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Calculate the \(\mathrm{pH}\) and the concentrations of all species present \(\left(\mathrm{H}_{3} \mathrm{O}^{+}, \mathrm{OH}, \mathrm{HIO}_{3}, \mathrm{IO}_{3}^{-}\right)\) in \(0.0500 \mathrm{M} \mathrm{HIO}_{3} . K_{a}\) for \(\mathrm{HIO}_{3}\) is \(1.7 \times 10^{-1}\)

Short Answer

Expert verified
pH ≈ 1.39; [H3O+] ≈ 0.0405 M; [IO3-] ≈ 0.0405 M; [HIO3] ≈ 0.0095 M; [OH-] ≈ 2.47 × 10^-13 M.

Step by step solution

01

Write the Dissociation Reaction

The dissociation reaction of \text{HIO}_3 in water is given by: \[\text{HIO}_3 + \text{H}_2\text{O} \rightleftharpoons \text{H}_3\text{O}^+ + \text{IO}_3^-\] Here, \(\text{HIO}_3\) dissociates to produce \(\text{H}_3\text{O}^+\) and \(\text{IO}_3^-\).
02

Set up the Expression for the Acid Dissociation Constant

The acid dissociation constant \(K_a\) for \(\text{HIO}_3\) is given by: \[K_a = \frac{[\text{H}_3\text{O}^+][\text{IO}_3^-]}{[\text{HIO}_3]}\] Given that \(K_a = 1.7 \times 10^{-1}\) and the initial concentration of \(\text{HIO}_3\) is 0.0500 M.
03

Define the Change in Concentrations

Assume \(x\) is the change in concentration at equilibrium. Initially, the concentration of \(\text{H}_3\text{O}^+\) and \(\text{IO}_3^-\) is 0. At equilibrium, \[[\text{H}_3\text{O}^+] = x, \quad [\text{IO}_3^-] = x, \quad [\text{HIO}_3] = 0.0500 - x\]
04

Solve for x Using the Quadratic Equation

Substitute the equilibrium concentrations into the \(K_a\) expression:\[1.7 \times 10^{-1} = \frac{x^2}{0.0500 - x}\]Solve this equation to find \(x\). Since this \(K_a\) is relatively large, we should not assume \(0.0500 - x \approx 0.0500\). This requires solving the quadratic equation:\[x^2 + 1.7x - 0.085 = 0\]Use the quadratic formula: \[x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}\]Substitute \(a = 1\), \(b = 1.7\), \(c = -0.085\):\[x = \frac{-1.7 \pm \sqrt{(1.7)^2 - 4(1)(-0.085)}}{2(1)}\]This gives \(x \approx 0.0405\).
05

Calculate \(\mathrm{pH}\) and Concentrations

Now that \(x\) is found to be 0.0405,- \([\text{H}_3\text{O}^+] = x \approx 0.0405 \text{ M}\)- \([\text{IO}_3^-] = x \approx 0.0405 \text{ M}\)- \([\text{HIO}_3] = 0.0500 - x = 0.0095 \text{ M}\)Calculate \(\mathrm{pH}\):\[\text{pH} = -\log[\text{H}_3\text{O}^+] = -\log(0.0405) \approx 1.39\]
06

Calculate Concentration of OH^-

Use the water autoionization constant \(K_w = 1.0 \times 10^{-14}\):\[K_w = [\text{H}_3\text{O}^+][\text{OH}^-]\]\[[\text{OH}^-] = \frac{1.0 \times 10^{-14}}{[\text{H}_3\text{O}^+]}\]Substitute \([\text{H}_3\text{O}^+]=0.0405\):\[[\text{OH}^-] = \frac{1.0 \times 10^{-14}}{0.0405} = 2.47 \times 10^{-13} \text{ M}\]

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Key Concepts

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

pH Calculation
When dealing with acids, understanding the concept of pH is essential. The pH scale is a measure of acidity or basicity in a solution. It's a logarithmic scale that runs from 0 to 14.
In our example, pH is determined from the concentration of hydronium ions (\[\text{H}_3\text{O}^+\]). The formula to calculate pH is:
  • \[\text{pH} = -\log{[\text{H}_3\text{O}^+]}\]
This means that a higher concentration of \[\text{H}_3\text{O}^+\] results in a lower pH, indicating a stronger acidic solution.
For instance, in the solution with \[\text{HIO}_3\] that dissociates to form \[\text{H}_3\text{O}^+\], we calculated \[\text{H}_3\text{O}^+\] to be 0.0405 M. Plugging this into the formula gives us a pH of approximately 1.39. This describes a strongly acidic environment, as pH values below 7 indicate acidity. Short recap:
  • Acids have pH values less than 7.
  • The more hydronium ions, the lower the pH value.
Acid-Base Equilibrium
Acid-base equilibrium describes the balance between the concentrations of acids and bases in a solution. When acids dissolve in water, they dissociate, releasing ions that establish equilibrium in the solution.
For the reaction \[\text{HIO}_3 + \text{H}_2\text{O} \rightleftharpoons \text{H}_3\text{O}^+ + \text{IO}_3^-\], the molecule \[\text{HIO}_3\] releases hydronium ions (\[\text{H}_3\text{O}^+\]) and iodate ions (\[\text{IO}_3^-\]).
This balance is described by the acid dissociation constant (\[K_a\]):
  • \[K_a = \frac{[\text{H}_3\text{O}^+][\text{IO}_3^-]}{[\text{HIO}_3]}\]

