Problem 3
Question
The pH of a 0.10 M HOBr solution is 4.8. a. What is \(\left[\mathrm{H}^{+}\right]\) in that solution? b. What is \(\left[\mathrm{OBr}^{-}\right] ?\) What is [HOBr]? (Where do the \(\mathrm{H}^{+}\) and \(\mathrm{OBr}^{-}\) ions come from?) c. What is the value of \(K_{\mathrm{a}}\) for HOBr? What is the value of \(\mathrm{pK}_{\mathrm{a}} ?\)
Step-by-Step Solution
Verified Answer
[H⁺]=1.58×10^{-5} M, [OBr⁻]=1.58×10^{-5} M, [HOBr]≈0.10 M, Kₐ≈2.50×10^{-9}, pKₐ≈8.60.
1Step 1: Calculate [H⁺]
Given the pH of the solution is 4.8, we use the formula to find the concentration of hydrogen ions \([\mathrm{H}^+]\): \([\mathrm{H}^+]=10^{-\text{pH}}\). Substituting the values, we get \([\mathrm{H}^+]=10^{-4.8}\). Calculating this gives \([\mathrm{H}^+]=1.58\times10^{-5}\) M.
2Step 2: Identify Equilibrium Concentrations
In the dissociation of HOBr, \(\text{HOBr} \rightleftharpoons \text{H}^+ + \text{OBr}^-\). Initially, \([\text{HOBr}] = 0.10\) M. At equilibrium, \([\text{HOBr}]=0.10 - x\), \([\text{H}^+]=x\), \([\text{OBr}^-]=x\). Since \([\text{H}^+]=1.58\times10^{-5}\) M (from Step 1), \(x = 1.58\times10^{-5}\), thus \([\text{OBr}^-]=1.58\times10^{-5}\) M and \([\text{HOBr}]=0.10-1.58\times10^{-5}\approx0.10\) M.
3Step 3: Calculate Kₐ for HOBr
The expression for the acid dissociation constant \(K_a\) is: \(K_a = \frac{[\text{H}^+][\text{OBr}^-]}{[\text{HOBr}]}\). Substituting the equilibrium concentrations: \(K_a = \frac{(1.58\times10^{-5})(1.58\times10^{-5})}{0.10}\approx2.50\times10^{-9}\).
4Step 4: Calculate pKₐ for HOBr
To find \(\text{pK}_a\), use the relation \(\text{pK}_a = -\log(K_a)\). Substituting the value of \(K_a\): \(\text{pK}_a = -\log(2.50\times10^{-9})\approx8.60\).
Key Concepts
pH CalculationEquilibrium ConcentrationAcid Dissociation Constant (Ka)pKa Calculation
pH Calculation
Understanding pH Calculation is fundamental in acid-base chemistry. It represents the acidity or alkalinity of a solution. pH is calculated using the formula:
In our example with 0.10 M HOBr, the given pH is 4.8.
Using the formula \([ ext{H}^+] = 10^{-\text{pH}}\), we substitute the known pH value:
\([ ext{H}^+] = 10^{-4.8}\).
Calculating this gives:
- \[pH = -\log_{10} [\text{H}^+]\]
In our example with 0.10 M HOBr, the given pH is 4.8.
Using the formula \([ ext{H}^+] = 10^{-\text{pH}}\), we substitute the known pH value:
\([ ext{H}^+] = 10^{-4.8}\).
Calculating this gives:
- \[[ ext{H}^+] = 1.58\times10^{-5}\] M.
Equilibrium Concentration
Determining Equilibrium Concentrations is crucial for understanding the ratios of reactants and products in a chemical equilibrium. For the dissociation of HOBr in our example:
At equilibrium, we use the principle that the change in concentration for \(\text{H}^+\) and \(\text{OBr}^-\) is equal.
With our previously found hydrogen ion concentration \(1.58 \times 10^{-5}\) M,
The almost unchanged concentration of HOBr at equilibrium is a sign of a weak acid.
- \[\text{HOBr} \rightleftharpoons \text{H}^+ + \text{OBr}^-\]
At equilibrium, we use the principle that the change in concentration for \(\text{H}^+\) and \(\text{OBr}^-\) is equal.
With our previously found hydrogen ion concentration \(1.58 \times 10^{-5}\) M,
- \([ ext{OBr}^-] = [\text{H}^+] = 1.58 \times 10^{-5}\) M
The almost unchanged concentration of HOBr at equilibrium is a sign of a weak acid.
Acid Dissociation Constant (Ka)
The Acid Dissociation Constant, \(K_a\), is a measure of the strength of an acid in solution.
It quantifies the equilibrium concentrations between the acid and its ions.
For HOBr, the equilibrium expression is:
It quantifies the equilibrium concentrations between the acid and its ions.
For HOBr, the equilibrium expression is:
- \[K_a = \frac{[\text{H}^+][\text{OBr}^-]}{[\text{HOBr}]}\]
- \[[\text{H}^+] = 1.58\times10^{-5}\] M
- \[[\text{OBr}^-] = 1.58\times10^{-5}\] M
- \[[\text{HOBr}] \approx 0.10 M\]
- \[K_a \approx \frac{(1.58\times10^{-5})(1.58\times10^{-5})}{0.10}\approx2.50\times10^{-9}\]
pKa Calculation
Calculating pKa provides insight into the acid's strength.
It is derived from the acid dissociation constant, \(K_a\).
The formula relating \(K_a\) and pKa is:
Understanding the relationship between \(K_a\) and pKa helps chemists and students predict how an acid behaves in different environments.
It is derived from the acid dissociation constant, \(K_a\).
The formula relating \(K_a\) and pKa is:
- \[pK_a = -\log_{10}(K_a)\]
- \[pK_a = -\log_{10}(2.50\times10^{-9})\approx8.60\]
Understanding the relationship between \(K_a\) and pKa helps chemists and students predict how an acid behaves in different environments.
Other exercises in this chapter
Problem 2
An aqueous solution of \(\mathrm{NH}_{3}\) has a pH of \(11.6 .\) The ammonia (NH, \(_{3}\) ) molecule is the conjugate base of the NH_t (called "ammonium") ion
View solution Problem 4
Formic acid, HFor, has a \(K_{a}\) value equal to about \(1.8 \times 10^{-4} .\) A student is asked to prepare a buffer having a pH of 3.90 from a solution of f
View solution