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TÜBİTAK

Journal

2002

Potentiometry

Articles 1 - 2 of 2

Full-Text Articles in Physical Sciences and Mathematics

The Protonation Constants Of Some Aliphatic Alkylamines In Ethanol-Water Mixtures, Esma Kiliç, Gülteki̇n Gökçe, Esi̇n Canel Jan 2002

The Protonation Constants Of Some Aliphatic Alkylamines In Ethanol-Water Mixtures, Esma Kiliç, Gülteki̇n Gökçe, Esi̇n Canel

Turkish Journal of Chemistry

Protonation constants of methyl-, ethyl-, propyl- and butylamines Were determined potentiometrically using an electrode system calibrated in concentration units of hydrogen ion in ethanol-water mixtures (10\% -80\% ethanol, v/v) at an ionic strength of 0.1 and at 25°C. The trend in the values of protonation constants of these aliphatic amines was explained in terms of the number of alkyl groups and solvent composition. The basicity orders were found to be NH_{3} < R_{3}N < RNH_{2} < R_{2}NH (R:-CH_{3}, -C_{2}H_{5}, -n-C_{3}H_{7} and --n-C_{4}H_{9}) in all the solvent mixtures studied.


Acid-Base Equilibria Of Some N-Substituted Thiophene-2-Carboxamidoximes In Non-Aqueous Media, Nedi̇me Dürüst, Yaşar Dürüst, İlknur Meri̇ç Jan 2002

Acid-Base Equilibria Of Some N-Substituted Thiophene-2-Carboxamidoximes In Non-Aqueous Media, Nedi̇me Dürüst, Yaşar Dürüst, İlknur Meri̇ç

Turkish Journal of Chemistry

The protonation constants of the amino nitrogens of some N-substituted thiophene-2-carboxamidoximes have been determined in acetic acid by means of potentiometric titration with perchloric acid. pK_{a} values of the title compounds were interpreted on the basis of structural effects due to the substituents and the main skeleton.