The value of \[K_a\] provides insight into the strength of an acid. A higher \[K_a\] indicates a stronger acid as it shows a greater extent of dissociation. In our exercise, \[K_a\] is given as\[1.7 \times 10^{-1}\], signifying significant dissociation, which supports the low pH found.
Key points:
  • Equilibrium implies the rate of acid dissociation equals the rate of association back into the acid form.
  • Changes in concentration affect the equilibrium, driven by Le Chatelier's Principle.
Quadratic Formula in Chemistry
The quadratic formula is a handy tool in chemistry, especially when dealing with equilibrium problems that involve squared terms. This comes into play when the acid dissociates, and the equilibrium expression involves a term squared.
In our solution for \[\text{HIO}_3\] dissociation, we derived the equation:
  • \[1.7 \times 10^{-1} = \frac{x^2}{0.0500 - x}\]
This leads to the quadratic form:
  • \[x^2 + 1.7x - 0.085 = 0\]
Using the quadratic formula to solve: \[x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}\] helps us find possible values for \[x\], the concentration at equilibrium. Using values \[a = 1\], \[b = 1.7\], and \[c = -0.085\], we found \[x\approx 0.0405\].
This is used to determine concentrations of equilibrium species. It is crucial when the simplification of assumptions (like neglecting \[x\] in the denominator) can't be applied.
Highlight:
  • The quadratic formula provides solutions in scenarios where the concentration changes are significant and assumptions aren't valid.
  • Understanding its use helps solve complex equilibrium problems in chemistry.

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Most popular questions from this chapter

The hydrated cation \(\mathrm{M}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{3+}\) has \(K_{\mathrm{a}}=10^{-4}\), and the acid \(\mathrm{HA}\) has \(K_{\mathrm{a}}=10^{-5}\). Identify the principal reaction in an aqueous solution of each of the following salts, and classify each solution as acidic, basic, or neutral: (a) \(\mathrm{NaA}\) (b) \(\mathrm{M}\left(\mathrm{NO}_{3}\right)_{3}\) (c) \(\mathrm{NaNO}_{3}\) (d) \(\mathrm{M} A_{3}\)

Which of the following can behave both as a Bronsted-Lowry acid and as a Bronsted-Lowry base? (a) \(\mathrm{HCO}_{3}^{-}\) (b) CN (c) \(\mathrm{H}_{2} \mathrm{O}\) (d) \(\mathrm{H}_{2} \mathrm{CO}_{3}\)

Write a balanced equation for the dissociation of each of the following Brønsted-Lowry acids in water: (a) \(\mathrm{H}_{2} \mathrm{SO}_{4}\) (b) \(\mathrm{HSO}_{4}^{-}\) (c) \(\mathrm{H}_{3} \mathrm{O}^{+}\) (d) \(\mathrm{NH}_{4}^{+}\) What is the conjugate base of each acid?

Acid and base behavior can be observed in solvents other than water. One commonly used solvent is dimethyl sulfoxide (DMSO), which can be treated as a monoprotic acid \({ }^{\circ}\) HSol." Just as water can behave cither as an acid or a base, so HSol can behave either as a Bronsted-Lowry acid or base. (a) The equilibrium constant for self-dissociation of HSol (call it \(K_{\text {HSel }}\) ) is \(1 \times 10^{-35}\). Write the chemical equation for the self- dissociation reaction and the corresponding equilibrium equation. (Hint: The equilibrium equation is analogous to the equilibrium equation for \(K_{w}\) in the case of water.) (b) The weak acid HCN has an acid dissociation constant \(K_{a}=1.3 \times 10^{-13}\) in the solvent HSol. If \(0.010 \mathrm{~mol}\) of \(\mathrm{NaCN}\) is dissolved in \(1.00 \mathrm{~L}\) of \(\mathrm{HSol}\), what is the equilibrium concentration of \(\mathrm{H}_{2} \mathrm{Sol}^{+}\) ?

The reaction of \(\mathrm{PCl}_{4}^{+}\) with \(\mathrm{Cl}^{-}\) is a Lewis acid- base reaction. Draw dectron-dot structures for the reactants and products, and use the curved arrow notation (Section 15.15) to represent the donation of a lone pair of electrons from the Lewis base to the Lewis acid.

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