Problem 139
Question
The approximate \(\mathrm{pH}\) of a solution formed by mixing equal volumes of solutions of \(0.1 \mathrm{M}\) sodium propionate and \(0.1 \mathrm{M}\) propanoic acid (the dissociation constant of propanoic acid is \(1.3 \times 10^{-5} \mathrm{~mol} \mathrm{dm}^{-3}\) ) will be (a) \(2.45\) (b) \(4.89\) (c) \(5.98\) (d) \(6.89\)
Step-by-Step Solution
Verified Answer
The approximate \(\mathrm{pH}\) of the solution is \(4.89\) (option b).
1Step 1: Identify the System
We have a solution containing equal volumes of sodium propionate and propanoic acid. This forms a buffer solution. The sodium propionate acts as the salt of the weak acid, propanoic acid.
2Step 2: Use the Henderson-Hasselbalch Equation
For a buffer solution, we can use the Henderson-Hasselbalch equation: \[ \mathrm{pH} = \mathrm{pK}_a + \log \frac{[\text{salt}]}{[\text{acid}]} \]In this case, both the concentrations of the salt (sodium propionate) and the acid (propanoic acid) are the same: \(0.1 \mathrm{M}\). Therefore, the ratio \(\log \frac{[\text{salt}]}{[\text{acid}]}\) is \(\log 1 = 0\).
3Step 3: Calculate pKa from Ka
The dissociation constant \(K_a\) of propanoic acid is given as \(1.3 \times 10^{-5}\). To find \(\mathrm{pK}_a\), use the formula: \[ \mathrm{pK}_a = -\log K_a \]Substituting the given \(K_a\) value:\[ \mathrm{pK}_a = -\log (1.3 \times 10^{-5}) = 4.89 \]
4Step 4: Apply to Henderson-Hasselbalch Equation
Since the concentrations of acid and salt are equal, the \(\mathrm{pH}\) is just the \(\mathrm{pK}_a\) calculated:\[ \mathrm{pH} = 4.89 + 0 = 4.89 \]
5Step 5: Conclusion
Comparing the calculated \(\mathrm{pH}\) with the provided options, the approximate \(\mathrm{pH}\) of the solution is option (b) \(4.89\).
Key Concepts
Henderson-Hasselbalch EquationpH CalculationDissociation ConstantAcid-Base Chemistry
Henderson-Hasselbalch Equation
Buffer solutions help maintain a stable pH when acids or bases are added to them. When dealing with buffer solutions, the Henderson-Hasselbalch equation is a crucial tool for understanding and predicting the pH of the solution. The Henderson-Hasselbalch equation is expressed as:
\[ \mathrm{pH} = \mathrm{pK}_a + \log \frac{[\text{salt}]}{[\text{acid}]} \]
This equation relates the pH of a buffer solution to the concentration of the acid and its conjugate base (often a salt). It is especially useful when the concentrations of these components are known, allowing for straightforward pH calculation. In the exercise, since the concentrations of sodium propionate (the salt) and propanoic acid (the acid) were equal, it simplified the use of this equation tremendously.
\[ \mathrm{pH} = \mathrm{pK}_a + \log \frac{[\text{salt}]}{[\text{acid}]} \]
This equation relates the pH of a buffer solution to the concentration of the acid and its conjugate base (often a salt). It is especially useful when the concentrations of these components are known, allowing for straightforward pH calculation. In the exercise, since the concentrations of sodium propionate (the salt) and propanoic acid (the acid) were equal, it simplified the use of this equation tremendously.
- Key Element: The ability to predict pH from known concentrations.
- Application: Especially useful in buffering solutions such as biological buffers.
pH Calculation
Calculating the pH of a solution is central to acid-base chemistry. pH is a measure of how acidic or basic a solution is, on a scale from 0 to 14.
A lower pH (0-6) indicates acidity, while a higher pH (8-14) indicates basicity, with 7 being neutral.
A lower pH (0-6) indicates acidity, while a higher pH (8-14) indicates basicity, with 7 being neutral.
- For strong acids and bases, pH can directly reflect the concentration of hydrogen or hydroxide ions in solution.
- For weak acids or buffers, as in our example, the calculation depends on both dissociation constant and concentrations.
Dissociation Constant
The dissociation constant, often denoted as \(K_a\) for acids, is an important parameter in acid-base chemistry. It quantifies the tendency of an acid to dissociate into its ions in solution.
For propanoic acid in the problem, the dissociation constant \(K_a\) was given as \(1.3 \times 10^{-5}\).
\[ \mathrm{pK}_a = - \log K_a \]
For instance, the \(\mathrm{pK}_a\) for propanoic acid was calculated to be 4.89, showing it's a weak acid. Understanding the dissociation constant helps predict the behavior of acids in different chemical contexts, including reactivity and equilibrium.
For propanoic acid in the problem, the dissociation constant \(K_a\) was given as \(1.3 \times 10^{-5}\).
- High \(K_a\) value: The acid dissociates more in water, indicating a stronger acid.
- Low \(K_a\) value: Less dissociation, indicating a weaker acid.
\[ \mathrm{pK}_a = - \log K_a \]
For instance, the \(\mathrm{pK}_a\) for propanoic acid was calculated to be 4.89, showing it's a weak acid. Understanding the dissociation constant helps predict the behavior of acids in different chemical contexts, including reactivity and equilibrium.
Acid-Base Chemistry
Acid-base chemistry involves the study of how acids and bases react with one another, a fundamental area in chemistry. Acids are substances that can donate a proton (H+), while bases can accept a proton or donate an electron pair in some reactions.
The mixing of sodium propionate and propanoic acid in the exercise creates a classic acid-base environment at equilibrium.
The mixing of sodium propionate and propanoic acid in the exercise creates a classic acid-base environment at equilibrium.
- Concept: Acids, such as propanoic acid, interact with bases, leading to ion formation and potential pH change.
- Buffer Systems: A buffer resists changes to pH upon addition of small amounts of acid or base as seen in the solution.
Other exercises in this chapter
Problem 136
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The \(\mathrm{pH}\) of \(0.05 \mathrm{M}\) aqueous solution of diethylamine is 12\. Its \(\mathrm{K}_{b}\) is (a) \(2 \times 10^{-3}\) (b) \(2.5 \times 10^{-3}\
View solution Problem 140
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View solution Problem 141
If the equilibrium constant of the reaction of weak acid HA with strong base is \(10^{9}\), then \(\mathrm{pH}\) of \(0.1 \mathrm{M} \mathrm{NaA}\) is (a) 3 (b)
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