Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 65
... determined thus differ in a consistent manner from those found for aqueous solutions . U.v. spectra were determined with a Unicam SP 800 spectrophotometer for 104 M - solutions at pH values such that the free base , monocation , or ...
... determined thus differ in a consistent manner from those found for aqueous solutions . U.v. spectra were determined with a Unicam SP 800 spectrophotometer for 104 M - solutions at pH values such that the free base , monocation , or ...
Page 66
... determined at pH 11-7 , but differs significantly from that determined for a solution in 0.01 N - acid . [ 8/1144 Received , August 7th , 1968 ] COMPOUNDS in which a phenyl ring is unequivocally attached to the imino- ( I and II ) or ...
... determined at pH 11-7 , but differs significantly from that determined for a solution in 0.01 N - acid . [ 8/1144 Received , August 7th , 1968 ] COMPOUNDS in which a phenyl ring is unequivocally attached to the imino- ( I and II ) or ...
Page 559
... determined by a single - crystal X - ray analysis . The crystals are orthorhombic , space group P2,2121 with four molecules of C17H2303Br in a unit cell of dimensions a = 7.70 , b = 9.70 , c = 22.93 Å . The structure was solved by the ...
... determined by a single - crystal X - ray analysis . The crystals are orthorhombic , space group P2,2121 with four molecules of C17H2303Br in a unit cell of dimensions a = 7.70 , b = 9.70 , c = 22.93 Å . The structure was solved by the ...
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