Tautomerization of acetylacetone and relation of the tautomerization constant to other equilibrium parameters

1987 ◽  
Vol 52 (12) ◽  
pp. 2850-2858
Author(s):  
Jiří Mollin ◽  
Jitka Dopitová ◽  
Oldřiška Staňková

The relative partial pressures of acetylacetone above mixed aqueous-organic solutions were measured chromatographically and the Gibbs energies of acetylacetone transfer from water to the mixed solvents were determined and separated into contributions from the keto and enol forms. The tautomerization equilibrium was related to other thermodynamic equilibria and the Gibbs energy of transfer of the keto form was correlated with that of acetone.

Author(s):  
G. Bandyopadhyay ◽  
R. Mondal ◽  
Sujit Chandra Lahiri

AbstractThe dissociation constants of p-nitroaniline (B) (A critical assessment of the solvent-sorting equilibrium method using p-nitroaniline as indicator has been made. The method is not suitable to determine the Gibbs energy of transfer of H


Author(s):  
S. K. Gumtya ◽  
Sujit Chandra Lahiri ◽  
S. Aditya

The dissociation constants of the simplest dibasic organic acid, oxalic acid were determined conductometrically and pH metrically in ethanol + water mixtures (0–87 wt% of ethanol). These data were coupled with solubility values of oxalic acid and potassium hydrogen oxalate to calculate the Gibbs energies of transfer of oxalic acid, bioxalate(HOXThe p[H


1998 ◽  
Vol 63 (3) ◽  
pp. 293-298
Author(s):  
Vladislav Holba

The solubilities of cesium dianilinetetraisothiocyanatochromate(III) in water as well as in aqueous methanol, isopropyl alcohol, tert-butyl alcohol and acetonitrile were measured as a function of temperature and solvent composition. The Gibbs energies, enthalpies and entropies of transfer of the salt from water to the given solvents have been evaluated from experimental data. The contribution of [Cr(C6H5NH2)2(NCS)4]- ion to the Gibbs energy of transfer of the investigated salt has been calculated using the tetraphenylarsonium tetraphenylborate (TATB) reference electrolyte assumption.


2002 ◽  
Vol 216 (6) ◽  
Author(s):  
G. Bandyopadhyay ◽  
Sujit Chandra Lahiri

The thermodynamic dissociation constants for isoelectric reactions of the type LHAttempts were made to understand the basicity and structuredness of acetonitrile + water mixtures from a comparative study of Δ


1984 ◽  
Vol 39 (6) ◽  
pp. 600-602
Author(s):  
S. Janardhanan ◽  
C. Kalidas

The solubiltiy of silver bromate, the Gibbs transfer energy of Ag+ and BrO3- and the solvent transport number in methanol-dimethyl sulfoxide mixtures are reported. The solubility of silver bromate increases with addition of DMSO. The Gibbs energy of transfer of the silver ion (based on the ferrocene reference method) decreases, while that of the bromate ion becomes slightly negative with the addition of DMSO. The solvent transport number A passes through a maximum (⊿ = 1.0 at XDMSO = 0.65. From these results, it is concluded that the silver ion is preferentially solvated by DMSO whereas the bromate ion shows no preferential solvation.


1977 ◽  
Vol 31a ◽  
pp. 585-590 ◽  
Author(s):  
Antti Vesala ◽  
Juho-Pertti Jalava ◽  
Pentti Salomaa ◽  
H. Svanholt ◽  
Paul Hagenmuller ◽  
...  

Author(s):  
G. Bandyopadhyay ◽  
Sujit Chandra Lahiri

AbstractThe thermodyamic dissociation constants for isoelectric reaction of the type LHAttempts have been made to understand the basicity and structural properties of acetone + water mixtures from a comparative study of ΔG


2013 ◽  
Vol 26 (2) ◽  
pp. 351-358 ◽  
Author(s):  
Patrick Gan ◽  
Denise Lowinsohn ◽  
John S Foord ◽  
Richard G Compton

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