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Fe3+(aq) + KSCN(s) → FeSCN2+(aq) + K+(aq) 5. To determine the moles of Fe3+(aq) in a 100. mL sample Solutions Chemistry Question

Question

Fe3+(aq) + KSCN(s) → FeSCN2+(aq) + K+(aq)

  1. To determine the moles of Fe3+(aq) in a 100. mL sample of an unknown solution, excess KSCN(s) is added to convert all the Fe3+(aq) into the dark red species FeSCN2+(aq), as represented by the equation above. The absorbance of FeSCN2+(aq) at different concentrations is shown in the graph below.

[VISUAL]

If the absorbance of the mixture is 0.20 at 453 nm, how many moles of Fe3+(aq) were present in the 100. mL sample? (Assume that any volume change due to adding the KSCN(s) is negligible.)

A.

4 × 10^−4 mol

B.

3 × 10^−4 mol

C.

4 × 10^−6 mol

✓ Correct
D.

3 × 10^−6 mol

💡 Solution & Explanation

STEPS:

1. Understand the core analytical concept (Beer's Law): The graph provided is a calibration curve that relates the absorbance (AA) of the dark-red coordination complex FeSCN2+\text{FeSCN}^{2+} to its molar concentration (MM) at a specific wavelength (453 nm). According to the Beer-Lambert Law, absorbance is directly proportional to concentration (A=ϵbCA = \epsilon bC), yielding a straight line of best fit passing through the origin.
2. Read the concentration of FeSCN2+\text{FeSCN}^{2+} from the best-fit line:
* Locate 0.200.20 on the y-axis (Absorbance at 453 nm).
* Follow the grid line horizontally to the right until it intersects the solid line of best fit.
* From that intersection point, look vertically downward to read the concentration on the x-axis.
* The intersection lies exactly on the fourth grid line, which corresponds to a concentration of 4.0×105 M4.0 \times 10^{-5}\text{ M} (since the major grid line is 5×105 M5 \times 10^{-5}\text{ M} and has 5 subdivisions, each vertical grid line represents exactly 1.0×105 M1.0 \times 10^{-5}\text{ M}).
3. Apply the stoichiometry of the complexation reaction:
* Look at the balanced chemical equation representing the conversion:
Fe3+(aq)+KSCN(s)FeSCN2+(aq)+K+(aq)\text{Fe}^{3+}(aq) + \text{KSCN}(s) \rightarrow \text{FeSCN}^{2+}(aq) + \text{K}^+(aq)
* Because an excess of solid KSCN\text{KSCN} is added, the iron(III) ion (Fe3+\text{Fe}^{3+}) is the limiting reactant and is completely converted into FeSCN2+\text{FeSCN}^{2+}.
* The stoichiometric ratio between Fe3+\text{Fe}^{3+} and FeSCN2+\text{FeSCN}^{2+} is exactly 1:11:1. Therefore:
Moles of Fe3+ initially present=Moles of FeSCN2+ produced\text{Moles of Fe}^{3+}\text{ initially present} = \text{Moles of FeSCN}^{2+}\text{ produced}
4. Convert the sample volume to liters:
* The volume of the sample is 100. mL100.\text{ mL}.
* Converting to liters (L\text{L}) gives:
100. mL×1 L1000 mL=0.100 L100.\text{ mL} \times \frac{1\text{ L}}{1000\text{ mL}} = \mathbf{0.100\text{ L}}
5. Calculate the moles of Fe3+\text{Fe}^{3+} present:
* Use the molarity equation (n=M×Vn = M \times V) to find the total moles in the sample:
Moles of FeSCN2+=(4.0×105 mol/L)×(0.100 L)=4.0×106 mol\text{Moles of FeSCN}^{2+} = (4.0 \times 10^{-5}\text{ mol/L}) \times (0.100\text{ L}) = \mathbf{4.0 \times 10^{-6}\text{ mol}}
* Since there is a 1:1 ratio, the initial moles of Fe3+\text{Fe}^{3+} are exactly 4×106 mol4 \times 10^{-6}\text{ mol}, which identifies Option C as the correct answer.

*

WHY_OTHERS_WRONG:

  • Option A is incorrect (4×104 mol4 \times 10^{-4}\text{ mol}): This value is off by two orders of magnitude. A student might arrive at this option if they read the concentration correctly as 4.0×105 M4.0 \times 10^{-5}\text{ M} but made a decimal error when converting 100. mL100.\text{ mL} to liters (e.g., multiplying by 10 instead of dividing by 1000).
  • Option B is incorrect (3×104 mol3 \times 10^{-4}\text{ mol}): This option is off in both the coefficient and the exponent. It represents a combination of a misread concentration value (reading an outlier data point instead of the best-fit line) and a metric conversion/mathematical mistake.
  • Option D is incorrect (3×106 mol3 \times 10^{-6}\text{ mol}): A student will arrive at this incorrect answer if they read the coordinate of the individual experimental data point closest to an absorbance of 0.20 (which sits near 3.0×105 M3.0 \times 10^{-5}\text{ M}) rather than reading from the solid line of best fit (which is at 4.0×105 M4.0 \times 10^{-5}\text{ M}). When performing calibration curve calculations in science, values must always be determined using the calibrated line of best fit rather than raw, unadjusted data points.
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