Quarterly Journal of the Chemical Society of London, Volume 6 |
From inside the book
Results 1-3 of 75
Page 1071
... shown in Table 1. It is convenient to consider the assignments of the fundamental modes of vibration in terms of particular groupings present in two or more of these esters as shown in Table 2 , which is an extension of the description ...
... shown in Table 1. It is convenient to consider the assignments of the fundamental modes of vibration in terms of particular groupings present in two or more of these esters as shown in Table 2 , which is an extension of the description ...
Page 1469
... shown to possess stereochemical stability dependence on an acidity function will necessitate in the cis - form.26-29 H * + RC = C - CO , H RC = C- CO , H ; + X ^ R K2 . RC = C • CO2H2 k2 R fast C = C H substantial C - H bond formation ...
... shown to possess stereochemical stability dependence on an acidity function will necessitate in the cis - form.26-29 H * + RC = C - CO , H RC = C- CO , H ; + X ^ R K2 . RC = C • CO2H2 k2 R fast C = C H substantial C - H bond formation ...
Page 1636
... shown to be pure by mass spectrometry and gas chromatography ( 1.5 m silica gel at 21 ° ) , was desorbed and estimated by measuring its pressure in a known volume ; this procedure was shown to be accurate to + 1 % with known mixtures ...
... shown to be pure by mass spectrometry and gas chromatography ( 1.5 m silica gel at 21 ° ) , was desorbed and estimated by measuring its pressure in a known volume ; this procedure was shown to be accurate to + 1 % with known mixtures ...
Contents
ISCHA 013 | 1034 |
Physical organic chemistry | 1035 |
Studies of the reactions of the anhydrosulphites of ahydroxycarboxylic acids Part IV Steric | 1044 |
24 other sections not shown
Other editions - View all
Common terms and phrases
absorption acetic acid activation added addition alcohol Amer amine anhydrosulphite anion appears aqueous aromatic assigned atom attack bands base benzene bond buffer calculated carbon carbon tetrachloride Chem chloride compared compounds concentration conformation containing corresponding decomposition derived described determined discussed effect electron energy equation ester ether evidence excess expected experimental experiments factors Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate interaction involving kinetic less measured mechanism method methyl MICHIGAN mixture molecular molecules nitrogen nucleophilic observed obtained occurs organic oxidation phenyl phosphate plot position possible prepared presence proton pyridine radical radical anion rate constants ratio reaction reactivity reduction relative reported requires respectively ring showed shown similar sodium solution solvent spectra spectrum splitting structure studied substituent suggested Table temperature transition University values yield