The equilibrium constant for the following reaction is \(1.0 \times 10^{23}:\) $$\mathrm{Cr}^{3+}(a q)+\mathrm{H}_{2} \mathrm{EDTA}^{2-}(a q) \rightleftharpoons \mathrm{CrEDTA}^{-}(a q)+2 \mathrm{H}^{+}(a q)$$ EDTA is used as a complexing agent in chemical analysis. Solutions of EDTA, usually containing the disodium salt \(\mathrm{Na}_{2} \mathrm{H}_{2} \mathrm{EDTA},\) are used to treat heavy metal poisoning. Calculate \(\left[\mathrm{Cr}^{3+}\right]\) at equilibrium in a solution originally \(0.0010 \mathrm{M}\) in \(\mathrm{Cr}^{3+}\) and \(0.050 M\) in \(\mathrm{H}_{2} \mathrm{EDTA}^{2-}\) and buffered at \(\mathrm{pH}=6.00\).

Short Answer

Expert verified
The equilibrium concentration of Cr³⁺ in the given solution is approximately 0.0010 M.

Step by step solution

01

Write down the balanced chemical equation and the expression for the equilibrium constant

First, we need to write down the balanced chemical equation given in the exercise: \[\mathrm{Cr}^{3+}(a q)+\mathrm{H}_{2} \mathrm{EDTA}^{2-}(a q) \rightleftharpoons \mathrm{CrEDTA}^{-}(a q)+2 \mathrm{H}^{+}(a q)\] Then, we write the expression for the equilibrium constant, \(K_{eq}\): \[K_{eq} = \frac{[\mathrm{CrEDTA}^{-}][\mathrm{H^{+}}]^{2}}{[\mathrm{Cr}^{3+}][\mathrm{H}_{2}\mathrm{EDTA}^{2-}]}\] The equilibrium constant value is given as \(1.0 \times 10^{23}\).
02

Set up a RICE (Reaction, Initial, Change, Equilibrium) table to keep track of the concentrations

In order to keep track of the concentrations of each species during the reaction, we can set up a RICE table: | | Cr³⁺ | H₂EDTA²⁻ | CrEDTA⁻ | H⁺ | |------|------|--------|--------|----| | R | | | | | | I | 0.0010 | 0.050 | 0 | \(10^{-6}\) | | C | -x | -x | +x | +2x | | E |0.0010 - x | 0.050 - x | x | \(10^{-6}\) + 2x | Here, RICE stands for Reaction, Initial, Change, and Equilibrium. The initial concentrations of Cr³⁺ and H₂EDTA²⁻ are given as 0.0010 M and 0.050 M, respectively. The initial concentration of CrEDTA⁻ is 0 M, as it has not formed yet. Since the pH is given as 6.00, we know that the initial concentration of H⁺ = \(10^{-6}\) M. During the reaction, the concentrations of the reactants Cr³⁺ and H₂EDTA²⁻ will decrease by an amount x and the concentrations of the products CrEDTA⁻ and H⁺ will increase by x and 2x, respectively.
03

Substitute the equilibrium concentrations into the equilibrium constant expression

Now we can substitute the equilibrium concentrations given in the RICE table into the expression for the equilibrium constant: \begin{align*} 1.0 \times 10^{23} &= \frac{(x)[10^{-6} + 2x]^{2}}{(0.0010 - x)(0.050 - x)} \end{align*} Since \(K_{eq}\) is very large, we can assume that the reaction will go almost to completion, so x is close to the initial concentration of Cr³⁺ (0.0010 M). Therefore, we can simplify the expression by assuming that \(0.0010 - x \approx 0.0010\) and \(0.050 - x \approx 0.050\): \begin{align*} 1.0 \times 10^{23} &\approx \frac{(x)[10^{-6} + 2x]^{2}}{(0.0010)(0.050)} \end{align*}
04

Solve for x (the concentration of CrEDTA⁻ at equilibrium)

