Ph Strong Acids Bases
Learn and apply Ph Strong Acids Bases in the published Chemistry course sequence.
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The core idea
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pH of Strong Acids and Strong Bases: Orientation
Treat pH as a concentration calculation with a logarithm at the end. Establish the ion stoichiometry before pressing calculator keys.
- Weak-acid and weak-base pH calculations are excluded from H1.
Definitions (Must Know)
- pH = −log10[H+], with [H+] in mol dm−3.
- For strong bases at 25 °C, find [OH−], use [H+] = Kw/[OH−], then calculate pH.
Detailed Explanations
A 0.0200 mol dm−3 strong monoprotic acid gives [H+] = 0.0200 mol dm−3, so pH = −log10(0.0200).
A 0.00500 mol dm−3 Ba(OH)2 solution gives [OH−] = 0.0100 mol dm−3. At 25 °C, [H+] = 1.0 × 10−12 mol dm−3 and pH = 12.00.
For a strong monoprotic acid, [H⁺] equals the analytical concentration. For a strong base, first obtain [OH⁻], calculate pOH, then use pH + pOH = 14 at 25 °C.
A coefficient in the dissociation equation can change ion concentration; it must not be ignored.
Worked Examples
Modelled example 1
Core application
Problem
Study the worked solution
Identify hydroxide concentration
Method
Use the one-to-one complete dissociation of sodium hydroxide.Reason
Each formula unit supplies one hydroxide ion.Working
[OH⁻] = 2.50 × 10⁻³ mol dm⁻³.Find hydrogen-ion concentration
Method
Rearrange K_w = [H⁺][OH⁻].Reason
The pH definition uses hydrogen-ion concentration.Working
[H⁺] = (1.0 × 10⁻¹⁴)/(2.50 × 10⁻³) = 4.00 × 10⁻¹² mol dm⁻³.Calculate pH
Method
Take the negative logarithm of [H⁺].Reason
pH = - log ₁₀[H⁺].Working
pH = 11.40.
Guided practice 2
Strong-base pH with stoichiometry
Problem
Try this before viewing the solution
Hints
Hint 1: formula coefficient
Hint 2: base scale
View solution step by step
Apply dissociation stoichiometry
Method
Double the formula-unit concentration.Reason
Ba(OH)₂ → Ba²⁺ + 2OH⁻.Working
[OH⁻] = 2(0.0050) = 0.010 mol dm⁻³.Calculate pOH
Method
Take - log ₁₀[OH⁻].Reason
Hydroxide concentration maps directly to pOH.Working
pOH = 2.00.Convert to pH
Method
Subtract pOH from pK_w.Reason
The sum is fixed by the stated temperature-specific water constant.Working
pH = 14.00-2.00 = 12.00.
Common misconception 3
Distinguish pOH from pH
Learner result
Choose the quantity calculated
View solution step by step
Name the logarithmic scale
Method
Label - log ₁₀[OH⁻] as pOH.Reason
pH is defined from [H⁺] instead.Working
pOH = 2.00.Convert at the stated temperature
Method
Use pH = pK_w-pOH.Reason
At 25°C the supplied pK_w is 14.00.Working
pH = 14.00-2.00 = 12.00.
Examiner practice 4
Dilute before taking the logarithm
Problem
Try this before viewing the solution
View solution step by step
Find dilution factor
1 markMethod
Compare initial aliquot with final volume.Reason
The amount of acid is unchanged while volume increases tenfold.Working
25.0/250.0 = 0.100.Find final concentration
1 markMethod
Multiply by the volume ratio.Reason
c₁V₁ = c₂V₂.Working
c₂ = 0.200(0.100) = 0.0200 mol dm⁻³.Relate acid to hydrogen ions
1 markMethod
Use the one-to-one strong monoprotic model.Reason
Nitric acid supplies one proton per formula unit under complete dissociation.Working
[H⁺] = 0.0200 mol dm⁻³.Calculate pH
1 markMethod
Apply the negative logarithm after dilution.Reason
The pH depends on final, not stock, concentration.Working
pH = - log ₁₀(0.0200) = 1.70.
Self-mark with the mark scheme
Compare your response with each mark point. Select a point only when your response contains that evidence.
Credit the dilution ratio, final concentration, hydrogen-ion relation and pH.
Challenge 5
Find pH after partial neutralisation
Problem
Try this before viewing the solution
Hints
Hint 1: react amounts first
Hint 2: use total volume
View solution step by step
Calculate reacting amounts
Method
Find moles of acid and base.Reason
Neutralisation is a one-to-one reaction between H⁺ and OH⁻.Working
n(H⁺) = 0.100(0.0250) = 2.50 × 10⁻³ mol; n(OH⁻) = 0.100(0.0150) = 1.50 × 10⁻³ mol.Find excess concentration
Method
Subtract base moles and divide excess acid by total volume.Reason
The remaining hydrogen ions occupy the combined solution.Working
[H⁺] = (1.00 × 10⁻³)/0.0400 = 0.0250 mol dm⁻³.Calculate final pH
Method
Take the negative logarithm of the excess hydrogen-ion concentration.Reason
Neutralisation and mixing have already established the final concentration.Working
pH = - log ₁₀(0.0250) = 1.60.
Mind Stretchers
Attempt the independent prompts before opening a hint or solution.
- Calculate the pH of 0.0150 mol dm−3 HNO3.
- Calculate the pH of 4.00 × 10−3 mol dm−3 Ca(OH)2 at 25 °C.
Mind stretcher 1: Dilution and logarithmsExtension
Question. A strong acid is diluted tenfold. Predict and explain the pH change.
Show Hint
A tenfold dilution changes [H⁺] by one power of ten.
Show Answer
Its [H⁺] becomes one-tenth, so −lg[H⁺] increases by 1.00 pH unit, provided water auto-ionisation is negligible.
Mind stretcher 2: Error analysisExtension
Question. A student obtains pH 1.30 for 0.050 mol dm⁻³ H₂SO₄ by assuming two H⁺ per acid. State why the numerical result needs a stated model.
Show Hint
Distinguish a supplied complete-ionisation model from real second dissociation.
Show Answer
The answer assumes both protons ionise completely. The second dissociation is not necessarily complete, so the calculation is valid only if that simplifying assumption is stated or supplied.