Calculations
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
n = m / Mr
n = m / Mr underpins nearly every calculation — get this automatic and the rest follow.
Titration concentration
moles = conc x volume
Convert cm^3 to dm^3, then start from the solution whose concentration and volume are both known.
Reacting masses
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
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
c = moles / volume
Convert mass to moles first, then divide by the solution volume in dm3.
Gas volume at RTP
V = n x 24 at RTP
At room temperature and pressure, each mole occupies 24 dm3 or 24 000 cm3.
Limiting reactant
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
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
broken - formed
Breaking takes energy; making releases it. Keep that order in the subtraction.
Reacting gas volumes
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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