Now we need to solve the simplified equation for x: \begin{align*} x[10^{-6} + 2x]^{2} &= 1.0 \times 10^{23} \times 0.0010 \times 0.050 \\ x(10^{-6} + 2x)^{2}& \approx 5.0 \times 10^{20} \end{align*} To simplify the equation, we can also assume that \(2x \ll 10^{-6}\) since the value of x will be very small compared to \(10^{-6}\). This results in: \begin{align*} x(10^{-6})^2 &\approx 5.0 \times 10^{20} \\ x &\approx \frac{5.0 \times 10^{20}}{(10^{-6})^{2}} \\ x &\approx 5.0 \times 10^{-8} \end{align*}
05

Determine the equilibrium concentration of Cr³⁺

We know that the equilibrium concentration of Cr³⁺ is given by \(0.0010 - x\), so: \[[\mathrm{Cr}^{3+}]_{eq} = 0.0010 - 5.0 \times 10^{-8} \approx 0.0010\ \mathrm{M}\] Thus, the equilibrium concentration of Cr³⁺ is approximately 0.0010 M.

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Most popular questions from this chapter

A solution is prepared by adding 0.10 mole of \(\mathrm{Ni}\left(\mathrm{NH}_{3}\right)_{6} \mathrm{Cl}_{2}\) to \(0.50 \mathrm{L}\) of \(3.0 M \mathrm{NH}_{3} .\) Calculate \(\left[\mathrm{Ni}\left(\mathrm{NH}_{3}\right)_{6}^{2+}\right]\) and \(\left[\mathrm{Ni}^{2+}\right]\) in this solution. \(K_{\text {overall }}\) for \(\mathrm{Ni}\left(\mathrm{NH}_{3}\right)_{6}^{2+}\) is \(5.5 \times 10^{8} .\) That is, $$5.5 \times 10^{8}=\frac{\left[\mathrm{Ni}\left(\mathrm{NH}_{3}\right)_{6}^{2+}\right]}{\left[\mathrm{Ni}^{2+}\right]\left[\mathrm{NH}_{3}\right]^{6}}$$ for the overall reaction $$ \mathrm{Ni}^{2+}(a q)+6 \mathrm{NH}_{3}(a q) \rightleftharpoons \mathrm{Ni}\left(\mathrm{NH}_{3}\right)_{6}^{2+}(a q) $$

A solution is \(1 \times 10^{-4} M\) in \(\mathrm{NaF}, \mathrm{Na}_{2} \mathrm{S},\) and \(\mathrm{Na}_{3} \mathrm{PO}_{4} .\) What would be the order of precipitation as a source of \(\mathrm{Pb}^{2+}\) is added gradually to the solution? The relevant \(K_{\mathrm{sp}}\) values are \(K_{\mathrm{sp}}\left(\mathrm{PbF}_{2}\right)\) \(=4 \times 10^{-8}, K_{\mathrm{sp}}(\mathrm{PbS})=7 \times 10^{-29},\) and \(K_{\mathrm{sp}}\left[\mathrm{Pb}_{3}\left(\mathrm{PO}_{4}\right)_{2}\right]=\) \(1 \times 10^{-54}\).

Calculate the solubility of \(\mathrm{AgCN}(s)\left(K_{\mathrm{sp}}=2.2 \times 10^{-12}\right)\) in a solution containing \(1.0 M \mathrm{H}^{+} .\left(K_{\mathrm{a}} \text { for } \mathrm{HCN} \text { is } 6.2 \times 10^{-10} .\right)\)

In the presence of \(\mathrm{NH}_{3}, \mathrm{Cu}^{2+}\) forms the complex ion \(\mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+} .\) If the equilibrium concentrations of \(\mathrm{Cu}^{2+}\) and \(\mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+}\) are \(1.8 \times 10^{-17} M\) and \(1.0 \times 10^{-3} M,\) respectively, in a \(1.5-M \mathrm{NH}_{3}\) solution, calculate the value for the overall formation constant of \(\mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+}\). $$\mathrm{Cu}^{2+}(a q)+4 \mathrm{NH}_{3}(a q) \rightleftharpoons \mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+}(a q) \quad K_{\mathrm{overall}}=?$$

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