Year 12

AQA A level Chemistry Acids and Bases Notes

Acids & Bases

— Chemistry · AS Level (7405) · Brønsted–Lowry, strong/weak, pH titration curves —
★ Exam Tip: pH titration curves were newly added to the syllabus (2022 →) — sir calls them easy marks if you learn the few rules. Sketch questions ask for: start pH, end pH, equivalence point at 25 cm³, pH of equivalence point, and a narrow steep part.

1. Brønsted–Lowry Theory of Acids & Bases

DefinitionsAcid = H+ donor   |   Base = H+ acceptor

Remember: H+ is only a proton — an H atom is 1 proton + 1 electron, so once the electron is gone only the proton is left.

Common mistake: a base is an H+ acceptor — NOT an OH− donor/acceptor. Acid gives H+, base takes H+. That is the whole theory.

Conjugate acid–base pairs

Every acid has its own conjugate base, every base has its own conjugate acid. An acid + a base react to give another acid + base.

HA+H 2O → H3O+ +A− acid 1 base 2 acid 2 base 1 conjugate acid–base pair (1) conjugate acid–base pair (2)
HA gives H⁺ to H₂O → H₃O⁺ + A⁻ : two pairs, linked by one H⁺
  • H2O behaved as a base (gained H⁺ → H3O+); HA behaved as an acid (lost H⁺ → A−).
  • A− is the conjugate base of HA; H3O+ is the conjugate acid of H2O.
  • Why? H3O+ now carries an extra H⁺, so if anyone asks for H⁺ it hands it back → acts as an acid. A− has lost its H⁺ and is negative, so it will accept an H⁺ very happily → acts as a base.
Trick: pairs differ by exactly one H⁺. Acid 1 ↔ base 1 and base 2 ↔ acid 2 — label them 1 and 2 to keep track.
Conjugate pair = acid / base differing by only 1 H⁺

Practice — complete & label (a → f)

a) HClacid 1 + H2Obase 2 → H3O+acid 2 + Cl−base 1
b) HNO3acid 1 + H2Obase 2 → H3O+acid 2 + NO3−base 1
c) CH3COOHacid 1 + OH−base 2 → H2Oacid 2 + CH3COO−base 1
d) CH3COOHacid 1 + NH3base 2 → NH4+acid 2 + CH3COO−base 1
e) HNO3acid 1 + OH−base 2 → H2Oacid 2 + NO3−base 1
f) H2SO4acid 1 + OH−base 2 → H2Oacid 2 + HSO4−base 1
Eq. Conjugate pair (1) Conjugate pair (2)
a HCl / Cl⁻ H₃O⁺ / H₂O
b HNO₃ / NO₃⁻ H₃O⁺ / H₂O
c CH₃COOH / CH₃COO⁻ H₂O / OH⁻
d CH₃COOH / CH₃COO⁻ NH₄⁺ / NH₃
e HNO₃ / NO₃⁻ H₂O / OH⁻
f H₂SO₄ / HSO₄⁻ H₂O / OH⁻
Common mistakes (from class):
• The other product is not always H3O+ — OH− + H⁺ → H2O (−1 + 1 = 0; there is no “H₂O⁺”). Watch the + / − charges.
• H2SO4 loses only one H⁺ → HSO4−. Losing both may still be a real reaction, but it is not the conjugate.
• In (f) students paired the wrong species — pairs are H₂SO₄/HSO₄⁻ and H₂O/OH⁻ (each pair differs by one H⁺).
★ Exam Tip: If the examiner says “write the equation showing how the conjugate forms”, gain/lose exactly ONE H⁺ — never more. (Only for conjugate equations — a full neutralisation can move more.)

