Journal of the Chemical SocietyThe Society., 1954 |
From inside the book
Results 1-3 of 78
Page 206
... experiments recovery of acetaldehyde from paraldehyde was 83-8 and 82.8 % ( mean correction factor 0.833 ) . Although the results are not of absolute quantitative significance they show that the groups behave in the expected order . The ...
... experiments recovery of acetaldehyde from paraldehyde was 83-8 and 82.8 % ( mean correction factor 0.833 ) . Although the results are not of absolute quantitative significance they show that the groups behave in the expected order . The ...
Page 224
... experiments of this kind . THIS paper is a sequel to that of Thomas and Staveley ( J. , 1952 , 4569 ) , describing experiments on the supercooling of various molecular liquids . Each liquid was examined as a cloud of small droplets ...
... experiments of this kind . THIS paper is a sequel to that of Thomas and Staveley ( J. , 1952 , 4569 ) , describing experiments on the supercooling of various molecular liquids . Each liquid was examined as a cloud of small droplets ...
Page 363
... experiments the catalyst concentration was nearly the same . Each group of experiments in Table 1 is a series performed with catalyst solutions derived from the same sample of stannic chloride . Between each series of experiments , the ...
... experiments the catalyst concentration was nearly the same . Each group of experiments in Table 1 is a series performed with catalyst solutions derived from the same sample of stannic chloride . Between each series of experiments , the ...
Contents
Organic | xv |
Magnetic Moments and Stereochemistry of Cobaltous Compounds | xv |
789Tetrahydro4 7sulphinylthionaphthen | 15 |
136 other sections not shown
Other editions - View all
Common terms and phrases
absorption spectra acetic acid acetic anhydride acetone acetyl added addition alcohol alkaline alumina aluminium Amer amine ammonia aqueous atom band benzaldehyde benzene boiling bond bromide Calc carbonate carbonyl Chem chloride chloroform chromatography colour colourless complexes compound concentrated cooled crystallised crystals cyanogen cyanogen chloride decomp derivatives diazotised dilute dissolved distilled dried eluted equiv ester ether evaporated extracted ferric filtered formed Found fraction gave give H₂O heated hydrobromic acid hydrochloric acid hydrogen hydrogen chloride hydrolysis infra-red isolated ketone ligand light petroleum b. p. liquid m. p. and mixed methanol methyl mixed m. p. mixture molecule needles nitrate obtained orbitals oxidation phenol phosphate potassium hydroxide precipitate prepared pyridine reaction refluxed Reprint Order requires residue room temperature salt separated sodium carbonate sodium hydroxide solid solution solvent spectrum stirring sulphate sulphide sulphone sulphuric acid Table washed yield