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Chemistry

Calculations

AQA · GCSE 8462 & A-level 7405

Calculations are where the reliable marks are — and where a missed unit conversion or mole ratio throws them away. Each page gives the key relationship, then a worked exam question you do on paper and mark against an author-written marking guide based on AQA conventions.

GCSE (AQA 8462)

Moles from mass

Higher

n = m / Mr

n = m / Mr underpins nearly every calculation — get this automatic and the rest follow.

Titration concentration

Higher

moles = conc x volume

Convert cm^3 to dm^3, then start from the solution whose concentration and volume are both known.

Reacting masses

Higher

mass → moles → ratio → mass

Mass doesn't go straight to mass — you cross the 'moles bridge' using the balanced equation.

Percentage yield

actual / theoretical x 100

Actual over theoretical. An apparent yield above 100% means the measured 'product' is not a pure, dry product or the calculation/measurement is wrong.

Atom economy

Mr(product) / Mr(reactants) x 100

It's about the balanced equation, not the experiment — desired product over the reactant mass.

Relative formula mass

Mr = sum of Ar values

One missed subscript changes every later answer, so expand the formula before adding.

Relative atomic mass from isotopes

weighted isotope mean

The abundances are weights: multiply first, add, then divide by the total abundance.

Missing mass by conservation

reactant mass = product mass

In a closed system the totals on both sides must match; identify the missing term before subtracting.

Percentage by mass

Higher

element mass / Mr x 100

Count every atom of the chosen element, then compare its total Ar contribution with the whole Mr.

Concentration in g/dm3

c = mass / volume

This concentration is mass per solution volume, so no moles or Mr are needed.

Concentration in mol/dm3

Higher

c = moles / volume

Convert mass to moles first, then divide by the solution volume in dm3.

Gas volume at RTP

Higher

V = n x 24 at RTP

At room temperature and pressure, each mole occupies 24 dm3 or 24 000 cm3.

Limiting reactant

Higher

smallest n/coefficient limits

The smaller mass is not automatically limiting; compare available moles with the equation ratio.

Mean rate of reaction

rate = amount / time

Rate is a change divided by the time interval, with both quantities carrying units.

Rate from a graph tangent

Higher

rate = tangent gradient

An instantaneous rate is the gradient of a tangent, not the gradient between arbitrary curve points.

Chromatography Rf

Rf = spot / solvent

Both distances start at the pencil baseline, and the solvent front always goes underneath the fraction.

Energy change from bond energies

Higher

broken - formed

Breaking takes energy; making releases it. Keep that order in the subtraction.

Reacting gas volumes

Higher

volumes follow coefficients

At the same temperature and pressure, gas volumes follow the balanced equation's mole ratio.

A-level (AQA 7405)

Equilibrium constant Kc

Kc = [products] / [reactants]

Products over reactants, each raised to its balancing number — and the units come from the powers.

pH of a strong acid

pH = -log10[H+]

For a strong monoprotic acid [H+] equals the acid concentration — then it's just -log.

Enthalpy change from calorimetry

q = m c dT ; dH = -q / n

q = m c dT gives the energy; divide by the moles reacted and flip the sign for exothermic.

The ideal gas equation

pV = nRT

pV = nRT only works in SI units — pascals, cubic metres and kelvin — so convert first.

Empirical and molecular formula

mass → moles → ratio

Percentages become masses out of 100 g; masses become moles; only then can you simplify the ratio.

A-level titration stoichiometry

cV → ratio → c

The aliquot volumes belong to different chemicals; attach each volume to its concentration before using the ratio.

Equilibrium constant Kp

Kp from partial pressures

Only gaseous species appear, and every partial pressure is raised to its equation coefficient.

pH of a weak acid

[H+] = sqrt(Ka[HA])

A weak acid is only partly dissociated, so use Ka before taking the negative logarithm.

Buffer pH

[H+] = Ka[acid]/[salt]

Use the weak-acid equilibrium with the acid and conjugate-base concentrations after any neutralisation.

Kw and alkaline pH

[OH-] = Kw/[H+]

Convert pH to [H+] first, then use Kw to find [OH-].

Born-Haber lattice enthalpy

Hess cycle to lattice enthalpy

Give every cycle arrow its sign; electron affinity is often already negative.

Gibbs free energy and feasibility

dG = dH - TdS

Entropy is commonly in J/K/mol while enthalpy is in kJ/mol; align the units before multiplying by temperature.

Rate equation and rate constant

rate = k[A]m[B]n

Orders come from rate data, not balancing coefficients, and k units follow from the final rate equation.

Activation energy from Arrhenius data

two-temperature Arrhenius

Temperatures must be kelvin and the reciprocal-temperature subtraction order must match the logarithm ratio.

Cell EMF from electrode potentials

Ecell = Epositive - Enegative

Keep both values as reduction potentials: more positive minus more negative.

Reaction enthalpy from mean bond enthalpies

broken - formed

Count bonds in the balanced gaseous equation, then subtract energy released making bonds from energy absorbed breaking them.

Water of crystallisation

hydrate mole ratio

The mass lost is water; the mass left is anhydrous salt. Convert both to moles before finding x.

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