2. Strong & Weak Acids and Bases

Strong acid: fully ionises (dissociates fully) in aqueous solution. e.g. nitric acid HNO3, sulfuric acid H2SO4, hydrochloric acid HCl

Weak acid: partially ionises in aqueous solution. e.g. ethanoic acid CH3COOH

Strong acid (HCl, HNO₃, H₂SO₄) Weak acid (CH₃COOH)
pH around 1 around 3 (3–5)
Reaction with metals reacts vigorously — lots of bubbles (effervescence of H₂ gas) does not react vigorously — fewer bubbles
Conductivity good conductor (fully dissociated → many ions) bad conductor (few ions)
Note: Observation when an acid reacts with a metal = effervescence; the gas is H2. The board lists only HNO₃, H₂SO₄ and HCl as strong. In class H₃PO₄ was also called “strong” — it is normally treated as a weak acid, so stick to the three on the board and check with sir/your syllabus.
Weak acids in AS: only carboxylic acids (ethanoic acid). Alcohols are NOT acidic — don't list them (A2 topic).

pH scale

0 7 14 acid: 0 < pH < 7 neutral: 7 alkali/base: 7 < pH < 14 strong acid ≈ 1 weak acid ≈ 3 water NH₃ ≈ 9–10 NaOH ≈ 14
where the usual suspects sit on the scale

Neutral pH (7): water — and salts formed from a strong acid + strong base (NaCl, KCl). Not every salt gives pH 7 — key idea for the titration curves later.

Strong base: sodium hydroxide (NaOH), potassium hydroxide (KOH) (also Ca(OH)₂ and Ba(OH)₂, per sir)    Weak base: aqueous ammonia NH3(aq) (Mg(OH)₂ is weak too)

Sir says: if the exam gives an unfamiliar species, they will tell you whether it is strong or weak.

Learn: NaOH & KOH (Group 1 hydroxides) as the strong bases, and NH₃ as the weak base you must know.

3. pH Titration Curves — Key Terms & Set-up

End point: when the indicator changes colour during titration.

Equivalence point: when an acid and base are mixed together in exactly the equation proportions (e.g. 1 mol acid needs 1 mol alkali → they have completely neutralised each other).

Careful: end point and equivalence point are not the same (the indicator need not change exactly at the equivalence point) — not all salts formed during titration have pH 7 at r.t.p. We simply use the end point to find the equivalence point.
• Titration is complete at the equivalence point.
• DO NOT use the term “neutral point”! pH 7 is neutral only at r.t.p. — at other temperatures/pressures the neutral value changes (A2).
Why 25? Same concentration + 1:1 ratio ⇒ volumes are equal ⇒ 25 cm³ needed. (If the ratio were different, the equivalence volume changes.)

Our set-up: we draw every curve for 1 mol dm⁻³ and 25 cm³ of acid or base already in the conical flask, then titrate it with the corresponding 1 mol dm⁻³ solution from the burette. Acid in flask → run alkali in; alkali in flask → run acid in. (Not necessarily the exact numbers in your exam — the method is the same.)

burette 1 mol dm⁻³ opposite solution conical flask 25 cm³ of 1 mol dm⁻³
flask = what is already there; burette = what is added
① START pH= pH of what isalready in theflask ② END pH= pH of what isadded (it endsin excess) ③ STEEP at 251:1 ratio, sameconc. ⇒ eq. pt.at 25 cm³ ④ eq. pt pH= pH of the salt:stronger one“wins”
four questions to answer before drawing ANY titration curve
General shape (all curves): not much change over most of the run → then one sudden steep jump around 25 cm³ (the pH “changes completely”). The steep part is narrow — a thin, near-vertical bit, never a wide sloping stretch. Draw curves, not straight lines.
Who wins? Stronger acid ⇒ salt is acidic (eq. pH < 7), steep part sits in acidic pHs.   Stronger base ⇒ salt is basic (eq. pH > 7), steep part sits in alkaline pHs.   Equal strength ⇒ salt pH 7.
Flipping the graph: “acid into alkali” and “alkali into acid” give the same curve flipped — only the start and end pH swap. Start at what is in the flask, end at what you added in excess.

4. Strong Acid + Strong Base (HCl + NaOH)

HCl + NaOH → NaCl + H2O

1:1 ratio ⇒ 25 cm³ of one needs 25 cm³ of the other (same concentration). NaCl is a neutral salt ⇒ equivalence point at pH 7.

