Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 491
... give theoretically a 10 % solution of diol in this phase on completion of the hydrolysis . Methylphenylsilanediol . This compound , m.p. 85 ° ( from pentane - diethyl ether ) , was prepared in a similar fashion to the preceding one ...
... give theoretically a 10 % solution of diol in this phase on completion of the hydrolysis . Methylphenylsilanediol . This compound , m.p. 85 ° ( from pentane - diethyl ether ) , was prepared in a similar fashion to the preceding one ...
Page 864
... give EA 85.8 kJ mol - 1 , log ( A / s - 1 ) 9.9 . These rate constants give E △ 92.0 kJ mol - 1 , log ( A / s - 1 ) 9.9 . These rate constants give EA 93.7 kJ mol - 1 , log ( A / s - 1 ) 10.6 . Figures in parentheses give = the ...
... give EA 85.8 kJ mol - 1 , log ( A / s - 1 ) 9.9 . These rate constants give E △ 92.0 kJ mol - 1 , log ( A / s - 1 ) 9.9 . These rate constants give EA 93.7 kJ mol - 1 , log ( A / s - 1 ) 10.6 . Figures in parentheses give = the ...
Page 923
... give several extra products . Thus , oxygen inter- cepts the trichloromethyl radical - chain carriers to give phosgene and hydrogen chloride 16 which react further with the secondary amine to form NNN'N ' - tetra- alkylurea and amine ...
... give several extra products . Thus , oxygen inter- cepts the trichloromethyl radical - chain carriers to give phosgene and hydrogen chloride 16 which react further with the secondary amine to form NNN'N ' - tetra- alkylurea and amine ...
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