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Which has the larger numerical value? (a) The \(\mathrm{p} K_{a}\) of a strong acid or the \(\mathrm{p} K_{\mathrm{a}}\) of a weak acid (b) The \(K_{a}\) of a strong acid or the \(K_{a}\) of a weak acid

Short Answer

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Question: Compare the numerical values of the pKa and Ka of strong acids and weak acids. Answer: The pKa of a strong acid has a smaller numerical value than the pKa of a weak acid, while the Ka of a strong acid has a larger numerical value than the Ka of a weak acid.

Step by step solution

01

Definition of Strong and Weak Acids

A strong acid is an acid that dissociates completely in water, releasing all of its hydrogen ions (H+) into the solution. A weak acid only partially dissociates in water, releasing only a fraction of its hydrogen ions (H+). Examples of strong acids are hydrochloric acid (HCl), nitric acid (HNO3), and sulfuric acid (H2SO4). Examples of weak acids are acetic acid (CH3COOH) and carbonic acid (H2CO3).
02

Definition of pKa and Ka

The pKa is a measure of the acidity of a substance and is related to the acid dissociation constant (Ka) by the equation: pKa = \(-\log _{10}(K_{a})\). The smaller the pKa, the stronger the acid; a larger Ka value indicates the stronger the acid, since it measures the tendency of an acid to dissociate into its ions in a solution.
03

pKa of Strong and Weak Acids

Since a strong acid dissociates completely in water, it has a higher Ka value (indicating a stronger tendency to release hydrogen ions), which means it has a smaller pKa value. Conversely, a weak acid has a lower Ka value (indicating a weaker tendency to release hydrogen ions), which means it has a larger pKa value. Therefore, the pKa of a strong acid has a smaller numerical value than the pKa of a weak acid. Answer (a): The pKa of a strong acid has a smaller numerical value than the pKa of a weak acid.
04

Ka of Strong and Weak Acids

Since a strong acid dissociates completely in water, it has a higher Ka value compared to a weak acid, which partially dissociates in water. Therefore, the Ka of a strong acid has a larger numerical value than the Ka of a weak acid. Answer (b): The Ka of a strong acid has a larger numerical value than the Ka of a weak acid.

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Most popular questions from this chapter

Following is a structural formula for the tert-butyl cation. (We discuss the formation, stability, and reactions of cations such as this one in Chapter 6.) C[C+](C)C tert-Butyl cation (a carbocation) (a) Predict all \(\mathrm{C}-\mathrm{C}-\mathrm{C}\) bond angles in this cation. (b) What is the hybridization of the carbon bearing the positive charge? (c) Write a balanced equation to show its reaction as a Lewis acid with water. (d) Write a balanced equation to show its reaction as a Brønsted-Lowry acid with water.

Offer an explanation for the following observations. (a) \(\mathrm{H}_{3} \mathrm{O}^{+}\)is a stronger acid than \(\mathrm{NH}_{4}^{+}\). (b) Nitric acid, \(\mathrm{HNO}_{3}\), is a stronger acid than nitrous acid, \(\mathrm{HNO}_{2}\). (c) Ethanol and water have approximately the same acidity. (d) Trifluoroacetic acid, \(\mathrm{CF}_{3} \mathrm{COOH}\), is a stronger acid than trichloroacetic acid, \(\mathrm{CCl}_{3} \mathrm{COOH}\).

Each molecule or ion can function as a base. Write a structural formula of the conjugate acid formed by reaction of each with \(\mathrm{HCl}\). (a) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{OH}\) (b) \(\mathrm{HCH}\) (c) \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{NH}\) (d) \(\mathrm{HCO}_{3}^{-}\)

2,4-Pentanedione is a considerably stronger acid than is acetone (Chapter 19). Write a structural formula for the conjugate base of each acid and account for the greater stability of the conjugate base from 2,4 -pentanedione. CCC(C)=O CC(=O)C=C(C)C Acetone 2,4-Pentanedione \(\mathrm{p} K_{\mathrm{a}} 20.2\) \(\mathrm{p} K_{\mathrm{a}} 9\)

Sodium hydride, \(\mathrm{NaH}\), is available commercially as a gray-white powder. It melts at \(800^{\circ} \mathrm{C}\) with decomposition. It reacts explosively with water and ignites spontaneously upon standing in moist air. (a) Write a Lewis structure for the hydride ion and for sodium hydride. Is your Lewis structure consistent with the fact that this compound is a high- melting solid? Explain. (b) When sodium hydride is added very slowly to water, it dissolves with the evolution of a gas. The resulting solution is basic to litmus. What is the gas evolved? Why has the solution become basic? (c) Write an equation for the reaction between sodium hydride and 1-butyne, \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{C} \equiv \mathrm{CH}\). Use curved arrows to show the flow of electrons in this reaction.

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