Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 74
Page 1316
... hydrogen bonds of this kind may be formed between the phenol and the methyl decanoate or oleyl alcohol , and these interactions should assist the transfer of the phenol from the aqueous phase to the organic phase . For the o ...
... hydrogen bonds of this kind may be formed between the phenol and the methyl decanoate or oleyl alcohol , and these interactions should assist the transfer of the phenol from the aqueous phase to the organic phase . For the o ...
Page 1411
... hydrogen phosphate ( IV ; R = Me , R ′ == H ) , and 1 - methyluridine - 5 ′ methyl hydrogen phosphate were 0.17 , 0.26 , and 0.52 , respectively . The trace of material with RF 0-62 in the last experiment was assumed to be 1 ...
... hydrogen phosphate ( IV ; R = Me , R ′ == H ) , and 1 - methyluridine - 5 ′ methyl hydrogen phosphate were 0.17 , 0.26 , and 0.52 , respectively . The trace of material with RF 0-62 in the last experiment was assumed to be 1 ...
Page 1642
... hydrogen - bonded OH ( 3500 cm . - 1 ) , non - hydrogen- bonded -NH , ( 3328 +3250 cm . - 1 , as in trans- [ Co en , Cl2 ] Cl ) , unusually strong unsym- metrical hydrogen bonds ( broad bands at 2480 and 1940 cm . - 1 ) , and ...
... hydrogen - bonded OH ( 3500 cm . - 1 ) , non - hydrogen- bonded -NH , ( 3328 +3250 cm . - 1 , as in trans- [ Co en , Cl2 ] Cl ) , unusually strong unsym- metrical hydrogen bonds ( broad bands at 2480 and 1940 cm . - 1 ) , and ...
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Common terms and phrases
1-methylheptyl 1-phenylethyl bromide absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine anhydride aniline aqueous atom benzene bond Calc calculated carbon Chem chloride chloroform CHPh chromatography cm.¹ complex compounds concentration crystallised cyanohydrin derivative diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated EXPERIMENTAL extracted formation formed Found fraction gave H₂O halides hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum isomers k₁ k₂ kcal ketone kinetic ligand magnesium manganese(III methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical oxaloacetic acid oxidation peaks peroxide petroleum b. p. phenols phosphate phosphine picryl potassium prepared proton pyridine rate coefficients reaction reflux requires residue room temperature rotation shown silanes sodium solution solvent spectra structure substituted sulphide sulphuric Table tetracyanoethylene titration tricyanovinyl values yield