Calculate the \(\mathrm{pH}\) at the halfway point and at the equivalence point for each of the following titrations. a. \(100.0 \mathrm{mL}\) of \(0.10 \mathrm{M} \mathrm{HC}_{7} \mathrm{H}_{5} \mathrm{O}_{2}\left(K_{\mathrm{a}}=6.4 \times 10^{-5}\right)\) titrated by 0.10 \(M \mathrm{NaOH}\) b. \(100.0 \mathrm{mL}\) of \(0.10 \mathrm{M} \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{NH}_{2}\left(K_{\mathrm{b}}=5.6 \times 10^{-4}\right)\) titrated by 0.20 \(M \mathrm{HNO}_{3}\) c. \(100.0 \mathrm{mL}\) of \(0.50 \mathrm{M}\) HCl titrated by \(0.25 \mathrm{M} \mathrm{NaOH}\)

Short Answer

Expert verified
a. Halfway point: \(pH \approx 3.79\) Equivalence point: \(pH \approx 7.87\) b. Halfway point: \(pH \approx 10.61\) Equivalence point: \(pH \approx 7.66\) c. Halfway point: \(pH \approx 7.0\) Equivalence point: \(pH \approx 7.0\)

Step by step solution

01

Titration a: Halfway Point#Region_content#To find the pH at the halfway point for titration a, we need to use the Henderson-Hasselbalch equation given below, which states: \(pH = pK_a + \log \frac{[\mathrm{A}^-]}{[\mathrm{HA}]}\) Since we know the concentration of the weak acid (\(0.10 M\)), HC7H5O2, and that it is equal to the concentration of its conjugate base at the halfway point, we can plug these values into the Henderson-Hasselbalch equation, as well as the given \( K_a \) value. \( \)

Titration a: Halfway Point Calculations#Region_content#First, let's calculate \(pK_a\): \( pK_a = -\log{K_a} = -\log(6.4 \times 10^{-5}) \) Next, we will plug the values into Henderson-Hasselbalch equation: \( pH = (-\log(6.4 \times 10^{-5})) + \log \frac{[0.10]}{[0.10]} \) \( \)
02

Titration a: Equivalence Point#Region_content#At the equivalence point, the moles of acid (\(\mathrm{HC}_{7} \mathrm{H}_{5} \mathrm{O}_{2}\)) are equal to the moles of base (\(\mathrm{NaOH}\)). We first calculate the moles of acid and base before solving for the equilibrium concentrations and pH at the equivalence point. \( \)

Titration a: Equivalence Point Calculations#Region_content#Calculate the moles of \(\mathrm{HC}_{7} \mathrm{H}_{5} \mathrm{O}_{2}\) and \(\mathrm{NaOH}\): Moles of acid: \((0.1 \textrm{ M})(0.1 \textrm{ L}) = 0.01 \textrm{ mol}\) Amount of \(\mathrm{NaOH}\) required to reach the equivalence point (equal to moles of acid): \(0.01 \textrm{ mol}\) Volume of \(\mathrm{NaOH}\) required to reach the equivalence point: \(\frac{0.01 \textrm{ mol}}{0.1 \textrm{ M}} = 0.1 \textrm{ L}\) Total volume at equivalence point: \(0.1 \textrm{ L} + 0.1 \textrm{ L} = 0.2 \textrm{ L}\) Now we find the pH at the equivalence point using the ion-product of water: \(K_w = [\mathrm{H}^+][\mathrm{OH}^-] \) And the \(K_a\) of the conjugate base (\(\mathrm{C}_{7} \mathrm{H}_{5} \mathrm{O}_{2}^-\)): \(K_a = [\mathrm{HC}_{7} \mathrm{H}_{5} \mathrm{O}_{2}][\mathrm{OH}^{-}]/[\mathrm{C}_{7} \mathrm{H}_{5} \mathrm{O}_{2}^{-}]\) \( \)
03

Titration b: Halfway Point#Region_content#To find the pH at the halfway point for titration b, we need to use the equation for pOH: \(pOH = pK_b + \log \frac{[\mathrm{BH}^+]}{[\mathrm{B}]}\) Then convert the pOH value to pH value using: \(pH = 14 - pOH\) \( \)

Titration b: Halfway Point Calculations#Region_content#First, let's calculate \(pK_b\): \( pK_b = -\log{K_b} = -\log(5.6 \times 10^{-4}) \) Next, we will plug the values into pOH equation: \( pOH = (-\log(5.6 \times 10^{-4})) + \log \frac{[0.10]}{[0.10]} \) Finally, convert pOH to pH: \( pH = 14 - pOH \) \( \)
04

Titration b: Equivalence Point#Region_content#At the equivalence point, the moles of base (\(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{NH}_{2}\)) are equal to the moles of acid (\(\mathrm{HNO}_{3}\)). We first calculate the moles of base and acid before solving for the equilibrium concentrations and pH at the equivalence point. \( \)

