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The amount of iron in a meteorite is determined by a redox titration using \(\mathrm{KMnO}_{4}\) as the titrant. A \(0.4185-\mathrm{g}\) sample is dissolved in acid and the liberated \(\mathrm{Fe}^{3+}\) quantitatively reduced to \(\mathrm{Fe}^{2+}\) using a Walden reductor. Titrating with \(0.02500 \mathrm{M} \mathrm{KMnO}_{4}\) requires \(41.27 \mathrm{~mL}\) to reach the end point. Determine the \(\% \mathrm{w} / \mathrm{w} \mathrm{Fe}_{2} \mathrm{O}_{3}\) in the sample of meteorite.

Short Answer

Expert verified
The sample is 98.47% \(\text{Fe}_2\text{O}_3\) by mass.

Step by step solution

01

Write the Balanced Equation

Start by recognizing the redox reaction: \[ 5 ext{Fe}^{2+} + ext{MnO}_4^{-} + 8 ext{H}^{+} \rightarrow 5 ext{Fe}^{3+} + ext{Mn}^{2+} + 4 ext{H}_2 ext{O} \] This equation shows that 5 moles of \(\text{Fe}^{2+}\) react with 1 mole of \(\text{MnO}_4^{-}\).
02

Calculate Moles of Permanganate Used

Find the moles of \(\text{KMnO}_4\) used in the titration:\[ moles = M \times V = 0.02500 \,\text{mol/L} \times 0.04127 \,\text{L} \approx 1.03175 \times 10^{-3} \,\text{mol} \] This is the number of moles of \(\text{KMnO}_4\) used.
03

Determine Moles of Iron

Use the stoichiometry from the balanced equation to determine moles of \(\text{Fe}^{2+}\):\[ 5 \text{moles of Fe}^{2+} \text{ per 1 mole of MnO}_4^{-}\ herefore moles = 5 \times 1.03175 \times 10^{-3} \ approx 5.15875 \times 10^{-3} \,\text{mol Fe}^{2+} \].
04

Convert Moles of Iron to Mass of Fe2O3

First, convert moles of \(\text{Fe}^{2+}\) to moles of \(\text{Fe}_2\text{O}_3\):\[ 2 \text{Fe}^{3+} \text{ form 1 } \text{Fe}_2\text{O}_3 \Rightarrow moles \; \text{Fe}_2\text{O}_3 = \frac{5.15875 \times 10^{-3}}{2} approx 2.57938 \times 10^{-3} \,\text{mol Fe}_2\text{O}_3 \]Now calculate the mass:\[ Molar \,\text{mass} \,\text{Fe}_2\text{O}_3 = 2(55.85) + 3(16.00) = 159.7 \,\text{g/mol} \]\[ \text{mass} = 2.57938 \times 10^{-3} \,\text{mol} \times 159.7 \/\text{g/mol} approx 0.4121 \,\text{g Fe}_2\text{O}_3 \]
05

Calculate Percentage of Fe2O3 in Sample

Calculate the percentage of \(\text{Fe}_2\text{O}_3\) in the sample:\[ \% \,\text{w/w} \,\text{Fe}_2\text{O}_3 = \left( \frac{0.4121 \,\text{g Fe}_2\text{O}_3}{0.4185 \,\text{g sample}} \right) \times 100 \approx 98.47\% \] This percentage represents the mass fraction of \(\text{Fe}_2\text{O}_3\) in the meteorite sample.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Stoichiometry
Stoichiometry is the branch of chemistry that deals with the quantitative relationships between reactants and products in a chemical reaction. It's like a recipe in cooking, detailing the exact amount of each ingredient needed to make the desired dish. In the context of our exercise, stoichiometry helps determine how much of one substance (the titrant) is needed to react completely with another substance (the analyte).

Redox titration involves a specific stoichiometric relationship between oxidizing and reducing agents. For instance, in our exercise, the balanced equation tells us that 5 moles of iron(II) ions (\(\mathrm{Fe}^{2+}\)) react with 1 mole of permanganate ions (\(\mathrm{MnO}_4^-\)). This 5:1 ratio is crucial for accurately calculating the amount of iron present in a sample based on the volume and concentration of \(\mathrm{KMnO}_4\) used in the titration. Understanding stoichiometry ensures that chemists use just the right amount of chemicals to achieve complete reactions.
Balanced equation
A balanced equation is fundamental in chemistry to represent accurately the transformation that occurs in a reaction. In a balanced equation, the number of atoms for each element is the same on both sides of the equation, ensuring that matter is conserved.

Consider the given equation: \[ 5 \,\mathrm{Fe}^{2+} + \mathrm{MnO}_4^{-} + 8 \,\mathrm{H}^{+} \rightarrow 5 \,\mathrm{Fe}^{3+} + \mathrm{Mn}^{2+} + 4 \,\mathrm{H}_2\mathrm{O} \]. This equation shows how iron(II) ions react with permanganate ions under acidic conditions. By balancing this equation, we determine the exact ratios of reactants and products. Here, every part of the reaction—iron(II), permanganate, hydronium, and the resultant iron(III), manganese(II), and water—fits together perfectly to ensure conservation of mass. Without a balanced equation, we would not know how many moles of one substance react with another, making accurate calculations impossible.
Molar mass
Molar mass is a critical concept that relates the mass of a substance to the amount of substance measured in moles. It's essentially the weight of one mole of a given substance, typically expressed in grams per mole (g/mol).

