Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 63
... obtained was distilled under reduced pressure to give 2 - phenylazobenzene ( 89 % ) as a red oil , b.p. 160-162 ° / 1 nm . , which solidified to a red solid , m.p. 38-39 ° ( lit. , m.p. 37-39 ° ) ( Found : C , 83.65 ; H , 5 · 4 ; N , 10 ...
... obtained was distilled under reduced pressure to give 2 - phenylazobenzene ( 89 % ) as a red oil , b.p. 160-162 ° / 1 nm . , which solidified to a red solid , m.p. 38-39 ° ( lit. , m.p. 37-39 ° ) ( Found : C , 83.65 ; H , 5 · 4 ; N , 10 ...
Page 237
... obtained by extrapolation of the shift versus temperature curve to 0 ° K ) and use of the molarity concentration scale in the previous procedure 21 no longer gives the previously obtained value of n . Hence a new approach for finding n ...
... obtained by extrapolation of the shift versus temperature curve to 0 ° K ) and use of the molarity concentration scale in the previous procedure 21 no longer gives the previously obtained value of n . Hence a new approach for finding n ...
Page 238
... obtained for solutions of solute molecules at various concentrations in benzene only , plots of log ( 8 / [ SAB — 8 ] ... obtained for various molecules are shown in the Table , together with the values of SAB obtained by extrapolation of ...
... obtained for solutions of solute molecules at various concentrations in benzene only , plots of log ( 8 / [ SAB — 8 ] ... obtained for various molecules are shown in the Table , together with the values of SAB obtained by extrapolation of ...
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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Common terms and phrases
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
Bibliographic information
| Title | Quarterly Journal of the Chemical Society of London, Volume 1 |
| Author | Chemical Society (Great Britain) |
| Contributor | Royal Society of Chemistry (Great Britain) |
| Published | 1970 |
| Original from | the University of Michigan |
| Digitized | 20 Jul 2007 |
| Export Citation | BiBTeX EndNote RefMan |