Titration b: Equivalence Point Calculations#Region_content#First, calculate the moles of \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{NH}_{2}\) and \(\mathrm{HNO}_{3}\): Moles of base: \((0.1 \textrm{ M})(0.1 \textrm{ L}) = 0.01 \textrm{ mol}\) Amount of \(\mathrm{HNO}_{3}\) required to reach the equivalence point (equal to moles of base): \(0.01 \textrm{ mol}\) Volume of \(\mathrm{HNO}_{3}\) required to reach the equivalence point: \(\frac{0.01 \textrm{ mol}}{0.2 \textrm{ M}} = 0.05 \textrm{ L}\) Total volume at equivalence point: \(0.1 \textrm{ L} + 0.05 \textrm{ L} = 0.15 \textrm{ L}\) Now we find the pH at the equivalence point using the following equation: \(pH = 14 - pOH\) Where pOH can be calculated using the ion-product of water: \(K_w = [\mathrm{H}^+][\mathrm{OH}^-] \) \( \)
05

Titration c: Halfway Point#Region_content#In the titration of a strong acid (\(\textrm{HCl}\)) with a strong base (\(\textrm{NaOH}\)), pH at the halfway point can be directly determined by the average of their pKa values. \( \)

Titration c: Halfway Point Calculations#Region_content#Determine the average pKa value of HCl and NaOH: pH = \( \frac{pK_{a, \textrm{HCl}} + pK_{a, \textrm{NaOH}}}{2}\) Since \(\textrm{HCl}\) and \(\textrm{NaOH}\) are strong acids and bases, their pKa values are negligible, and the pH at the halfway point is about 7.0. \( \)
06

Titration c: Equivalence Point#Region_content#To find the pH at the equivalence point for a strong acid-strong base titration, we can directly determine the concentration of \([\mathrm{H}^+]\) ions in the solution. \( \)

Titration c: Equivalence Point Calculations#Region_content#First, calculate the moles of \(\textrm{HCl}\) and \(\textrm{NaOH}\): Moles of acid: \((0.5 \textrm{ M})(0.1 \textrm{ L}) = 0.05 \textrm{ mol}\) Amount of \(\textrm{NaOH}\) required to reach the equivalence point (equal to moles of acid): \(0.05 \textrm{ mol}\) Volume of \(\textrm{NaOH}\) required to reach the equivalence point: \(\frac{0.05 \textrm{ mol}}{0.25 \textrm{ M}} = 0.2 \textrm{ L}\) Total volume at equivalence point: \(0.1 \textrm{ L} + 0.2 \textrm{ L} = 0.3 \textrm{ L}\) Now we find the concentration of \([\mathrm{H}^+]\) and \([\mathrm{OH}^-]\) ions in the solution: \([\mathrm{H}^+] = \frac{\text{moles of } \mathrm{H}^+}{\textrm{total volume}} = \frac{0.05 \textrm{ mol}}{0.3 \textrm{ L}}\) \([\mathrm{OH}^-] = \frac{\text{moles of } \mathrm{OH}^-}{\textrm{total volume}} = \frac{0.05 \textrm{ mol}}{0.3 \textrm{ L}}\) Finally, calculate pH using the following equation: \(pH = -\log [\mathrm{H}^+]\)

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Most popular questions from this chapter

A student intends to titrate a solution of a weak monoprotic acid with a sodium hydroxide solution but reverses the two solutions and places the weak acid solution in the buret. After \(23.75 \mathrm{mL}\) of the weak acid solution has been added to \(50.0 \mathrm{mL}\) of the \(0.100 \mathrm{M} \mathrm{NaOH}\) solution, the \(\mathrm{pH}\) of the resulting solution is \(10.50 .\) Calculate the original concentration of the solution of weak acid.

When a person exercises, muscle contractions produce lactic acid. Moderate increases in lactic acid can be handled by the blood buffers without decreasing the pH of blood. However, excessive amounts of lactic acid can overload the blood buffer system, resulting in a lowering of the blood pH. A condition called acidosis is diagnosed if the blood pH falls to 7.35 or lower. Assume the primary blood buffer system is the carbonate buffer system described in Exercise \(45 .\) Calculate what happens to the \(\left[\mathrm{H}_{2} \mathrm{CO}_{3}\right] /\left[\mathrm{HCO}_{3}^{-}\right]\) ratio in blood when the \(\mathrm{pH}\) decreases from 7.40 to 7.35.

Calculate the \(\mathrm{pH}\) of each of the following buffered solutions. a. \(0.10 M\) acetic acid/0.25 \(M\) sodium acetate b. \(0.25 M\) acetic acid/0.10 \(M\) sodium acetate c. \(0.080 M\) acetic acid/0.20 \(M\) sodium acetate d. \(0.20 M\) acetic acid/0.080 \(M\) sodium acetate

What concentration of \(\mathrm{NH}_{4} \mathrm{Cl}\) is necessary to buffer a \(0.52-M\) \(\mathrm{NH}_{3}\) solution at \(\mathrm{pH}=9.00 ?\left(K_{\mathrm{b}} \text { for } \mathrm{NH}_{3}=1.8 \times 10^{-5} .\right)\)

The common ion effect for weak acids is to significantly decrease the dissociation of the acid in water. Explain the common ion effect.

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