Acids — OCR A-Level Chemistry
Teaching note checked against the official specification.
Test yourself on Acids with OCR A-Level practice questions.
A week of Premium from your first lesson · Then the free plan continues · No card, no charge
Acids explained
Acids covers 9 specification points, including Acids, bases, alkalis and neutralisation and (a) the formulae of the common acids (HCl,….
Read the full explanation
Open a point below for its explanation and revision guidance.
Acids, bases, alkalis and neutralisation
This section introduces the Brønsted–Lowry model: an acid is a proton donor and a base is a proton acceptor. An alkali is a base that dissolves in water to release hydroxide ions, so all alkalis are bases but not all bases are alkalis. Neutralisation occurs when an acid reacts with a base to form a salt and water, and in terms of ions the hydrogen ions from the acid combine with hydroxide ions to form water. Read the specification statements alongside your textbook and class notes, and check that you can write balanced equations for reactions such as hydrochloric acid with sodium hydroxide, and identify the acid, base and salt in each case. Use the reading to build a clear distinction between the general term base and the more specific term alkali, and to practise writing ionic equations for neutralisation.
(a) the formulae of the common acids (HCl, H₂SO₄, HNO₃ and CH₃COOH) and the common alkalis (NaOH, KOH and NH₃) and explanation that acids release H⁺ ions in aqueous solution and alkalis release OH⁻ ions in aqueous solution
Acids and alkalis are identified by their formulae and by the ions they release in water. Learn the four common acids: hydrochloric acid HCl, sulfuric acid H₂SO₄, nitric acid HNO₃ and ethanoic acid CH₃COOH. Learn the three common alkalis: sodium hydroxide NaOH, potassium hydroxide KOH and ammonia NH₃. In aqueous solution an acid releases H⁺ ions, so HCl gives H⁺ and Cl⁻, and H₂SO₄ gives 2H⁺ and SO₄²⁻. An alkali releases OH⁻ ions in aqueous solution: NaOH gives Na⁺ and OH⁻, KOH gives K⁺ and OH⁻. Ammonia is the exception to watch: NH₃ accepts H⁺ from water to form NH₄⁺ and OH⁻, so the OH⁻ ions appear indirectly. A multiple-choice question may ask which species is released, which formula is an alkali, or which ion is present in excess.
(b) qualitative explanation of strong and weak acids in terms of relative dissociations
A strong acid dissociates almost completely in aqueous solution, so nearly every acid molecule releases its H⁺ ions. Hydrochloric acid is a strong acid: HCl → H⁺ + Cl⁻, and the equilibrium lies far to the right. A weak acid dissociates only partially, so most molecules remain undissociated and only a small fraction release H⁺ ions. Ethanoic acid is a weak acid: CH₃COOH ⇌ CH₃COO⁻ + H⁺, with the equilibrium lying to the left. The qualitative explanation compares the extent of dissociation, not the concentration of the solution. A dilute strong acid can have a lower H⁺ concentration than a concentrated weak acid, so keep the two ideas separate. A multiple-choice question may ask which acid is strong, which equilibrium position applies, or how the relative numbers of ions compare.
(c) neutralisation as the reaction of:
This row is a heading that introduces the sub-statement (i), so read it as the frame for the whole neutralisation idea rather than as a standalone fact. In OCR A Level Chemistry (H432) section 2.1.4 Acids, neutralisation is defined by what reacts: an acid supplies H⁺ ions and a base supplies OH⁻ ions, and those ions combine. The heading tells you the specification defines neutralisation by the reacting species, not by a colour change or a pH value. When you revise, build the ionic equation H⁺ + OH⁻ → H₂O and be ready to apply it to strong and weak acids and to alkalis such as NaOH and NH₃. Treat the sub-statement (i) as the assessed content and use this heading to organise your notes around the ions involved.
(i) H⁺ and OH⁻ to form H₂O
This sub-statement requires you to know that in neutralisation, hydrogen ions from the acid react with hydroxide ions from the base to form water. The ionic equation is H⁺ + OH⁻ → H₂O, and it is the same for any strong acid reacting with any strong alkali because the other ions are spectators. For example, hydrochloric acid and sodium hydroxide give Na⁺ and Cl⁻ as spectator ions, so the ionic equation is H⁺ + OH⁻ → H₂O. A multiple-choice question may ask you to pick the correct ionic equation, identify the spectator ions, or recognise that the reaction is H⁺ donating to OH⁻. Check the charges balance: one 1⁺ ion plus one 1⁻ ion gives a neutral product.
