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

Short Answer

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

Step by step solution

01

Defining strong and weak acids

A strong acid is an acid that completely dissociates in water, while a weak acid is an acid that dissociates partially in water. In other words, strong acids have a greater tendency to donate a proton (H+) to a solution than weak acids, making the resulting solution more acidic.
02

Understanding pKa and Ka values

The Ka value, also known as the acid dissociation constant, is a measure of the strength of an acid in a solution. The larger the Ka value, the stronger the acid. On the other hand, the pKa value is the negative logarithm of the Ka value (pKa = -log(Ka)). Therefore, the smaller the pKa value, the stronger the acid. (a)
03

Comparing pKa values for strong and weak acids

Since strong acids have larger Ka values, their corresponding pKa values would be smaller (due to the negative logarithm). Therefore, the pKa of a strong acid is smaller than the pKa of a weak acid. So, the weak acid has a larger numerical value for pKa. (b)
04

Comparing Ka values for strong and weak acids

By definition, a strong acid has a larger Ka value than a weak acid. So, the Ka of a strong acid is larger than the Ka of a weak acid. In conclusion: (a) The pKa of a weak acid has a larger numerical value. (b) The Ka of a strong acid has a larger numerical value.

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Most popular questions from this chapter

Answer true or false to the following statements about the mechanism of acid- base reactions. (a) The acid and base must encounter each other by a collision in order for the proton to transfer. (b) All collisions between acids and bases result in proton transfer. (c) During an acid-base reaction the lone pair on the base fills the A-H antibonding sigma orbital.

In each of the following three reaction coordinate diagrams, state: (a) Whether the reaction is exothermic or endothermic. (b) Whether the reaction is the slowest, the fastest, or intermediate in rate. (c) If all three reactions have the same entropy change between the reactant and product, which reaction has the largest favorable \(\Delta G^{0}\).

Glutamic acid is another of the amino acids found in proteins (Chapter 27). Glutamic acid has two carboxyl groups, one with \(\mathrm{p} K_{\mathrm{a}} 2.10\) and the other with \(\mathrm{p} K_{\mathrm{a}} 4.07\). (a) Which carboxyl group has which \(\mathrm{p} K_{\mathrm{a}}\) ? (b) Account for the fact that one carboxyl group is a considerably stronger acid than the other carboxyl group.

Write an equation for the reaction between each Lewis acid-base pair, showing electron flow by means of curved arrows. (a) \(\left(\mathrm{CH}_{3} \mathrm{CH}_{2}\right)_{3} \mathrm{~B}+\mathrm{OH}^{-} \longrightarrow\) (b) \(\mathrm{CH}_{3} \mathrm{Cl}+\mathrm{AlCl}_{3} \longrightarrow\)

Write an equation for the acid-base reaction between 2,4-pentanedione and sodium ethoxide and calculate its equilibrium constant, \(K_{\mathrm{eq}}\). The \(\mathrm{p} K_{\mathrm{a}}\) of 2,4 -pentanedione is 9 ; that of ethanol is \(15.9\).

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