Quarterly Journal of the Chemical Society of London, Part 2, Pages 1-1256 |
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Page 279
... molecules $ * 108 ° 00 ' - B1 — B2 -2.28 Ref . § Tcx t 2.13 0.03 108 ° 32 ' -0.78 236 1.43 0.02 108 ° 06 ' -3.47 236 3.26 0.03 105 ° 04 ' ............ 105 ° 40 ' Molecule HCC1s CH , CCI , HCBr , HCBг3 HCI , ............ Hence , we are ...
... molecules $ * 108 ° 00 ' - B1 — B2 -2.28 Ref . § Tcx t 2.13 0.03 108 ° 32 ' -0.78 236 1.43 0.02 108 ° 06 ' -3.47 236 3.26 0.03 105 ° 04 ' ............ 105 ° 40 ' Molecule HCC1s CH , CCI , HCBr , HCBг3 HCI , ............ Hence , we are ...
Page 361
... molecules on the adsorbent surface , but the acid molecules seem to be associated with some water molecules in the adsorbed phase . The acid molecules in the adsorbed phase are thus linked by hydrogen - bonding intermolecularly with ...
... molecules on the adsorbent surface , but the acid molecules seem to be associated with some water molecules in the adsorbed phase . The acid molecules in the adsorbed phase are thus linked by hydrogen - bonding intermolecularly with ...
Page 362
... molecules on adsorption , with the adsorbed phase containing some water molecules , the amount of water decreasing with increasing bulk concentration of acid . The nature of the aqueous solutions of the dicarboxylic acids is not fully ...
... molecules on adsorption , with the adsorbed phase containing some water molecules , the amount of water decreasing with increasing bulk concentration of acid . The nature of the aqueous solutions of the dicarboxylic acids is not fully ...
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absorption alkaline alkyl Amer amine anhydride anion aqueous aromatic atom b₁ benzene bond boron trifluoride bromide calculated carbon tetrachloride cation Chem chemical shifts Chemistry chloride coefficient compounds concentration conformation corresponding cyclohexane decomposition derived diazotisation dimethylformamide dioxan dipole effect electron equation equilibrium ester ether experimental Figure first-order formamide fraction H₂O hydration hydrogen hydrogen-bonding hydrolysis hydroxide initial iodide ionisation isomer k₂ kcal ketone kinetic Le Fèvre magnetic resonance measurements methanol methoxide methyl methylene mixture molar Kerr constants mole mole-¹ molecular molecules nitrogen nitrosation nitrous nucleophilic observed obtained oxide oxime oxygen perchloric acid phenyl phosphate Phys polarisability protons pyridine R. J. W. Le Fèvre radical rate constants ratio reaction reactivity recrystallised ring shown sodium sodium hydroxide solution solvation solvent species spectra spectrum structure substituent sulphone Table temperature ultraviolet values