(ii) acids with bases, including carbonates, metal oxides and alkalis (water-soluble bases), to form salts, including full equations
An acid reacts with a base to give a salt and, in most cases, water. A base is a proton acceptor; an alkali is a base that dissolves in water, so all alkalis are bases but not all bases are alkalis. With a metal oxide such as copper(II) oxide, the acid is neutralised: 2HCl(aq) + CuO(s) → CuCl₂(aq) + H₂O(l). With an alkali such as sodium hydroxide, the ionic equation is H⁺(aq) + OH⁻(aq) → H₂O(l). With a carbonate such as calcium carbonate, the acid also releases carbon dioxide: 2HCl(aq) + CaCO₃(s) → CaCl₂(aq) + H₂O(l) + CO₂(g). Full equations must balance in atoms and charge, and the salt formula follows from the ions involved, for example Al³⁺ with SO₄²⁻ gives Al₂(SO₄)₃.
Acid–base titrations
An acid–base titration uses a burette to add a solution of known concentration to a measured volume of the other solution until the reaction is just complete, marked by an indicator colour change or a pH meter. A suitable indicator changes colour close to the equivalence point; phenolphthalein suits a strong acid with a strong base, while methyl orange suits a strong acid with a weak base. The result allows calculation of an unknown concentration: moles = concentration × volume in dm³, and the balanced equation gives the reacting ratio. For example, if 25.0 cm³ of 0.100 mol dm⁻³ NaOH needs 20.0 cm³ of HCl, then moles of NaOH = 0.100 × 0.0250 = 2.50 × 10⁻³ mol, and the 1:1 equation gives the acid concentration as 2.50 × 10⁻³ ÷ 0.0200 = 0.125 mol dm⁻³.
(d) the techniques and procedures used when preparing a standard solution of required concentration and carrying out acid–base titrations
This point requires practical technique, not just description. For a standard solution, weigh the solid accurately, dissolve it in a small volume of distilled water in a beaker, transfer the solution and rinsings through a funnel into a volumetric flask, then add distilled water to the graduation mark and invert to mix. For a titration, rinse and fill the burette with the titrant, pipette a measured volume of the analyte into a conical flask, and add the indicator before you begin. Run titrant in, swirling continuously, and add it dropwise as the end point approaches. Record the volume at the first permanent colour change and repeat for concordant results.
(e) structured and non-structured titration calculations, based on experimental results of familiar and non-familiar acids and bases.
Titration calculations start from the mean titre in cm³, converted to dm³ by dividing by 1000, and the known concentration of the standard solution, giving amount in moles by n = c × V. The balanced equation gives the mole ratio between the two reactants, so the amount of the unknown is found. Dividing by its volume in dm³ gives its concentration; multiplying by its molar mass gives mass concentration if needed. Structured questions lead you through these steps, while non-structured questions require you to choose the route yourself. The method works for familiar acids and bases such as hydrochloric acid and sodium hydroxide and for unfamiliar ones, because only the balanced equation and the data change.
Your focus
- Define acids and bases using the Brønsted–Lowry model.
- Explain the difference between a base and an alkali.
- Write balanced equations, including ionic equations, for neutralisation reactions.
Show all 29 objectives
- Recall the formulae of HCl, H₂SO₄, HNO₃ and CH₃COOH
- Recall the formulae of NaOH, KOH and NH₃
- Explain that acids release H⁺ ions and alkalis release OH⁻ ions in aqueous solution
- Explain qualitatively why a strong acid dissociates almost completely
- Explain qualitatively why a weak acid dissociates only partially
- Compare strong and weak acids in terms of relative dissociation
- Explain that neutralisation is defined by the reaction of H⁺ ions with OH⁻ ions.
- Write the ionic equation H⁺ + OH⁻ → H₂O for a neutralisation reaction.
- Apply the definition to reactions of common acids with alkalis such as sodium hydroxide and ammonia.
- Write the ionic equation H⁺ + OH⁻ → H₂O for a neutralisation reaction.
- Identify spectator ions and explain why they are omitted from the ionic equation.
- Check that charge is balanced in an ionic equation.
- Write balanced full equations for reactions of acids with metal oxides, alkalis and carbonates
- Deduce the formula of a salt from the charges on its ions
- Explain the difference between a base and an alkali
- Write the ionic equation for neutralisation of an acid by an alkali
- Carry out mole calculations using concentration and volume in dm³
- Use a balanced equation to relate moles of acid and base at the equivalence point
- Select a suitable indicator for a given acid–base titration
- Calculate an unknown concentration from titration data
- Describe the procedure for preparing a standard solution of known concentration.