0 2 4 6 8 10 12 14 pH 25 volume of acid added / cm³ MO ✓ PP ✓ eq. pt pH 7 start 14 end 1
running acid into alkali
0 2 4 6 8 10 12 14 pH 25 volume of alkali added / cm³ MO ✓ PP ✓ eq. pt pH 7 start 1 end 14
running alkali into acid (flipped)
Legend: yellow bands = indicator ranges. MO = methyl orange (3.2–4.3), PP = phenolphthalein (8.3–10). ✓ = colour change falls inside the steep part.
  • Steep part covers both alkaline AND acidic pHs (≈13 → 2): a strong acid and strong base are equally strong — neither “wins”. Bracket on the right of each graph.
  • pH changes only over a narrow domain — the steep part is very thin (not a long sloping stretch).
  • Acid into alkali: starts at 14 (NaOH, strong alkali in the flask) and ends at ~1 (excess HCl, strong acid). Flipped: starts at 1, ends at 14.
  • Equivalence point at 25 cm³, pH 7 — they neutralise each other perfectly, NaCl is neutral.
  • Both methyl orange ✓ and phenolphthalein ✓ change colour inside the steep part.
Common mistake: the x-axis of the flipped graph is volume of alkali added (the board reused “acid added” on some flipped graphs — correct it in your answers).

5. Strong Acid + Weak Base (HCl + NH₃)

HCl + NH3 → NH4Cl

Still 1:1 (25 cm³ ↔ 25 cm³). Can also write NH4+ + Cl−. No water forms (NH₃ has no oxygen) — yet it is an acid–base reaction: acid loses H⁺, base gains H⁺. “Salt + water” from O-level is not always the result!

0 2 4 6 8 10 12 14 pH 25 volume of acid added / cm³ MO ✓ PP ✗ eq. pt pH 5 start 12 end 1
acid into alkali
0 2 4 6 8 10 12 14 pH 25 volume of alkali added / cm³ MO ✓ PP ✗ eq. pt pH 5 start 1 end 8–9
alkali into acid (flipped)
  • Strong acid wins ⇒ salt NH4Cl is slightly acidic ⇒ equivalence point at an acidic pH (~5; anything ~4–6 is fine — not as low as 2).
  • Steep part lies in the acidic pHs (≈ 8 → 2): only a little alkaline range (8–7) but lots of acidic range (7–2).
  • Start/end pH: whichever is in the flask starts it — weak base NH3 ≈ 9–12 (sir used 10 in class, the board shows 12 / 8–9); strong acid = 1.
  • Indicator: methyl orange ✓ (3.2–4.3 is inside the steep part); phenolphthalein ✗ (8.3–10 is above it).
Sir's note: the slight bends at the start of these curves are due to buffer solutions (A2). At AS you need not show that bend — a gentle, nearly straight slope is fine. But the overall graph must still be a smooth curve with a narrow steep part, not ruler-drawn straight segments.
Remember: when the acid is strong, the salt is acidic — don’t try to memorise “NH₄Cl is acidic”. Use the rule: strong acid + weak base → strong acid wins → acidic salt.

6. Strong Base + Weak Acid (NaOH + CH₃COOH)

NaOH + CH3COOH → CH3COONa + H2O
0 2 4 6 8 10 12 14 pH 25 volume of acid added / cm³ MO ✗ PP ✓ eq. pt pH 9 start 14 end 5
acid into alkali
0 2 4 6 8 10 12 14 pH 25 volume of alkali added / cm³ MO ✗ PP ✓ eq. pt pH 9 start 4 end 14
alkali into acid (flipped)
Trick: Strong base + weak acid → strong base wins → salt is basic. Same idea, opposite side — no need to memorise pH of salts!
  • Strong base wins ⇒ salt CH3COONa is slightly alkaline ⇒ equivalence point at pH ≈ 9.
  • Steep part lies in the alkaline pHs (strong base) — as much alkaline range as possible, as little acidic as possible.
  • Acid in flask starts at weak-acid pH (~4); acid added in excess ends at ~4–5 (sir: “3, 4, 5 are good estimates”).
  • Indicator: phenolphthalein ✓ (8.3–10 is inside the steep part); methyl orange ✗.

