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This IB Chemistry Data Booklet quick reference helps students find and apply the most common constants, units, equations, and tables used in Diploma Programme chemistry. It is designed for Grade 11-12 review, homework, lab calculations, and exam preparation. The goal is to reduce time spent searching and improve accuracy when choosing formulas and units.

Key Facts

  • The gas equation is pV=nRTpV = nRT, where R=8.31 J mol1 K1R = 8.31\ \mathrm{J\ mol^{-1}\ K^{-1}} when pressure is in Pa\mathrm{Pa}, volume is in m3\mathrm{m^3}, and temperature is in K\mathrm{K}.
  • Temperature must be converted using T(K)=T(C)+273.15T\left(\mathrm{K}\right) = T\left({}^{\circ}\mathrm{C}\right) + 273.15 before it is used in gas law or thermodynamic calculations.
  • Specific heat calculations use q=mcΔTq = mc\Delta T, where qq is energy transferred, mm is mass, cc is specific heat capacity, and ΔT\Delta T is the temperature change.
  • Standard enthalpy change can be estimated from bond enthalpies using ΔH=Ebonds brokenEbonds formed\Delta H = \sum E_{\mathrm{bonds\ broken}} - \sum E_{\mathrm{bonds\ formed}}.
  • For a reaction aA+bBcC+dDaA + bB \rightleftharpoons cC + dD, the equilibrium expression is Kc=[C]c[D]d[A]a[B]bK_c = \frac{[C]^c[D]^d}{[A]^a[B]^b}, excluding pure solids and liquids.
  • The relationship between Gibbs free energy and equilibrium is ΔG=RTlnK\Delta G^{\circ} = -RT\ln K, so a larger KK gives a more negative ΔG\Delta G^{\circ}.
  • The standard cell potential is Ecell=EcathodeEanodeE^{\circ}_{\mathrm{cell}} = E^{\circ}_{\mathrm{cathode}} - E^{\circ}_{\mathrm{anode}}, and a positive EcellE^{\circ}_{\mathrm{cell}} indicates a spontaneous cell under standard conditions.
  • Acid-base calculations use pH=log[H+]\mathrm{pH} = -\log[\mathrm{H^+}], pOH=log[OH]\mathrm{pOH} = -\log[\mathrm{OH^-}], and pH+pOH=14.00\mathrm{pH} + \mathrm{pOH} = 14.00 at 298 K298\ \mathrm{K}.

Vocabulary

Standard conditions
Standard conditions are the reference conditions used for many data values, commonly including 100 kPa100\ \mathrm{kPa} pressure, 298 K298\ \mathrm{K} temperature, and 1.00 mol dm31.00\ \mathrm{mol\ dm^{-3}} solutions.
Enthalpy change
Enthalpy change, ΔH\Delta H, is the heat energy transferred by a reaction at constant pressure.
Equilibrium constant
The equilibrium constant, KcK_c, is the ratio of product concentrations to reactant concentrations at equilibrium, each raised to its stoichiometric coefficient.
Standard electrode potential
Standard electrode potential, EE^{\circ}, is the voltage of a half-cell measured against the standard hydrogen electrode under standard conditions.
pH
pH is a logarithmic measure of hydrogen ion concentration given by pH=log[H+]\mathrm{pH} = -\log[\mathrm{H^+}].
Activation energy
Activation energy, EaE_a, is the minimum energy particles need for a successful reaction collision.

Common Mistakes to Avoid

  • Using Celsius in gas law calculations is wrong because equations such as pV=nRTpV = nRT require absolute temperature in K\mathrm{K}.
  • Mixing units in pV=nRTpV = nRT gives incorrect answers because R=8.31 J mol1 K1R = 8.31\ \mathrm{J\ mol^{-1}\ K^{-1}} matches Pa\mathrm{Pa} and m3\mathrm{m^3}, not kPa\mathrm{kPa} and dm3\mathrm{dm^3} unless units are converted consistently.
  • Including pure solids or liquids in KcK_c expressions is wrong because their concentrations are treated as constant and are not written in the equilibrium expression.
  • Reversing an electrochemical cell calculation is wrong because EcellE^{\circ}_{\mathrm{cell}} must be calculated as EcathodeEanodeE^{\circ}_{\mathrm{cathode}} - E^{\circ}_{\mathrm{anode}}.
  • Forgetting that pH is logarithmic is wrong because a change from pH 3\mathrm{pH}\ 3 to pH 4\mathrm{pH}\ 4 means the hydrogen ion concentration changes by a factor of 1010, not by 11.

