Journal of the Chemical Society, Part 5Chemical Society., 1949 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 98
Page 14
... alcohol for 5 minutes . The methyl ester forms faintly yellow needles from methyl alcohol , m . p . 201-202 ° ( Found : C , 61.5 ; H , 4.4 . C12H10Os requires C , 61-5 ; H , 4.3 % ) . The ethyl ester was obtained as thin , rhombic ...
... alcohol for 5 minutes . The methyl ester forms faintly yellow needles from methyl alcohol , m . p . 201-202 ° ( Found : C , 61.5 ; H , 4.4 . C12H10Os requires C , 61-5 ; H , 4.3 % ) . The ethyl ester was obtained as thin , rhombic ...
Page 24
... alcohol [ or ether , compare ( VI ) and ( VII ) ] radicals , and take the sequence of reactions ( 1 ) , ( 2 ) , ( 3 ) ... alcohol concentrations the consumption ratio A [ Fe ++ ] / A [ R - H ] should approach an upper limit , and ( ii ) ...
... alcohol [ or ether , compare ( VI ) and ( VII ) ] radicals , and take the sequence of reactions ( 1 ) , ( 2 ) , ( 3 ) ... alcohol concentrations the consumption ratio A [ Fe ++ ] / A [ R - H ] should approach an upper limit , and ( ii ) ...
Page 119
... alcohol - ethyl acetate , m . p . 162-163 ° ( Found : N , 8-3 ; I , 37-5 . C1H1 , N , I requires N , 8.2 ; I , 37.4 % ) , was obtained ( 66 % ) similarly . The dimeth- iodide ( XIIa ) , lustrous orange - yellow plates from aqueous alcohol ...
... alcohol - ethyl acetate , m . p . 162-163 ° ( Found : N , 8-3 ; I , 37-5 . C1H1 , N , I requires N , 8.2 ; I , 37.4 % ) , was obtained ( 66 % ) similarly . The dimeth- iodide ( XIIa ) , lustrous orange - yellow plates from aqueous alcohol ...
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absorption acetic acid acetone activity added alkali aluminium aluminium chloride Amer anhydride aqueous solution aspergillic atom benzene bromide Calc carbon Chem chemical chloroform coefficient colourless complex compounds concentration condensation containing cooled counter crystallised crystals curve decomp decomposition derivatives determined diffusion dilute dinitrogen tetroxide dioxide dissolved distilled dried electrons energy ester ethanol ether ethyl alcohol evaporated experimental experiments extracted filtered formation formed Found fraction gave give gliotoxin H₂O heated hydrochloric acid hydrogen hydrogen chloride hydrolysis iodide iodine value ionic isotopes ketone light petroleum b. p. liquid measured method mixture molecule needles nitrosyl chloride obtained oxidation perchlorate polonium potassium potassium hydroxide precipitated prepared protoactinium pyridine radioactive reaction refluxed requires residue room temperature salt sample separated sodium hydroxide solid soluble solvent sulphate sulphuric acid synthesis thorium thyroxine tube uranium uranyl nitrate washed yellow yield