Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1241
... ( mole - 1 ml . sec . - 1 ) = 12 · 3 ( 12,000 / 2.3RT ) . The Arrhenius parameters are in good agreement with results of other hydrogen abstractions by methyl radicals from alkanes , obtained by the same method . The activation energy ...
... ( mole - 1 ml . sec . - 1 ) = 12 · 3 ( 12,000 / 2.3RT ) . The Arrhenius parameters are in good agreement with results of other hydrogen abstractions by methyl radicals from alkanes , obtained by the same method . The activation energy ...
Page 1297
... mole ) was added dropwise during 15 min . to a stirred , boiling , methanolic ( 100 c.c. ) solution of the azo - compound ( 0.01 mole ) . The mixture was boiled under reflux for 1 hr . during which time the product separated ; it was ...
... mole ) was added dropwise during 15 min . to a stirred , boiling , methanolic ( 100 c.c. ) solution of the azo - compound ( 0.01 mole ) . The mixture was boiled under reflux for 1 hr . during which time the product separated ; it was ...
Page 1365
... mole of ( BH + ) aq from ( B ) aq respectively , while AH prot BH is the corresponding change BH is the corresponding change for the formation of one mole of ( BHO ) aq starting from ( BH † ) aq ; ¤ ̧н ̧0 + and ¤ ̧н + finally indicate ...
... mole of ( BH + ) aq from ( B ) aq respectively , while AH prot BH is the corresponding change BH is the corresponding change for the formation of one mole of ( BHO ) aq starting from ( BH † ) aq ; ¤ ̧н ̧0 + and ¤ ̧н + finally indicate ...
Contents
Dolcetti G See Peloso A 1506 | 1031 |
Structures of cyclic amides Part III Thio and selenolactams | 1033 |
Equilibria in solutions which contain a metal ion and an aminoacid | 1039 |
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¹H n.m.r. spectrum absorption acetaldehyde acetone acid adduct Amer anion aqueous atoms bands benzene bond bromine trifluoride calculated carbon catalyst cation Chem chemical Chemistry chloride cm.¹ co-ordination cobalt(II coefficients complexes compounds concentration configuration corresponding coupling constant crystals cyanide dehy gel dichloromethane dilute doublet electronic energy equation ethanol ether experimental Figure five-co-ordinate fluorine formation frequencies halide heat hydrogen hydrogen cyanide hydrolysis i.r. spectra Inorg iodide iodobenzene isomers k₁ kcal lactams ligand magnetic Mc./sec measured metal methyl mixture mmoles mole-¹ molecular molecule n.m.r. spectra nickel nickel(II nitric oxide nitrogen observed obtained octahedral orbital oxygen parameters phosphine phosphorus Phys plexes PMe,Ph potassium prepared present proton Raman reaction resonance room temperature sample scandium(III showed shown similar sodium solid solution solvent species structure sulphur Table thallium thio thiocyanate thiocyanogen thiolactams titration trans trimethylsilyl tris(trimethylsilyl values yellow