Other strong bases: Ca(OH)₂, Ba(OH)₂ (Group 2 hydroxides); Mg(OH)₂ is a weak base (studied in Group 2). Any unknown species will be described as strong/weak in the question.

7. Weak Acid + Weak Base (CH₃COOH + NH₃)

CH3COOH + NH3 → CH3COO− + NH4+

A titration we never do — the curves show why it is a very bad titration (never titrate CH₃COOH with ammonia).

0 2 4 6 8 10 12 14 pH 25 volume of acid added / cm³ MO ✗ PP ✗ eq. pt pH 7 start 10 end 5
acid into alkali
0 2 4 6 8 10 12 14 pH 25 volume of alkali added / cm³ MO ✗ PP ✗ eq. pt pH 7 start 5 end 10
alkali into acid (flipped)
No clear steep point ⇒ no suitable indicator (both MO ✗ and PP ✗).
  • Both weak ⇒ neither wins ⇒ salt CH3COONH4 (an ionic compound) is neutral ⇒ equivalence point at pH 7, 25 cm³.
  • The steep part is non-existent — it covers neither the alkaline nor the acidic pHs. Just a very short, gentle bump compared with the other curves.
  • Acid-into-alkali: from ~10 (weak base, NH₃) down to ~4–5 (weak acid). Flipped: ~4–5 up to ~10.

8. Indicators

0 2 4 6 8 10 12 14 methyl orange 3.2–4.3 phenolphthalein 8.3–10.0 redyellow colourlesspink/purple ← acidicalkaline →
colour-change ranges (shaded on the pH axis)

① Methyl orange changes colour between 3.2 – 4.3: below this red, above this yellow.

② Phenolphthalein changes colour between 8.3 – 10.0: below this colourless, above this pink/purple.

③ Universal indicator — colour chart below. We don’t use it for titrations: the colour change is gradual and indistinguishable, so it is hard to notice exactly what pH it is at.

1
2
3
4
5
6
7
8
9
10
11
12
13
14

very acidic ←   slightly acidic  | 7 neutral |  slightly alkaline   → very alkaline

★ Golden rule: Always choose an indicator which changes colour within the steep part.   Use methyl orange for a strong acid (with weak base)  •  use phenolphthalein for a strong base (with weak acid).
Titration Salt Eq. pt pH Steep part in MO PP
strong acid + strong base NaCl (neutral) 7 acidic + alkaline ✓ ✓
strong acid + weak base NH₄Cl (acidic) ~5 acidic ✓ ✗
strong base + weak acid CH₃COONa (basic) ~9 alkaline ✗ ✓
weak acid + weak base CH₃COONH₄ (neutral) 7 none / no clear steep part ✗ ✗
Note: the lecture recording supplied ends before the indicators page, so this section follows the board only. Weak + weak has no suitable indicator — that is exactly why it is a bad titration.

9. Past-paper Questions (from the board)

Past paper (d) · Fig 2.1Structured · 5 marks

25 cm³ of 0.10 mol dm⁻³ HCl(aq) is in a beaker, pH recorded. 50 cm³ of 0.10 mol dm⁻³ NH₃(aq) is added in 5 cm³ portions until all is added. HCl is a strong Brønsted–Lowry acid.

(i) [2] Describe what is meant by a strong Brønsted–Lowry acid.

A strong Brønsted–Lowry acid donates H⁺ and completely ionises in aqueous solution.

(ii) [1] NH₃ is a weak base — write an equation showing its behaviour as a weak B–L base in water.

NH3 + H2O ⇌ NH4+ + OH−

board writes “→”; use ⇌ (weak base, only partial) — H₂O donates H⁺ (acid), NH₃ accepts (base).

(iii) [2] Sketch the pH change as HCl(aq) is titrated with NH₃(aq) (axes: pH 0–14, volume NH₃ added 0–50 cm³).

