Answered: Most of the pKa values given in this…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Most of the pKa values given in this text were determined in water. How would the pKa values of carboxylic acids, alcohols, ammonium ions (RNH32) , phenol, and an anilinium ion (C6H5NH32) change if they were determined in a solvent less polar than water?

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

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The strength of a chemical substance acidity is determined by its pKa value. It is actually the negative logarithm of acid dissociation constant value. Any substance dissociation is based on the type of solvent used. The general phenomenon is like dissolves like that is polar substances gets dissociated well in polar solvent and the non polar substance gets dissociated in non polar solvent.

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