Quarterly Journal of the Chemical Society of London, Volume 6 |
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Results 1-3 of 83
Page 1407
... [ equation ( 12 ) ] . * From the slope ( S ) and intercept ( Y ) of equation ( 12 ) , KнА = 540 ( Table 12 ) . This would represent the association constant for acetic ( kí ) -1 = 615 × 103 [ HOAc ] + 332 ( 12 ) n = 3 · 7 × 10-5 ; m ...
... [ equation ( 12 ) ] . * From the slope ( S ) and intercept ( Y ) of equation ( 12 ) , KнА = 540 ( Table 12 ) . This would represent the association constant for acetic ( kí ) -1 = 615 × 103 [ HOAc ] + 332 ( 12 ) n = 3 · 7 × 10-5 ; m ...
Page 1422
... equation ( 5 ) . If a and b are the initial concentrations of the di - imine and phenol , ( 5 ) d [ In ] / dt = k2 [ di - imine ] [ phenol ] and x is the concentration of indoaniline at time t , we get equation ( 6 ) and with the ...
... equation ( 5 ) . If a and b are the initial concentrations of the di - imine and phenol , ( 5 ) d [ In ] / dt = k2 [ di - imine ] [ phenol ] and x is the concentration of indoaniline at time t , we get equation ( 6 ) and with the ...
Page 1461
... equation ( 4 ) or , if equations ( 1 ) , ( 2 ) , and ( 3 ) = 21 ( 2 ) = 1 X2 ( 2 ) ( 4 ) In x = { ( 4-916 - [ 1 + 4-73 ( 7 ) ] } ( 8b ) 505 To As pointed out , the vapour pressure measurements showed that the activity coefficient y ...
... equation ( 4 ) or , if equations ( 1 ) , ( 2 ) , and ( 3 ) = 21 ( 2 ) = 1 X2 ( 2 ) ( 4 ) In x = { ( 4-916 - [ 1 + 4-73 ( 7 ) ] } ( 8b ) 505 To As pointed out , the vapour pressure measurements showed that the activity coefficient y ...
Contents
ISCHA 013 | 1034 |
Physical organic chemistry | 1035 |
Studies of the reactions of the anhydrosulphites of ahydroxycarboxylic acids Part IV Steric | 1044 |
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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