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If \(0.1 \mathrm{M}\) of a weak monobasic acid is taken and its percentage degree of ionization is \(1.34 \%\), then calculate its ionization constant: (a) \(0.8 \times 10^{-5}\) (b) \(1.79 \times 10^{-5}\) (c) \(0.182 \times 19^{-5}\) (d) None of these

Short Answer

Expert verified
The ionization constant is approximately \(1.79 \times 10^{-5}\). Option (b) is correct.

Step by step solution

01

Understanding the Problem

We have a weak monobasic acid with a molarity of 0.1 M and a percentage degree of ionization of 1.34%. Our goal is to find the ionization constant, known as the acid dissociation constant \(K_a\).
02

Calculate the Ionized Concentration

To find the concentration of ionized acid, we convert the percentage degree of ionization to a decimal by dividing by 100. Thus, the ionized concentration is: \( 0.1 \times \frac{1.34}{100} = 0.00134 \text{ M} \).
03

Write the Expression for the Weak Acid

For a weak monobasic acid, \( HA \), dissociating into ions, the chemical equation is: \( HA \rightleftharpoons H^+ + A^- \).
04

Determine Concentration of Ions

At equilibrium, the concentration of \(H^+\) and \(A^-\) are both 0.00134 M since the acid ionizes to produce an equal amount of \(H^+\) and \(A^-\). The concentration of the un-ionized acid remaining is \(0.1 - 0.00134 = 0.09866 \text{ M}\).
05

Calculate the Ionization Constant

The ionization constant \(K_a\) is calculated using the formula: \(K_a = \frac{[H^+][A^-]}{[HA]}\). Substituting the concentrations: \( K_a = \frac{(0.00134)(0.00134)}{0.09866} \approx 1.82 \times 10^{-5} \).
06

Select the Answer Option

Compare the calculated \(K_a\) of \(1.82 \times 10^{-5}\) with the answer choices. The closest option is \(0.182 \times 10^{-5}\) (option c), but option b, \(1.79 \times 10^{-5}\), corresponds more directly to typical formats with minor approximation error. Option (b) is the correct choice.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Weak Monobasic Acid
A weak monobasic acid is an acid that donates only one proton or hydrogen ion per molecule to an aqueous solution. "Monobasic" refers to this single ionizable proton. Weak acids are characterized by their incomplete dissociation in water, meaning that only a small fraction of the acid molecules dissociate into ions. This partial dissociation is what defines their weakness compared to strong acids, which fully ionize in solution. Understanding that a weak monobasic acid does not fully dissociate helps us in calculating the equilibrium position of the acid in solution and its corresponding acid dissociation constant.
Degree of Ionization
The degree of ionization refers to the fraction of the total amount of a weak acid that dissociates into ions in solution. It is usually expressed as a percentage. For example, if the degree of ionization of an acid is 1.34%, it means that 1.34% of the original acid molecules have donated their protons to the solution. To convert this percentage into a decimal to find how much of the acid actually ionizes, we divide it by 100. In our exercise, since the molarity of the acid is 0.1 M and its degree of ionization is 1.34%, the concentration of ionized acid is found by:
  • 0.1 M * (1.34/100) = 0.00134 M
This calculation is crucial in further determining the equilibrium concentrations in the solution.
Equilibrium Concentrations
When dealing with the equilibrium concentrations of ions in a weak acid solution, it’s important to understand that the acid does not completely dissociate. The acid equilibrium is reached when the rates of the forward and reverse reactions are equal. In the example with our weak monobasic acid, the chemical equation is represented as:
  • HA ↔ H⁺ + A⁻
At equilibrium, the concentration of hydrogen ions, \([H^+]\),and anions, \([A^-]\), is equal to the degree of ionization calculated. Thus, \([H^+]=[A^-] = 0.00134 \text{ M}\).The concentration of the undissociated acid, \([HA]\), is reduced by this same amount, since the acid has dissociated to give these ions. It is found using:
  • \([HA] = 0.1 \text{ M} - 0.00134 \text{ M} = 0.09866 \text{ M}\)
These concentrations are necessary to calculate the acid's ionization constant.
Acid Dissociation
Acid dissociation refers to the process by which an acid breaks down into ions in solution. For weak acids, this dissociation process reaches an equilibrium, which is described by the acid dissociation constant, denoted as \(K_a\). The formula to calculate this constant for a weak acid dissociating as \(HA \rightarrow H^+ + A^-\) is:\[K_a = \frac{[H^+][A^-]}{[HA]}\]Using the equilibrium concentrations determined earlier, the \(K_a\) can be calculated by:\[K_a = \frac{(0.00134)(0.00134)}{0.09866} = 1.82 \times 10^{-5}\] This value tells us the strength of the acid; a larger \(K_a\) implies a stronger acid due to the greater extent of ionization. In exercises like these, students often compare this calculated \(K_a\) with provided options to choose the closest answer. Here, the correct choice is option (b) \(1.79 \times 10^{-5}\), which reflects a small approximation error.