Practice Questions

  1. 1 A gas has n=0.250 moln = 0.250\ \mathrm{mol}, T=298 KT = 298\ \mathrm{K}, and V=5.00 dm3V = 5.00\ \mathrm{dm^3}. Calculate the pressure in kPa\mathrm{kPa} using pV=nRTpV = nRT.
  2. 2 A 50.0 g50.0\ \mathrm{g} sample of water warms from 22.0 C22.0\ {}^{\circ}\mathrm{C} to 31.5 C31.5\ {}^{\circ}\mathrm{C}. Calculate qq using q=mcΔTq = mc\Delta T and c=4.18 J g1 K1c = 4.18\ \mathrm{J\ g^{-1}\ K^{-1}}.
  3. 3 For N2(g)+3H2(g)2NH3(g)\mathrm{N_2(g)} + 3\mathrm{H_2(g)} \rightleftharpoons 2\mathrm{NH_3(g)}, write the expression for KcK_c.
  4. 4 Explain why the data booklet gives standard electrode potentials as reduction potentials and how that affects the choice of cathode and anode in a galvanic cell.

Understanding IB Chemistry Data Booklet Quick Reference

A data booklet is most useful when you treat it as a map of quantities, not as a list to memorise blindly. Start every calculation by writing what each value means and its unit. A pressure in kilopascals, a volume in cubic decimetres, and a temperature in degrees Celsius may be sensible measurements, yet they may not fit the version of an equation you plan to use.

Unit conversion is not decoration. It changes the numerical answer.

Kelvin is required in calculations involving particle energy because zero kelvin represents the lowest possible thermal energy on that scale. A temperature difference can be expressed in kelvin or degrees Celsius because the size of one interval is the same.

Thermochemistry questions often test careful thinking about boundaries. The system is the chemicals undergoing change. Everything outside it is the surroundings, such as water in a calorimeter.

If the water warms, it gains energy and the reaction loses energy. These energy changes have equal sizes but opposite signs in an ideal experiment. Real calorimeters lose some energy to the container and air, so experimental values can differ from accepted values.

Bond enthalpy calculations need a different kind of care. They use average values from many compounds, so they provide estimates rather than exact results.

Count every bond in the reactants before the reaction, then count every bond in the products after the reaction. Coefficients in a balanced equation change the total number of bonds.

Equilibrium does not mean a reaction has stopped. Forward and reverse reactions continue at the same rate. The concentrations remain steady because both changes balance over time.

The equilibrium constant describes the position of this balance at one temperature. A very large value means products are favoured, but it does not tell you how quickly equilibrium is reached. Catalysts speed up both directions and do not change the equilibrium constant.

When building an equilibrium expression, use the balanced equation rather than the word equation. The powers come from the coefficients.

Pure solids and pure liquids are left out because their effective concentrations remain constant. This matters in reactions involving precipitates, water, or metal electrodes.

Electrochemistry connects chemical change with electron transfer. Reduction happens at the cathode and oxidation happens at the anode. Electrons travel through the external wire from anode to cathode.

Tables of standard reduction potentials can predict the direction of a cell reaction, but a listed potential is not multiplied when an equation is multiplied. Potential is energy per unit charge, not a total amount of energy. Acid base work needs similar attention to scale.

The pH scale is logarithmic, so a change of one pH unit represents a tenfold change in hydrogen ion concentration. Keep extra digits during logarithm calculations, then round the final answer to match the concentration data. The familiar relationship between pH and pOH applies at a stated temperature, so do not assume the same value automatically when temperature changes.