0 2 4 6 8 10 12 14 pH 25 volume NH₃ added / cm³ eq. pt pH ≈ 5 start ~1 end ~9–10
Fig 2.1 answer: slow rise → steep at 25 cm³ → levels off; equivalence point marked (dashed) at pH ≈ 5
Marks: strong acid + weak base ⇒ equivalence pt at acidic pH (~5) not 7; start at strong-acid pH (~1) in the beaker; end at weak-base pH (~9–10); steep part sits mostly in acidic pHs. Mark and label the equivalence point like the board does.
Past paper (d) · Fig 3.2Structured · 5 marks

The hydrogen halides dissolve in water to form strong Brønsted–Lowry acids. The concentration of a strong acid can be found by titration.

(i) [2] State what is meant by strong Brønsted–Lowry acid.  → same answer as above (“Done”): donates H⁺ & completely ionises in aqueous solution.

(ii) [3] On Fig 3.2 sketch the pH curves when (1) 0.1 mol dm⁻³ NaOH(aq), (2) 0.1 mol dm⁻³ NH₃(aq) is added to 25 cm³ of 0.1 mol dm⁻³ HBr(aq), to excess.

0 2 4 6 8 10 12 14 pH 25 volume of NaOH / cm³ eq. pt pH 7 start ~1 end ~14
NaOH + HBr: strong + strong ⇒ eq. pt pH 7, ends ~13–14
0 2 4 6 8 10 12 14 pH 25 volume of NH₃ / cm³ eq. pt pH ≈ 5 start ~1 end ~11
NH₃ + HBr: strong acid + weak base ⇒ eq. pt pH ≈ 5, ends lower (~10–11)
Compare the two curves: same start (~1) and same 25 cm³ — but the strong-base curve goes through pH 7 and finishes higher (~14); the weak-base curve goes through ~5 and finishes lower (~10–11), with its steep part ending lower. Mark the equivalence point on both, at 25 cm³.

10. Quick Recap — Full Chapter Cheat-Sheet

✓ Brønsted–Lowry
  • Acid = H⁺ (proton) donor; base = H⁺ acceptor (not OH⁻!)
  • Conjugate pair: acid ⇌ base differing by exactly 1 H⁺; every acid has a conjugate base and vice-versa
  • HA + H₂O → H₃O⁺ + A⁻ : acid 1/base 1 = HA/A⁻; base 2/acid 2 = H₂O/H₃O⁺  |  OH⁻ + H⁺ → H₂O; H₂SO₄ → HSO₄⁻ (one H⁺ only)
✓ Strong / weak
  • Strong acid = fully ionises (HCl, HNO₃, H₂SO₄): pH ≈ 1, vigorous with metals (H₂ bubbles), good conductor
  • Weak acid = partially ionises (CH₃COOH): pH ≈ 3, slow with metals, poor conductor
  • Strong bases: NaOH, KOH (Group 1/2 hydroxides); weak base: NH₃(aq)
  • pH: acid 0–7 | neutral 7 | alkali 7–14. Only strong acid + strong base give a neutral salt
✓ Titration curves (1 mol dm⁻³, 25 cm³, 1:1 ⇒ eq. pt at 25 cm³)
  • Start = pH of solution in flask; End = pH of solution added in excess. Flip graph if reversed.
  • End point = indicator colour change; equivalence point = exact equation proportions. Never say “neutral point”.
  • SA + SB: eq. pt pH 7, steep spans alkaline + acidic, MO ✓ PP ✓
  • SA + WB: eq. pt ~5 (acidic salt), steep mostly acidic, use methyl orange
  • SB + WA: eq. pt ~9 (basic salt), steep mostly alkaline, use phenolphthalein
  • WA + WB: eq. pt 7, no clear steep part, no suitable indicator → never done
  • Steep part is narrow; draw curves, not straight lines. Indicator must change colour inside the steep part.
✓ Indicators
  • Methyl orange 3.2–4.3 (red → yellow)  |  Phenolphthalein 8.3–10.0 (colourless → pink/purple)
  • Universal indicator not used (gradual, indistinguishable colour change)