Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 222
... derived from ( III ) . There are 5 polysaccharide structures and thus ten disaccharide residues , each having the glycosidic oxygen equatorial to both sugar rings . For any disac- charide , a large group adjacent to this oxygen is , by ...
... derived from ( III ) . There are 5 polysaccharide structures and thus ten disaccharide residues , each having the glycosidic oxygen equatorial to both sugar rings . For any disac- charide , a large group adjacent to this oxygen is , by ...
Page 396
... derived radicals have been shown in other ways to be good one - electron reducing agents 19,20,26 ( with the two aldehydes , the reducing agents are evi- dently the radicals derived from the corresponding hydrates 26 ) . However , the ...
... derived radicals have been shown in other ways to be good one - electron reducing agents 19,20,26 ( with the two aldehydes , the reducing agents are evi- dently the radicals derived from the corresponding hydrates 26 ) . However , the ...
Page 428
... derived from 9 - substituted anthracenes , we have calculated the induced moments x required to give agreement between the molar Kerr constants of the 1- and 9 - substituted molecules . The resultant moments , ( calc . ) , derived from ...
... derived from 9 - substituted anthracenes , we have calculated the induced moments x required to give agreement between the molar Kerr constants of the 1- and 9 - substituted molecules . The resultant moments , ( calc . ) , derived from ...
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 |
Copyright | |
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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