Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 119
... Energy of 6 - Dimethylaminofulvenes.- 48 N. Jonathan , S. Gordon , and B. P. Dailey , J. Chem . Phys . , 1962 , 36 , 2443 . 49 C. Ganter and J. D. Roberts , J. Amer . Chem . Soc . , 1966 , 88 , 741 ; S. L. Mannatt and D. D. Elleman ...
... Energy of 6 - Dimethylaminofulvenes.- 48 N. Jonathan , S. Gordon , and B. P. Dailey , J. Chem . Phys . , 1962 , 36 , 2443 . 49 C. Ganter and J. D. Roberts , J. Amer . Chem . Soc . , 1966 , 88 , 741 ; S. L. Mannatt and D. D. Elleman ...
Page 150
... energy was decreased the relative contributions of the two states would change . ' Calculations for a single - state model 5 indicate that the relative abundances of our ' metastable peaks ' should be independent of electron beam energy ...
... energy was decreased the relative contributions of the two states would change . ' Calculations for a single - state model 5 indicate that the relative abundances of our ' metastable peaks ' should be independent of electron beam energy ...
Page 441
... energy distribution , the frac- tion of sub - decomposition energy ' M + ions can be calculated and compared with the observed fraction of ion current carried by M + . However , since experi- mentally determined energy distributions are ...
... energy distribution , the frac- tion of sub - decomposition energy ' M + ions can be calculated and compared with the observed fraction of ion current carried by M + . However , since experi- mentally determined energy distributions are ...
Contents
Physical organic chemistry | 1 |
Aromatic reactivity Part XXXVIII Protodesilylation of 12dihydrobenzocyclobutene indan and tetralin | 12 |
Aromatic reactivity Part XL Additional substituent effects in protodetrimethylsilylation | 21 |
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absorption acetic acid activation added addition alcohol Amer analysis angles appears aqueous atom base benzene bond bromide calculated carbon carbon tetrachloride Chem chemical chloride compared complex compounds concentration conformation constants containing corresponding coupling derived described determined DISCUSSION effect electron energy equation esters ethanol ether expected experimental experiments factor Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate initial intermediate involving kinetic less measured mechanism method methyl mixing mixture mole molecular molecule nitration observed obtained occurs organic oxidation oxygen peaks peroxide Phys plot position possible prepared present pressure proton radical rate constants ratio reaction reactivity reduced relative reported requires resonance respectively ring salts shifts showed shown similar sodium solution solvent spectra spectrum structure studied substituent suggested Table temperature values yield