In our exercise, the molar mass of iron(III) oxide (\(\mathrm{Fe}_2\mathrm{O}_3\)) is used to convert moles back into grams. Calculating the molar mass involves summing the atomic masses of all atoms in a formula: \(2 \times 55.85 + 3 \times 16.00 = 159.7 \,\mathrm{g/mol}\) for \(\mathrm{Fe}_2\mathrm{O}_3\).

This value helps transform the moles of \(\mathrm{Fe}_2\mathrm{O}_3\) computed from the reaction stoichiometry back into grams. The mass calculation is necessary when determining the weight percentage of iron oxide in the sample. This bridge from moles to grams is a quintessential part of chemical quantification, linking reactants to measurable amounts.
Iron oxidation states
In chemistry, an oxidation state, often called an oxidation number, signifies the degree of oxidation of an atom in a chemical compound. For iron, common oxidation states are +2 and +3, referred to as ferrous and ferric states, respectively.

During titrations like the one in our example, iron changes its oxidation state through a redox reaction. The iron in the sample starts as \(\mathrm{Fe}^{3+}\), and is reduced to \(\mathrm{Fe}^{2+}\) by a reductor before titration. The \(\mathrm{KMnO}_4\) in turn oxidizes \(\mathrm{Fe}^{2+}\) back to \(\mathrm{Fe}^{3+}\) during the titration process.

Understanding the change in oxidation states is essential as they underpin the stoichiometry of the reaction. Each change in the oxidation state indicates electron transfer, crucial for calculating the equivalence point in titrations. Thus, recognizing and differentiating between these states allows chemists to track and quantify the progress of a reaction accurately.

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Most popular questions from this chapter

The concentration of \(\mathrm{SO}_{2}\) in air is determined by bubbling a sample of air through a trap that contains \(\mathrm{H}_{2} \mathrm{O}_{2} .\) Oxidation of \(\mathrm{SO}_{2}\) by \(\mathrm{H}_{2} \mathrm{O}_{2}\) results in the formation of \(\mathrm{H}_{2} \mathrm{SO}_{4}\), which is then determined by titrating with \(\mathrm{NaOH}\). In a typical analysis, a sample of air is passed through the peroxide trap at a rate of \(12.5 \mathrm{~L} / \mathrm{min}\) for \(60 \mathrm{~min}\) and required \(10.08 \mathrm{~mL}\) of \(0.0244 \mathrm{M} \mathrm{NaOH}\) to reach the phenolphthalein end point. Calculate the \(\mu \mathrm{L} / \mathrm{L} \mathrm{SO}_{2}\) in the sample of air. The density of \(\mathrm{SO}_{2}\) at the temperature of the air sample is \(2.86 \mathrm{mg} / \mathrm{mL}\).

Explain why it is not possible for a sample of water to simultaneously have \(\mathrm{OH}^{-}\) and \(\mathrm{HCO}_{3}^{-}\) as sources of alkalinity.

Before the introduction of EDTA most complexation titrations used \(\mathrm{Ag}^{+}\) or \(\mathrm{CN}^{-}\) as the titrant. The analysis for \(\mathrm{Cd}^{2+},\) for example, was accomplished indirectly by adding an excess of \(\mathrm{KCN}\) to form \(\mathrm{Cd}(\mathrm{CN})_{4}^{2-}\), and back titrating the excess \(\mathrm{CN}^{-}\) with \(\mathrm{Ag}^{+},\) forming \(\mathrm{Ag}(\mathrm{CN})_{2}^{-} .\) In one such analysis a \(0.3000-\mathrm{g}\) sample of an ore is dissolved and treated with \(20.00 \mathrm{~mL}\) of \(0.5000 \mathrm{M} \mathrm{KCN}\). The excess \(\mathrm{CN}^{-}\) requires \(13.98 \mathrm{~mL}\) of \(0.1518 \mathrm{M} \mathrm{AgNO}_{3}\) to reach the end point. Determine the \(\% \mathrm{w} / \mathrm{w}\) Cd in the ore.

The concentration of cyanide, \(\mathrm{CN}^{-},\) in a copper electroplating bath is determined by a complexometric titration using \(\mathrm{Ag}^{+}\) as the titrant, forming the soluble \(\mathrm{Ag}(\mathrm{CN})_{2}^{-}\) complex. In a typical analysis a \(5.00-\mathrm{mL}\) sample from an electroplating bath is transferred to a 250 -mL Erlenmeyer flask, and treated with \(100 \mathrm{~mL}\) of \(\mathrm{H}_{2} \mathrm{O}, 5 \mathrm{~mL}\) of \(20 \% \mathrm{w} / \mathrm{v}\) \(\mathrm{NaOH}\) and \(5 \mathrm{~mL}\) of \(10 \% \mathrm{w} / \mathrm{v}\) KI. The sample is titrated with 0.1012 \(\mathrm{M} \mathrm{AgNO}_{3}\), requiring \(27.36 \mathrm{~mL}\) to reach the end point as signaled by the formation of a yellow precipitate of AgI. Report the concentration of cyanide as parts per million of \(\mathrm{NaCN}\).

The amount of calcium in physiological fluids is determined by a complexometric titration with EDTA. In one such analysis a \(0.100-\mathrm{mL}\) sample of a blood serum is made basic by adding 2 drops of \(\mathrm{NaOH}\) and titrated with \(0.00119 \mathrm{M}\) EDTA, requiring \(0.268 \mathrm{~mL}\) to reach the end point. Report the concentration of calcium in the sample as milligrams Ca per \(100 \mathrm{~mL}\).

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