The equilibrium constant for the following reaction is \(1.0 \times 10^{23}\). 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 \(0.0010 M\) in \(\mathrm{Cr}^{3+}\) and \(0.050 \mathrm{M}\) in \(\mathrm{H}_{2} \mathrm{EDTA}^{2-}\) and buffered at \(\mathrm{pH}=6.00 .\)

Short Answer

Expert verified
At equilibrium, the concentration of \(\mathrm{Cr^{3+}}\) ions in the solution is approximately \(0.0010\,\mathrm{M}\).

Step by step solution

01

Reaction Equation

\[\mathrm{Cr^{3+} + H_{2}EDTA^{2-} \rightleftharpoons Cr(EDTA)}\] We have the equilibrium constant Kc = 1.0 × 10²³ for this reaction. Now, let's write the expression for Kc:
02

Equilibrium Constant Expression

\[K_{c} = \frac{\left[\mathrm{Cr}\left(\mathrm{EDTA}\right)\right]}{\left[\mathrm{Cr^{3+}}\right]\left[\mathrm{H_{2}EDTA^{2-}}\right]}\] Next, we will set up an ICE (Initial, Change, Equilibrium) table for the reaction to find equilibrium concentrations:
03

ICE Table and Equilibrium Concentrations

ICE Table: Initial: \[ [\mathrm{Cr^{3+}}] = 0.0010\,\mathrm{M }\] \[ [\mathrm{H_{2}EDTA^{2-}}] = 0.050\,\mathrm{M} \] \[ [\mathrm{Cr(EDTA)}] = 0\,\mathrm{M} \] Change: \[ [\mathrm{Cr^{3+}}] = -x\,\mathrm{M} \] \[ [\mathrm{H_{2}EDTA^{2-}}] = -x\,\mathrm{M} \] \[ [\mathrm{Cr(EDTA)}] = +x\,\mathrm{M} \] Equilibrium: \[ [\mathrm{Cr^{3+}}] = (0.0010 - x)\,\mathrm{M} \] \[ [\mathrm{H_{2}EDTA^{2-}}] = (0.050 - x)\,\mathrm{M} \] \[ [\mathrm{Cr(EDTA)}] = x\,\mathrm{M} \] Now, we can substitute the equilibrium concentrations into the expression for Kc:
04

Substitution of Equilibrium Concentrations

\[\begin{aligned} 1.0 \times 10^{23} &= \frac{x}{(0.0010 - x)(0.050 - x)} \\ \end{aligned}\] Now, solve the equation for x:
05

Solving for x

Let's assume that the changes (x) are too small compared to the initial concentrations, meaning that the denominator remains essentially constant: \((0.0010)(0.050)\). This simplifies the expression as: \[1.0 \times 10^{23} = \frac{x}{(0.0010)(0.050)}\] Solving for x: \[x = 1.0 \times 10^{23} \times (0.0010)(0.050)\] \[x \approx 5.0 \times 10^{-22}\,\mathrm{M}\] Now that we have the value of x, we can find the equilibrium concentration of Cr^3+:
06

Calculating Equilibrium Concentration of Cr^3+

\[[\mathrm{Cr^{3+}}]_{equilibrium} = 0.0010 - x\] \[[\mathrm{Cr^{3+}}]_{equilibrium} = 0.0010 - 5.0 \times 10^{-22}\] \[[\mathrm{Cr^{3+}}]_{equilibrium} \approx 0.0010\,\mathrm{M}\] So, at equilibrium, the concentration of Cr^3+ ions in the solution is approximately 0.0010 M.

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Most popular questions from this chapter

Write equations for the stepwise formation of each of the following complex ions. a. \(\mathrm{CoF}_{6}^{3-}\) b. \(\mathrm{Zn}\left(\mathrm{NH}_{3}\right)_{4}^{2+}\)

a. Using the \(K_{\mathrm{sp}}\) value for \(\mathrm{Cu}(\mathrm{OH})_{2}\left(1.6 \times 10^{-19}\right)\) and the overall formation constant for \(\mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+}\left(1.0 \times 10^{13}\right)\), calculate the value for the equilibrium constant for the following reaction: \(\mathrm{Cu}(\mathrm{OH})_{2}(s)+4 \mathrm{NH}_{3}(a q) \rightleftharpoons \mathrm{Cu}\left(\mathrm{NH}_{3}\right)_{4}^{2+}(a q)+2 \mathrm{OH}^{-}(a q)\) b. Use the value of the equilibrium constant you calculated in part a to calculate the solubility (in \(\mathrm{mol} / \mathrm{L}\) ) of \(\mathrm{Cu}(\mathrm{OH})_{2}\) in \(5.0 \mathrm{M}\) \(\mathrm{NH}_{3} .\) In \(5.0 \mathrm{M} \mathrm{NH}_{3}\) the concentration of \(\mathrm{OH}^{-}\) is \(0.0095 \mathrm{M} .\)

When aqueous KI is added gradually to mercury(II) nitrate, an orange precipitate forms. Continued addition of KI causes the precipitate to dissolve. Write balanced equations to explain these observations. (Hint: \(\mathrm{Hg}^{2+}\) reacts with \(\mathrm{I}^{-}\) to form \(\mathrm{HgI}_{4}{ }^{2-}\).)

Calculate the solubility of each of the following compounds in moles per liter. Ignore any acid-base properties. a. \(\mathrm{Ag}_{3} \mathrm{PO}_{4}, K_{\mathrm{sp}}=1.8 \times 10^{-18}\) b. \(\mathrm{CaCO}_{3}, K_{\mathrm{sp}}=8.7 \times 10^{-9}\) c. \(\mathrm{Hg}_{2} \mathrm{Cl}_{2}, K_{\mathrm{sp}}=1.1 \times 10^{-18}\left(\mathrm{Hg}_{2}^{2+}\right.\) is the cation in solution.)

Sodium tripolyphosphate \(\left(\mathrm{Na}_{5} \mathrm{P}_{3} \mathrm{O}_{10}\right)\) is used in many synthetic detergents. Its major effect is to soften the water by complexing \(\mathrm{Mg}^{2+}\) and \(\mathrm{Ca}^{2+}\) ions. It also increases the efficiency of surfactants, or wetting agents that lower a liquid's surface tension. The \(K\) value for the formation of \(\mathrm{MgP}_{3} \mathrm{O}_{10}^{3-}\) is \(4.0 \times 10^{8} .\) The reaction is \(\mathrm{Mg}^{2+}+\mathrm{P}_{3} \mathrm{O}_{10}^{5-} \rightleftharpoons \mathrm{MgP}_{3} \mathrm{O}_{10}{ }^{3-} .\) Calculate the concentration of \(\mathrm{Mg}^{2+}\) in a solution that was originally \(50 . \mathrm{ppm} \mathrm{Mg}^{2+}(50 . \mathrm{mg} / \mathrm{L}\) of solution) after 40. g \(\mathrm{Na}_{5} \mathrm{P}_{3} \mathrm{O}_{10}\) is added to \(1.0 \mathrm{~L}\) of the solution.

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