Quarterly Journal of the Chemical Society of London, Volume 1 |
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Results 1-3 of 71
Page 75
... indicated at values ( 9 ) 10- + 3 2 2 бо 31 -i = 3,6 i = 1,8 4 7 = 2,7 i = 4,5 FIGURE 5 Solid lines indicate the theoretical values of a , against do for radicals from fluorenone . Experimental values of a for the radical anion in NN ...
... indicated at values ( 9 ) 10- + 3 2 2 бо 31 -i = 3,6 i = 1,8 4 7 = 2,7 i = 4,5 FIGURE 5 Solid lines indicate the theoretical values of a , against do for radicals from fluorenone . Experimental values of a for the radical anion in NN ...
Page 78
... indicate that aon is in fact negative since , particularly in solvents such as toluene , the most stable ... indicate close association with the triethyl- amine . On the other hand , results on the Ph2COH radical in mixed solutions of NN ...
... indicate that aon is in fact negative since , particularly in solvents such as toluene , the most stable ... indicate close association with the triethyl- amine . On the other hand , results on the Ph2COH radical in mixed solutions of NN ...
Page 408
... indicated by R ; when more than one independently variable general substituent is present , R1 , R2 , and R3 should be used ( not R , R1 , R2 , R3 ; or R1 , R2 , and R , which indicate 1 x R and multiples of R thereof ) . ( k ) Often it ...
... indicated by R ; when more than one independently variable general substituent is present , R1 , R2 , and R3 should be used ( not R , R1 , R2 , R3 ; or R1 , R2 , and R , which indicate 1 x R and multiples of R thereof ) . ( k ) Often it ...
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