Quarterly Journal of the Chemical Society of London |
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Page 2956
... Preparation of Esters of Alkyl- and Aryl - boronic Acids . By P. B. BRINDLEY , W. GERRARD , and M. F. LAPPERT . [ Reprint Order No. 6303. ] Di - n - butyl boronate was prepared from n - butylmagnesium bromide ( 1 mol . ) , or , in ...
... Preparation of Esters of Alkyl- and Aryl - boronic Acids . By P. B. BRINDLEY , W. GERRARD , and M. F. LAPPERT . [ Reprint Order No. 6303. ] Di - n - butyl boronate was prepared from n - butylmagnesium bromide ( 1 mol . ) , or , in ...
Page 3056
... prepared by crystallisation from or by precipitation ( on addition of ethyl alcohol ) from aqueous solutions of hydrogen peroxide and the corresponding sulphate or selenate Na , SO1 , 0 · 5H2O ,, H2O ; ( NH ) , SO ,, H , O ,; Na , SeO 4 ...
... prepared by crystallisation from or by precipitation ( on addition of ethyl alcohol ) from aqueous solutions of hydrogen peroxide and the corresponding sulphate or selenate Na , SO1 , 0 · 5H2O ,, H2O ; ( NH ) , SO ,, H , O ,; Na , SeO 4 ...
Page 3169
... prepared by Phillips's method ( J. , 1925 , 2553 ) , and distilled in a high vacuum . Sulphinyl chlorides were prepared by Hilditch and Smiles's method ( Ber . , 1908 , 41 , 4113 ) . Deuterated sulphinic acids were prepared by ...
... prepared by Phillips's method ( J. , 1925 , 2553 ) , and distilled in a high vacuum . Sulphinyl chlorides were prepared by Hilditch and Smiles's method ( Ber . , 1908 , 41 , 4113 ) . Deuterated sulphinic acids were prepared by ...
Contents
2 4Trimethylpentane | 2082 |
Cinnolines Part XXXIV 5 6 and 7Hydroxy and 5 6 and 7Aminocinnolines | 2100 |
The Conductometric Evaluation of the Ionisation Functions of the Monohalogenoacetic | 2104 |
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absorption acetic anhydride acetone acetyl added alcohol alkaline Amer ammonia atom band benzene boiling bromine Calc carbon carbonyl Chem chloride chloroform colour colourless compound concentrated cooled crystallised crystals decomp derivative diethyl dilute dioxide dissolved distilled dried eluted ester ethanol ethylene evaporated filtered fluoride formed Found fraction gave give glacial acetic acid H₂O heated hydrochloric acid hydrogen hydrogen bromide hydrogen chloride hydrolysis infrared isolated ketone lanthanons light petroleum b. p. liquid lithium aluminium hydride m. p. and mixed method methyl mixed m. p. mixture mole needles nickel nitrate nitric nitryl fluoride obtained oxidation oxygen peroxide potassium hydroxide precipitate prepared pressure prisms pteridine pyridine reaction reduction refluxed Reprint Order requires residue resin room temperature sodium hydroxide solid soluble solution solvent spectra spectrum structure sulphuric acid Table tube ultraviolet vacuo washed yellow yield