Making use of the assumptions we ordinarily make in calculating the \(\mathrm{pH}\) of an aqueous solution of a weak acid, calculate the \(\mathrm{pH}\) of a \(1.0 \times 10^{-6}-M\) solution of hypobromous acid (HBrO, \(K_{\mathrm{a}}=2 \times 10^{-9}\) ). What is wrong with your answer? Why is it wrong? Without trying to solve the problem, explain what has to be included to solve the problem correctly.

Short Answer

Expert verified
The calculated pH of a $1.0 \times 10^{-6}-M$ solution of hypobromous acid (HBrO) with $K_{a}=2 \times 10^{-9}$ is approximately 7.85. However, this is incorrect because it neglects the autoionization of water and its contribution to the [H+] concentration. To solve the problem correctly, we should take into account the autoionization of water (Kw = 1 x 10^{-14}) and add that to the [H+] due to HBrO ionization before calculating the pH.

Step by step solution

01

Write the weak acid ionization equation.

The ionization equation for hypobromous acid (HBrO) in water is: HBrO (aq) <=> H+ (aq) + BrO- (aq).
02

Write the expression for Ka.

The expression for Ka (acid dissociation constant) for HBrO is: Ka = \(\frac{[H^+][BrO^-]}{[HBrO]}\)
03

Set up initial and equilibrium concentrations molecule table (ICE table).

An ICE (Initial, Change, Equilibrium) table is used to set up the initial, changes that occur, and the equilibrium concentrations for all components of the ionization process. Initial concentrations of the components are: [HBrO] = 1.0 × 10^{-6} M [H+] = 0 M (assuming no dissociation initially) [BrO-] = 0 M (assuming no dissociation initially) During the ionization process, let 'x' be the change in concentration of H+. We then have the change in the concentrations as: [HBrO] -x [H+] +x [BrO-] +x Equilibrium concentrations are: [HBrO] = (1.0 × 10^{-6} - x) M [H+] = x M [BrO-] = x M
04

Substitute equilibrium concentrations into Ka expression and solve for x.

Plug the equilibrium concentrations of HBrO, H+, and BrO- into the Ka expression: Ka = 2 × 10^{-9} = \(\frac{x^2}{(1.0 × 10^{-6} - x)}\) Now, we assume that x is much smaller than the initial concentration of HBrO, so we simplify the equation as: 2 × 10^{-9} = \(\frac{x^2}{1.0 × 10^{-6}}\) Solve for x: x = \(\sqrt{(2 × 10^{-9})(1.0 × 10^{-6})}\) x = \(\sqrt{2 × 10^{-15}}\) x ≈ 1.4 × 10^{-8} M
05

Calculate the pH.

Since [H+] ≈ x, and pH = -log([H+]), therefore: pH = -log(1.4 × 10^{-8}) pH ≈ 7.85
06

What is wrong with our answer?

The assumption that the concentration of [H+] ions is solely due to the ionization of HBrO is wrong, as it neglects the autoionization of water. The [H+] ion concentration from water has to be taken into account since the HBrO concentration is very close to water autoionization equilibrium concentration.
07

How to solve the problem correctly?

To correctly calculate the pH value in this situation, we should take into account the [H+] contribution from the autoionization of water (Kw = 1 x 10^{-14}) and add that to the [H+] due to HBrO ionization before calculating the pH. This ensures that we consider both sources of H+ ions and do not underestimate the actual pH value of the solution.

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