- Describe the procedure for carrying out an acid–base titration.
- Explain the purpose of key steps such as rinsings, indicator addition and dropwise delivery near the end point.
- Carry out a multi-step titration calculation from experimental results
- Apply a mole ratio from a balanced equation to find an unknown amount
- Solve non-structured titration problems involving unfamiliar acids and bases
Acids exam tips
Marking Points
- Identifies HCl, H₂SO₄, HNO₃ and CH₃COOH as the common acids named in the specification
- Identifies NaOH, KOH and NH₃ as the common alkalis named in the specification
- States that acids release H⁺ ions in aqueous solution
- States that alkalis release OH⁻ ions in aqueous solution
- Recognises that NH₃ produces OH⁻ ions in water by accepting H⁺ to form NH₄⁺
- States that a strong acid dissociates almost completely in aqueous solution
- States that a weak acid dissociates only partially in aqueous solution
- Links the position of equilibrium to the extent of dissociation for a named acid
- Distinguishes extent of dissociation from concentration of the solution
- Identifies HCl as strong and CH₃COOH as weak using relative dissociation
- Writes the ionic equation H⁺ + OH⁻ → H₂O for the neutralisation reaction.
- Identifies that the hydrogen ion comes from the acid and the hydroxide ion comes from the base.
- Recognises that spectator ions such as Na⁺ and Cl⁻ are omitted from the ionic equation.
- Checks that charge balances, with one 1⁺ ion and one 1⁻ ion forming a neutral water molecule.
- Balances every full equation in atoms and in charge, adjusting coefficients until both sides agree
- Identifies the salt formed from the metal or ammonium ion of the base and the anion of the acid
- Writes the ionic equation for neutralisation as H⁺(aq) + OH⁻(aq) → H₂O(l)
- Includes carbon dioxide as a product when an acid reacts with a carbonate
- Distinguishes an alkali as a water-soluble base rather than a separate class of substance
- Applies the correct formula of a salt using the charges on the cation and anion, for example Al₂(SO₄)₃
- Converts a volume in cm³ to dm³ by dividing by 1000 before multiplying by concentration
- Calculates moles of the known solution as concentration multiplied by volume in dm³
- Uses the balanced equation to find the mole ratio between acid and base
- Selects an indicator whose colour change lies close to the equivalence point
- Calculates the unknown concentration by dividing moles by the volume in dm³
- Reads a burette to the bottom of the meniscus and records to two decimal places
- Describes weighing the solid accurately and dissolving it in a small volume of distilled water before transfer.
- Transfers the solution and beaker rinsings into a volumetric flask and makes up to the graduation mark before mixing.
- Adds the indicator to the measured analyte in the conical flask before starting the titration.
- Runs titrant from the burette with swirling and adds it dropwise as the end point approaches.
- Records the burette reading at the first permanent colour change and repeats to obtain concordant titres.
- Converts the mean titre from cm³ to dm³ by dividing by 1000 before use
- Calculates the amount of the known solution using n = c × V
- Applies the mole ratio from the balanced equation to find the amount of the unknown
- Divides the amount of the unknown by its volume in dm³ to obtain its concentration
- Multiplies concentration by molar mass to find mass concentration where required
- Selects the correct sequence of steps without prompts in a non-structured calculation
Examiner Tips
- 💡Learn the Brønsted–Lowry definitions of acid and base and apply them to unfamiliar examples.
- 💡Practise writing both full and ionic equations for neutralisation reactions.
- 💡Check that each equation is balanced and includes correct state symbols.
- 💡Use the reading to compare an alkali with a base and note the solubility difference.
- 💡Read the question stem to see whether it asks for the ion released or the formula of the compound
- 💡Check each formula against the specification list before selecting an option
- 💡For ammonia, remember the OH⁻ arises through reaction with water, not by direct release
- 💡Use the words 'almost completely' for strong acids and 'partially' for weak acids
- 💡Refer to the equilibrium position when explaining relative dissociation
- 💡Separate the idea of strength from the idea of concentration in your reasoning
- 💡Link this heading directly to sub-statement (i) and write the ionic equation H⁺ + OH⁻ → H₂O in your notes.
- 💡Practise writing the ionic equation for reactions of hydrochloric, sulfuric and nitric acids with sodium hydroxide and with ammonia.
- 💡Check that you can explain why the spectator ions are left out of the ionic equation.
- 💡Learn the ionic equation H⁺ + OH⁻ → H₂O so you can recognise it quickly in a multiple-choice option.
- 💡Check charge balance on both sides before choosing an answer.
