Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 17, Problem 17.25P

(a)

Interpretation Introduction

Interpretation:

Stronger acid in the given set of compounds has to be selected.

Concept introduction:

Acid - ionization constantKa:

Acids ionize in water.  Strong acids ionize completely whereas weak acids ionize to some limited extent.

The degree to which a weak acid ionizes depends on the concentration of the acid and the equilibrium constant for the ionization.

The ionization of a weak acid HA can be given as follows,

HA(aq)H+(aq)+A-(aq)

The equilibrium expression for the above reaction is given below.

Ka=[H+][A-][HA]

Where,

  Ka is acid ionization constant,

  [H+]  is concentration of hydrogen ion

  [A-]  is concentration of acid anion

           [HA] is concentration of the acid

pKa=logKapKb=logKb

Smaller value of pKa, stronger the acid, smaller the pKb, stronger the base.

(b)

Interpretation Introduction

Interpretation:

Stronger acid in the given set of compounds has to be selected.

Concept introduction:

Acid - ionization constantKa:

Acids ionize in water.  Strong acids ionize completely whereas weak acids ionize to some limited extent.

The degree to which a weak acid ionizes depends on the concentration of the acid and the equilibrium constant for the ionization.

The ionization of a weak acid HA can be given as follows,

HA(aq)H+(aq)+A-(aq)

The equilibrium expression for the above reaction is given below.

Ka=[H+][A-][HA]

Where,

  Ka is acid ionization constant,

  [H+]  is concentration of hydrogen ion

  [A-]  is concentration of acid anion

           [HA] is concentration of the acid

Smaller value of Ka, weaker the acid

Large value of Ka, stronger acid.

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Chapter 17 Solutions

Organic Chemistry

Ch. 17 - Write the IUPAC name of each compound, showing...Ch. 17 - Prob. 17.8PCh. 17 - Prob. 17.9PCh. 17 - Prob. 17.10PCh. 17 - Prob. 17.11PCh. 17 - Prob. 17.12PCh. 17 - Prob. 17.13PCh. 17 - On a cyclohexane ring, an axial carboxyl group has...Ch. 17 - Prob. 17.15PCh. 17 - Prob. 17.16PCh. 17 - Prob. 17.17PCh. 17 - Complete each reaction.Ch. 17 - Prob. 17.19PCh. 17 - Prob. 17.20PCh. 17 - Prob. 17.21PCh. 17 - Show the reagents and experimental conditions...Ch. 17 - Prob. 17.23PCh. 17 - Prob. 17.24PCh. 17 - Prob. 17.25PCh. 17 - In each set, assign the acid its appropriate pKa.Ch. 17 - Low-molecular-weight dicarboxylic acids normally...Ch. 17 - Complete the following acid-base reactions. (a)...Ch. 17 - Prob. 17.29PCh. 17 - Prob. 17.30PCh. 17 - Excess ascorbic acid is excreted in the urine, the...Ch. 17 - Give the expected organic product when...Ch. 17 - Show how to convert trans-3-phenyl-2-propenoic...Ch. 17 - Show how to convert 3-oxobutanoic acid...Ch. 17 - Prob. 17.35PCh. 17 - Prob. 17.36PCh. 17 - Prob. 17.37PCh. 17 - When 4-hydroxybutanoic acid is treated with an...Ch. 17 - Fischer esterification cannot be used to prepare...Ch. 17 - Draw the product formed on thermal decarboxylation...Ch. 17 - Prob. 17.41PCh. 17 - Show how cyclohexanecarboxylic acid could be...Ch. 17 - Prob. 17.43PCh. 17 - Prob. 17.44PCh. 17 - Prob. 17.45PCh. 17 - Write the products of the following sequences of...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Prob. 17.51PCh. 17 - Complete the following Fischer esterification...Ch. 17 - Prob. 17.53P
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General Chemistry | Acids & Bases; Author: Ninja Nerd;https://www.youtube.com/watch?v=AOr_5tbgfQ0;License: Standard YouTube License, CC-BY