe Society., 1948 |
From inside the book
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Page 31
... corresponding to the presence of one non - reducing terminal residue per 500 100 glucose residues after allowing for formic acid produced by the amylopectin fraction ( 10 % ) and by the reducing end of the amylose molecule . Rice Starch ...
... corresponding to the presence of one non - reducing terminal residue per 500 100 glucose residues after allowing for formic acid produced by the amylopectin fraction ( 10 % ) and by the reducing end of the amylose molecule . Rice Starch ...
Page 148
... corresponding sulphonamides but gave mainly water- soluble products , which probably consisted of salts of the corresponding sulphonic acids , and in some cases the disulphone . According to Otto and Ostrop ( Annalen , 1867 , 141 , 372 ) ...
... corresponding sulphonamides but gave mainly water- soluble products , which probably consisted of salts of the corresponding sulphonic acids , and in some cases the disulphone . According to Otto and Ostrop ( Annalen , 1867 , 141 , 372 ) ...
Page 282
... corresponding amine , which could not be converted into 4 ' - amino - 2 ′ : 5 ′ - dimethoxy - 3 - phenyl - 4 - methyl phthalaz- 1 - one by the usual methods . The latter , however , was readily obtained by reducing the corresponding ...
... corresponding amine , which could not be converted into 4 ' - amino - 2 ′ : 5 ′ - dimethoxy - 3 - phenyl - 4 - methyl phthalaz- 1 - one by the usual methods . The latter , however , was readily obtained by reducing the corresponding ...
Contents
kilocals as the free energy difference contributed by the hyperconjugated methyl group | 373 |
SIR WILLIAM RAMSAY AND Ralph Forster LABORATORIES | 417 |
control of anionotropic rearrangement and of the significance of conjugation and hypercon | 440 |
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Common terms and phrases
4-dideuterobenzene absorption spectrum acetic acid acetic anhydride acetone added alkaline Amer ammonia analcite aqueous sodium atoms bands benzene boiling bond bromine Calc carbon catalyst CH₂ chabazite Chem chloride chloroform colourless needles compound concentrated cooled corresponding crystallised from alcohol crystals cyanide D.Sc decomp derivative dilute dissolved distilled dried electronic origin energy ester ethanol ether evaporated excited extracted filtered filtrate fluorescence formed Found fraction fundamental frequencies gave give H₂O heated hexadeuterobenzene hydrochloric acid hydrogen hydrogen chloride hydrolysis Ingold isolated kcals ketone light petroleum method methyl alcohol mixed m. p. mixture molecule obtained oxidation peroxide phenol potassium potassium hydroxide precipitated prepared prisms pyridine reaction reduced pressure refluxed requires residue room temperature salt separated sodium hydroxide solid soluble solution solvent spectra structure sulphide sulphuric acid symmetry transitions unsaturated upper electronic upper-state vibration washed yellow needles yield