- 💡Eliminate options that include spectator ions when the question asks for the ionic equation.
- 💡Check the state symbols and balance the equation atom by atom before selecting an answer
- 💡Recall that acid plus carbonate always gives salt, water and carbon dioxide
- 💡Use ion charges to build the salt formula, then verify the full equation balances
- 💡Read the question carefully to see whether a full equation or an ionic equation is required
- 💡Always convert volumes to dm³ before using moles = concentration × volume
- 💡Write the balanced equation first so the mole ratio is clear
- 💡Check that the indicator's colour change matches the pH at the equivalence point
- 💡Keep units consistent and give the final concentration in mol dm⁻³
- 💡Learn the standard-solution sequence as an ordered list so no transfer or rinsing step is missed.
- 💡State clearly that the indicator goes into the flask before titration and that titrant is added dropwise near the end point.
- 💡Explain why each step matters, such as rinsings ensuring all solute reaches the flask, to show understanding rather than recall alone.
- 💡Write the balanced equation first so the mole ratio is clear before calculating
- 💡Show each stage of working so method marks can be awarded even if the final value is wrong
- 💡Check the units of every quantity before substituting into n = c × V
- 💡For unfamiliar acids or bases, rely on the balanced equation rather than assumed formulae
Common Mistakes
- Treats alkali and base as identical terms; recognise that an alkali is a soluble base that releases hydroxide ions in water.
- Writes neutralisation as producing only a salt; include water as the other product.
- Omits state symbols or charges in ionic equations; include them to show hydrogen ions and hydroxide ions forming water.
- Assumes all bases dissolve in water; distinguish soluble alkalis from insoluble bases.
- Writes the formula of ethanoic acid as CH₃CO₂H without recognising it as the same acid; accept CH₃COOH as the specification form
- Treats NH₃ as releasing OH⁻ directly rather than accepting H⁺ from water to generate OH⁻
- Confuses the ion released by an acid with the ion released by an alkali; acids release H⁺, alkalis release OH⁻
- Omits the subscript ₂ in H₂SO₄ or the subscript ₃ in NH₃; check each subscript carefully
- Confuses a concentrated acid with a strong acid; concentration describes amount per volume, strength describes extent of dissociation
- Claims a weak acid does not dissociate at all; it dissociates partially, so some ions form
- States that a strong acid has a higher concentration than a weak acid; strength and concentration are independent
- Describes dissociation as complete for ethanoic acid; it is partial, shown by an equilibrium arrow
- Treats the heading as a separate examinable fact; instead, use it to organise the sub-statement about H⁺ and OH⁻ forming water.
- Defines neutralisation only by a pH change or indicator colour; instead, define it by the reaction of H⁺ ions with OH⁻ ions.
- Assumes neutralisation always gives a pH of exactly 7; instead, note that the pH at the end point depends on the acid and base used.
- Writes the full molecular equation when an ionic equation is asked for; instead, cancel the spectator ions and show H⁺ + OH⁻ → H₂O.
- Includes Na⁺ and Cl⁻ in the ionic equation; instead, recognise them as spectator ions and omit them.
- Writes the product as H₂O₂ or another formula; instead, use H₂O, since one H⁺ and one OH⁻ combine to give one water molecule.
- Omits water from the equation for an acid with a metal oxide; include H₂O(l) as a product of neutralisation
- Writes the salt formula without balancing ionic charges, giving an incorrect subscript; derive subscripts from the cation and anion charges
- Treats every base as an alkali; state that an alkali is a base that dissolves in water
- Forgets carbon dioxide when an acid reacts with a carbonate; add CO₂(g) to the products
- Uses the volume in cm³ directly in the moles calculation; divide by 1000 to convert to dm³ first
- Ignores the mole ratio from the balanced equation; apply the coefficients before comparing moles
- Chooses an indicator that changes colour far from the equivalence point; match the indicator to the acid and base strength
- Reads the burette from the top of the meniscus; read the bottom of the meniscus at eye level
- Adds the indicator dropwise near the end point; add the indicator to the analyte before the titration begins.
- Makes the volumetric flask up to the mark before transferring all rinsings; include the beaker rinsings in the flask before making up to the mark.
- Stops at the first flash of colour; record the volume at the first permanent colour change and repeat for concordance.
- Uses the titre in cm³ directly in n = c × V; convert to dm³ first by dividing by 1000
- Inverts the mole ratio from the balanced equation; read the coefficients in the equation to set the ratio correctly
- Uses the total volume of the conical flask mixture instead of the titre volume delivered from the burette
- Rounds intermediate amounts too early; carry extra figures and round only the final answer