Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 155
... assumed orientation of component 2 and calculate a value for ( T2 ) m which is less than the value of г at any con- centration , we know at once that our assumed orienta- tion is incorrect or that the thickness of the adsorbed phase in ...
... assumed orientation of component 2 and calculate a value for ( T2 ) m which is less than the value of г at any con- centration , we know at once that our assumed orienta- tion is incorrect or that the thickness of the adsorbed phase in ...
Page 690
... Assumed 0 5.0 × 1010 d 0 1.0 x 1010 7b 10.0 Estimated as for 3 Assumed same as Estimated - 3 from similar reactions ; 15 , 16 Assumed Units : A and k in sec . - 1 , mole - 1 1. sec . - 1 , or mole - 2 1.2 sec . - 1 ; E in cal . mole - 1 ...
... Assumed 0 5.0 × 1010 d 0 1.0 x 1010 7b 10.0 Estimated as for 3 Assumed same as Estimated - 3 from similar reactions ; 15 , 16 Assumed Units : A and k in sec . - 1 , mole - 1 1. sec . - 1 , or mole - 2 1.2 sec . - 1 ; E in cal . mole - 1 ...
Page 956
... assumed that the A values of unsubstituted hydrocarbons represent the latter contribution , while the difference in A between substituted and unsubstituted species ( substituent solvent shift ) corresponds to the former contribution ...
... assumed that the A values of unsubstituted hydrocarbons represent the latter contribution , while the difference in A between substituted and unsubstituted species ( substituent solvent shift ) corresponds to the former contribution ...
Contents
Physical organic chemistry | 1 |
Topochemistry Part XXX Crystal and molecular structures of chalcone | 11 |
Conformational studies Part I Crystal and molecular structures of cis12dipchlorobenzoyl and cis | 17 |
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acetic acid activation added addition alcohol Amer angle appears aqueous assumed ation atoms base benzene bond bromination calculated carbon carbon tetrachloride Chem chemical Chemistry chloride compared complex compounds concentration conformation containing corresponding coupling crystal dependence derivatives determined difference DISCUSSION effect elimination energy equation error estimated ethanol ether exchange expected experimental experiments Figure formation fraction give given hydrogen increase indicators interaction intermediate involving isomer isotope kinetic measured mechanism method methyl mixture mole molecular molecule observed obtained occurs oxide oxygen parameters Phys plot position possible prepared present proton radical range rate constants ratio reaction reasonable relative reported requires respectively ring shifts shown shows similar sodium solution solvent spectra spectrum structure substituents suggested sulphuric Table temperature transition University values wave yield