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Page 3879
... iodide : 3IC1 + 3KI → 3KCl + 312 ( 3 ) In titration C , therefore , a certain amount of iodic acid must have been directly reduced to iodine according to ( 2 ) , the remainder undergoing stepwise reduction according to ( 1 ) and ( 3 ) ...
... iodide : 3IC1 + 3KI → 3KCl + 312 ( 3 ) In titration C , therefore , a certain amount of iodic acid must have been directly reduced to iodine according to ( 2 ) , the remainder undergoing stepwise reduction according to ( 1 ) and ( 3 ) ...
Page 3885
... iodide had been added . Had iodine tribromide been formed and it underwent no hydrolysis , the pH curve ( 3 ) would have been inflected with 1 mols . of iodide . It might be thought that as the redox curve ( 1 ) is inflected with 1.35 ...
... iodide had been added . Had iodine tribromide been formed and it underwent no hydrolysis , the pH curve ( 3 ) would have been inflected with 1 mols . of iodide . It might be thought that as the redox curve ( 1 ) is inflected with 1.35 ...
Page 3891
... iodide , and therefore for the completion of reaction ( 2 ) and the subsequent formation of 1 mol . of iodine bromide ( 4 ) , a total of 1 mol . of iodide were required to bring each of the curves " 2 , " " 5 , " and 10 " in Fig . 1 to ...
... iodide , and therefore for the completion of reaction ( 2 ) and the subsequent formation of 1 mol . of iodine bromide ( 4 ) , a total of 1 mol . of iodide were required to bring each of the curves " 2 , " " 5 , " and 10 " in Fig . 1 to ...
Contents
ONE HUNDRED AND ELEVENTH ANNUAL GENERAL MEETING | 2449 |
483 | 2465 |
Mechanism of Substitution at a Saturated Carbon Atom Part XXXIII Kinetic | 2488 |
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acetic acid acetone acetyl acetyl chloride added alcohol alum aluminium aluminium bromide Amer ammonia anhydride aqueous atom benzene benzyl boiling Calc carbon Chem Chemical Chemistry chloroform chromatography colourless compound concentrated condensation cooled crystallised crystals decomp derivative dilute dissolved distilled dried ester ethanol ether ethyl acetate ethylene evaporated excess extracted filtered filtrate formed Found fraction gave give heated hydrate hydrochloric acid hydrogen bromide hydrogen chloride hydrolysis iodide isolated ketone L-iditol Lecture light petroleum b. p. lignin lithium aluminium hydride m. p. and mixed material method methyl mixed m. p. mixture molecular molecules needles nitrate obtained oxide phase phosphate polymer potassium hydroxide precipitated prepared present Professor pyridine reaction reflux requires residue retinene room temperature salt sample separated sodium hydroxide solid solution solvent stirred structure Table trifluoroiodomethane vapour pressure vitamin washed yellow yield