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Data collected during the titration of a 20.0 mL sample of a 0.10 M solution of a monoprotic acid wiAcids and Bases Chemistry Question

Question

Data collected during the titration of a 20.0 mL sample of a 0.10 M solution of a monoprotic acid with a solution of NaOH of unknown concentration are plotted in the graph above. [VISUAL] Based on the data, which of the following are the approximate pKa of the acid and the molar concentration of the NaOH?

A.

pKa = 4.7; [NaOH] = 0.050 M

B.

pKa = 4.7; [NaOH] = 0.10 M

✓ Correct
C.

pKa = 9.3; [NaOH] = 0.050 M

D.

pKa = 9.3; [NaOH] = 0.10 M

💡 Solution & Explanation

STEPS:

1. Identify the equivalence point of the titration: The equivalence point on a titration curve of a weak acid with a strong base is represented by the point of maximum slope (the center of the near-vertical region of the pH curve). On the provided graph, this sharp vertical inflection occurs at exactly 20.0 mL of added NaOH.
2. Calculate the concentration of the NaOH titrant: At the equivalence point of a titration involving a monoprotic acid, the moles of added base (NaOH\text{NaOH}) must be stoichiometrically equal to the initial moles of the acid in the sample:
Moles of acid=Moles of NaOH\text{Moles of acid} = \text{Moles of NaOH}
Using the molarity and volume relationship (MAVA=MBVBM_A V_A = M_B V_B):
(0.10 M)×(20.0 mL)=MNaOH×(20.0 mL)(0.10\text{ M}) \times (20.0\text{ mL}) = M_{\text{NaOH}} \times (20.0\text{ mL})
Solving for the molarity of NaOH:
MNaOH=0.10 M×20.0 mL20.0 mL=0.10 MM_{\text{NaOH}} = \frac{0.10\text{ M} \times 20.0\text{ mL}}{20.0\text{ mL}} = \mathbf{0.10\text{ M}}
This narrows down the correct choice to either Option B or Option D.
3. Identify the half-equivalence point: The half-equivalence point occurs when exactly half of the volume of strong base required to reach the equivalence point has been added:
Vhalf-equivalence=Vequivalence2=20.0 mL2=10.0 mLV_{\text{half-equivalence}} = \frac{V_{\text{equivalence}}}{2} = \frac{20.0\text{ mL}}{2} = \mathbf{10.0\text{ mL}}
4. Relate the half-equivalence point pH to the pKap\text{K}_a: At this halfway point, exactly half of the weak acid (HA\text{HA}) molecules have reacted with the added OH\text{OH}^- to form the conjugate base (A\text{A}^-), resulting in equal concentrations of the weak acid and its conjugate base remaining in solution ([HA]=[A][\text{HA}] = [\text{A}^-]). Substituting this equality into the Henderson-Hasselbalch equation:
pH=pKa+log([A][HA])\text{pH} = p\text{K}_a + \log\left(\frac{[\text{A}^-]}{[\text{HA}]}\right)
pH=pKa+log(1)    pH=pKa\text{pH} = p\text{K}_a + \log(1) \implies \text{pH} = p\text{K}_a
5. Determine the approximate pKap\text{K}_a value from the titration curve: Find 10.0 mL10.0\text{ mL} on the horizontal axis (Volume of NaOH) and read the corresponding pH value on the vertical axis. The curve passes slightly below the 5.05.0 grid line, at a pH of approximately 4.7. Therefore:
pKa4.7p\text{K}_a \approx \mathbf{4.7}
Combining both pieces of information (pKa4.7p\text{K}_a \approx 4.7 and [NaOH]=0.10 M[\text{NaOH}] = 0.10\text{ M}), we confirm that Option B is the correct answer.

*

WHY_OTHERS_WRONG:

  • Option A is incorrect: While the pKap\text{K}_a of 4.74.7 is read correctly, the concentration of NaOH\text{NaOH} is calculated incorrectly as 0.050 M0.050\text{ M}. This error would occur if a student incorrectly assumed that only 10.0 mL10.0\text{ mL} (the half-equivalence volume) was required to reach the equivalence point, or if they made a dilution math error.
  • Option C is incorrect: A pKap\text{K}_a value of 9.39.3 represents the basic pH at (or slightly past) the equivalence point, rather than the pH at the half-equivalence point where pH=pKa\text{pH} = p\text{K}_a. Additionally, the concentration of NaOH\text{NaOH} is incorrectly calculated as 0.050 M0.050\text{ M}.
  • Option D is incorrect: While the concentration of NaOH\text{NaOH} of 0.10 M0.10\text{ M} is calculated correctly, the pKap\text{K}_a is incorrect. A value of 9.39.3 represents the basic pH at the equivalence point, not the pH at the half-equivalence point where pH=pKa\text{pH} = p\text{K}_a.
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