基于电导参数的2-取代4-甲酰基苯甲酸解离常数研究

Pub Date : 2023-02-08 DOI:10.5541/ijot.1136209
Kosrat N. Kaka, R. Omer, Salam G. Taher, W. M. H. Hamad
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引用次数: 0

摘要

解离常数是溶液中酸的强度的定量量度。本研究考察了邻烷氧基-4-甲酰苯甲酸等系列取代酸的解离常数。使用(2-甲氧基乙醇)作为溶剂有助于研究期望在293.15 ~ 318.15K不同温度下形成自由离子或溶剂分离离子对,并使用电导法进行了研究。研究的目的是利用fuss - hsia最小化技术计算解离常数、无限稀释时的等效电导和瓦尔登积(修正和完全)方程。结果发现,基于统计平方和的计算值(实际值与理论值不同)是无限稀释时的等效电导和解离常数。还观察到,温度的升高导致无限稀释时摩尔电导的增加和结合力的增加。此外,取代的烷氧基也影响化合物的解离。在本研究中,热力学参数(Ho,Go和So)也进行了评估和讨论。最后,根据取代基对解离常数的中介效应(M)和诱导效应(I)原理,研究并解释了取代基对解离速率的影响。
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Dissociation Constant Studies of 2-Substituted 4-Formylbenzoic Acid based on Conductometric Parameters using Fuoss-Hsia Theories
The dissociation constant is a quantitative measure of the strength of an acid in solution. This study examines dissociation constant for the series substituted acids like Ortho-alkoxy-4-formylbenzoic acid. The use of (2-methoxy ethanol) as a solvent contributed to the study expected to form free ions or solvent separated ion pair which has been studied with the use conductometric method at different temperatures ranged from 293.15 to 318.15K. The study aims at figuring out dissociation constant, equivalent conductance at infinity dilution, and Walden product by minimization technique using Fuoss-Hsia for both (Modified and Complete) equations. It has been found in the results that the calculated values based on statistical sum square (different between practical and theoretical values) is equivalent conductance at infinity dilution and dissociation constant. It has also been observed that increase the temperature leads to the increase of the molar conductance at infinity dilution, and the increase in association. Moreover, the substituted alkoxy group also affected dissociation of compounds. In this study, the thermodynamic parameters (Ho, Go and So) have also been evaluated and discussed. Finally, the effect of substituent groups on rate of dissociation was studied and explained with agreement to the principles of mesomeric(M) and Inductive effect(I) of substituent groups on dissociation constant.
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