Quarterly Journal of the Chemical Society of London, Volume 1 |
From inside the book
Results 1-3 of 68
Page 85
... possible . The calculated statistical abundances of C213CH , D2 + m / e 44 To throw light on the possible mechanisms by which the hydrogens and carbons of CH , + ( generated from n - C , H , + ) become equivalent before losing methane ...
... possible . The calculated statistical abundances of C213CH , D2 + m / e 44 To throw light on the possible mechanisms by which the hydrogens and carbons of CH , + ( generated from n - C , H , + ) become equivalent before losing methane ...
Page 212
... possible configurational isomers of trimethyl 1 - methylcyclohexane - 1,2,3 - tricarboxylate . Two of the isomers undergo highly stereoselective methylation at the 3 - position ; the third cannot be methylated under similar conditions ...
... possible configurational isomers of trimethyl 1 - methylcyclohexane - 1,2,3 - tricarboxylate . Two of the isomers undergo highly stereoselective methylation at the 3 - position ; the third cannot be methylated under similar conditions ...
Page 221
... possible structure of an intermediate of the cis - form occurring after the transition state , while TOR- represents the ion from the trans - form . If the attack of the base on C takes place in the rate - determining step , then the ...
... possible structure of an intermediate of the cis - form occurring after the transition state , while TOR- represents the ion from the trans - form . If the attack of the base on C takes place in the rate - determining step , then the ...
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 |
25 other sections not shown
Other editions - View all
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 |