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How do we measure and control the acidity of a solution?

The Bronsted-Lowry theory, the pH scale, strong and weak acids, Ka and Kw, titration curves, indicator choice and the action of buffer solutions.

An Edexcel 9CH0 Topic 17 answer covering the Bronsted-Lowry theory, the pH scale, strong and weak acids, Ka and Kw, titration curves, indicators and buffers.

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What this topic is asking

Edexcel Topic 17 wants you to apply the Bronsted-Lowry theory, calculate pH for strong and weak acids and bases using KaK_a, KwK_w and pKa\text{p}K_a, interpret titration curves, choose suitable indicators, and explain and calculate the action of buffer solutions.

The answer

Bronsted-Lowry theory and pH

Strong and weak acids

For a strong acid such as HCl\text{HCl} (full dissociation), [H+][\text{H}^+] equals the acid concentration, so the pH follows directly. For a weak acid (partial dissociation), use the acid dissociation constant:

The ionic product of water is Kw=[H+][OH]=1.0×1014 mol2dm6K_w = [\text{H}^+][\text{OH}^-] = 1.0 \times 10^{-14}\ \text{mol}^2\,\text{dm}^{-6} at 298 K298\ \text{K}. For a strong base, find [OH][\text{OH}^-] from the concentration, then use [H+]=Kw/[OH][\text{H}^+] = K_w / [\text{OH}^-] to get the pH.

Titration curves and indicators

Buffer solutions

To calculate a buffer pH, rearrange the KaK_a expression to [H+]=Ka×[HA][A][\text{H}^+] = K_a \times \dfrac{[\text{HA}]}{[\text{A}^-]}. At the half-equivalence point of a weak-acid titration, [HA]=[A][\text{HA}] = [\text{A}^-], so [H+]=Ka[\text{H}^+] = K_a and pH=pKa\text{pH} = \text{p}K_a, a useful way to find KaK_a from a curve.

Examples in context

Example 1. Blood as a buffer. Human blood is buffered at about pH 7.47.4 by the carbonic acid / hydrogencarbonate system, H2CO3H++HCO3\text{H}_2\text{CO}_3 \rightleftharpoons \text{H}^+ + \text{HCO}_3^-. Added acid is removed by HCO3\text{HCO}_3^- and added base by H2CO3\text{H}_2\text{CO}_3, while the lungs and kidneys adjust the components. This is exactly the acidic-buffer action of Topic 17, and a deviation of even 0.40.4 pH units can be life-threatening, showing why buffering is biologically vital.

Example 2. Choosing the indicator for an ethanoic acid titration. When standardising sodium hydroxide against ethanoic acid (a weak acid with a strong base), the equivalence point lies above pH 77 because the salt formed is slightly alkaline. Phenolphthalein (range 8.38.3 to 1010) changes colour within the steep section, giving a sharp end point, whereas methyl orange would change far too early. Picking the indicator to match the curve is a routine but heavily marked skill.

Try this

Q1. Calculate the pH of 0.010 mol dm30.010\ \text{mol dm}^{-3} hydrochloric acid. [1 mark]

  • Cue. Strong acid, [H+]=0.010[H^+] = 0.010; pH=log10(0.010)=2.00\text{pH} = -\log_{10}(0.010) = 2.00.

Q2. Explain how an acidic buffer resists a rise in pH when a small amount of alkali is added. [2 marks]

  • Cue. The weak acid reacts with the added OHOH^-, removing it and keeping [H+][H^+] approximately constant.

Exam-style practice questions

Practice questions written in the style of Pearson Edexcel exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

Edexcel 20194 marksCalculate the pH of 0.150 mol dm30.150\ \text{mol dm}^{-3} ethanoic acid. (Ka=1.74×105 mol dm3K_a = 1.74 \times 10^{-5}\ \text{mol dm}^{-3}.) State one assumption you make.
Show worked answer →

Use the weak-acid approximation and take logs.

For a weak acid, Ka=[H+]2[HA]K_a = \dfrac{[\text{H}^+]^2}{[\text{HA}]} assuming [H+]=[A][\text{H}^+] = [\text{A}^-] and that dissociation is small so [HA][\text{HA}] stays at 0.1500.150 (1, assumption).

[H+]=Ka×[HA]=1.74×105×0.150=2.61×106=1.62×103 mol dm3[\text{H}^+] = \sqrt{K_a \times [\text{HA}]} = \sqrt{1.74 \times 10^{-5} \times 0.150} = \sqrt{2.61 \times 10^{-6}} = 1.62 \times 10^{-3}\ \text{mol dm}^{-3} (2).

pH=log10(1.62×103)=2.79\text{pH} = -\log_{10}(1.62 \times 10^{-3}) = 2.79 (1).

Markers reward the correct rearrangement, value of [H+][\text{H}^+], and pH to 2 decimal places, plus a stated assumption.

Edexcel 20215 marksA buffer is made by dissolving 0.20 mol0.20\ \text{mol} of sodium ethanoate in 1.0 dm31.0\ \text{dm}^3 of 0.10 mol dm30.10\ \text{mol dm}^{-3} ethanoic acid. (Ka=1.74×105K_a = 1.74 \times 10^{-5}.) (a) Calculate the pH. (b) Explain how the buffer resists a rise in pH when a little alkali is added.
Show worked answer →

Use the buffer expression, then explain the equilibrium response.

(a) Ka=[H+][A][HA]K_a = [\text{H}^+]\dfrac{[\text{A}^-]}{[\text{HA}]}, so [H+]=Ka[HA][A]=1.74×105×0.100.20=8.7×106 mol dm3[\text{H}^+] = K_a \dfrac{[\text{HA}]}{[\text{A}^-]} = 1.74 \times 10^{-5} \times \dfrac{0.10}{0.20} = 8.7 \times 10^{-6}\ \text{mol dm}^{-3} (2). pH=log10(8.7×106)=5.06\text{pH} = -\log_{10}(8.7 \times 10^{-6}) = 5.06 (1).

(b) Added OH\text{OH}^- reacts with the weak acid CH3COOH\text{CH}_3\text{COOH} (the reservoir): CH3COOH+OHCH3COO+H2O\text{CH}_3\text{COOH} + \text{OH}^- \rightarrow \text{CH}_3\text{COO}^- + \text{H}_2\text{O} (1), so [H+][\text{H}^+] and hence pH change only slightly (1).

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