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Most popular questions from this chapter

At \(700 \mathrm{~K}\), the equilibrium constant \(\mathrm{K}_{\mathrm{p}}\) for the reaction \(2 \mathrm{SO}_{3}(\mathrm{~g}) \rightleftharpoons 2 \mathrm{SO}_{2}(\mathrm{~g})+\mathrm{O}_{2}(\mathrm{~g})\) is \(1.80 \times 10^{-3}\) What is the numerical value in mole per litre of equilibrium constant \(\mathrm{K}_{\mathrm{c}}\) for this reaction at the same temperature: (a) \(8.1 \times 10^{-8}\) (b) \(9.1 \times 10^{-9} \mathrm{~mol} \mathrm{~L}^{-1}\) (c) \(3.1 \times 10^{-7}\) (d) \(6.1 \times 10^{-7} \mathrm{~mol} \mathrm{~L}^{-1}\)

For a reversible reaction, the concentration of the reactants are doubled, then the equilibrium constant: (a) Becomes one-fourth (b) Is doubled (c) Is halved (d) Remains same

At \(\mathrm{Kp}\) for the following reaction is 1 atm \(\mathrm{X}(\mathrm{g}) \rightleftharpoons \mathrm{Y}(\mathrm{g})+\mathrm{Z}(\mathrm{g})\) At equilibrium, \(50 \%\) of \(\mathrm{X}(\mathrm{g})\) is dissociated. The total pressure of the equilibrium system is ' \(\mathrm{P}\) ' atm. what is the partial pressure (in atm) of \(X(g)\) at equilibrium: (a) 1 (b) 4 (c) 2 (d) \(0.5\)

For the hypothetical reactions, the equilibrium constant \((\mathrm{K})\) values are given: \(\mathrm{A} \rightleftharpoons \mathrm{B} \mathrm{K}_{1}=2\) \(\mathrm{B} \rightleftharpoons \mathrm{C} \mathrm{K}_{2}^{1}=4\) \(\mathrm{C} \rightleftharpoons \mathrm{D} \mathrm{K}_{3}^{2}=3\) The equilibrium constant \((\mathrm{K})\) for the reaction: \(\mathrm{A} \rightleftharpoons \mathrm{D}\) is (a) 3 (b) 6 (c) 12 (d) 24

The relation between \(K_{n}\) and \(K_{c}\) for the reaction \(2 \mathrm{NO}(\mathrm{g})+\mathrm{Cl}_{2}(\mathrm{~g}) \rightleftharpoons 2 \mathrm{NOCl}(\mathrm{g})\) is: (a) \(\mathrm{K}_{\mathrm{p}}=\mathrm{K}_{\mathrm{c}}(\mathrm{RT})^{-1}\) (b) \(\mathrm{K}_{\mathrm{p}}=\mathrm{K}_{\mathrm{c}}\) (c) \(K_{p}^{p}=K_{c} /(R T)^{2}\) (d) \(\mathrm{K}_{\mathrm{p}}=\mathrm{K}_{\mathrm{c}} / \mathrm{RT}\)

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