1.1 Calculate the concentration of the unknown.
Reveal worked answer
x = (0.455 − 0.018)/0.842 = 0.519 in the concentration unit used for the standards.
Original practice · not an official paper
Six independent scenarios, 18 short tasks. Work first, then reveal the answer and compare your reasoning.
These are original educational exercises, not reproduced or predicted IB examination questions.
0 of 18 tasks reviewed.
A student prepares a set of standards and records an instrument response. A linear fit is y = 0.842x + 0.018 with R² = 0.997. An unknown gives y = 0.455.
x = (0.455 − 0.018)/0.842 = 0.519 in the concentration unit used for the standards.
It indicates that the chosen linear trend explains almost all variation in the calibration data. It does not prove the method is unbiased, chemically valid, or free from systematic error.
That would require extrapolation. The linear relationship has not been experimentally established beyond the calibrated range, so model error can grow.
Useful tools: Calibration curve · Percentage uncertainty · Significant figures
A 25.00 cm³ sample is titrated three times. Concordant titres are 24.62 cm³ and 24.58 cm³. The reacting stoichiometry is 1:1 and the titrant concentration is 0.1000 mol dm⁻³.
(24.62 + 24.58)/2 = 24.60 cm³.
n = CV = 0.1000 × 0.02460 = 2.460 × 10⁻³ mol.
A titre is the difference between two readings. Under the course linear rule, the absolute reading uncertainties add, so the uncertainty associated with the difference is larger.
Useful tools: Titration stoichiometry · Percentage uncertainty
A reaction warms 100.0 g of a water-like solution from 20.0 °C to 27.5 °C. Use c = 4.18 J g⁻¹ K⁻¹. The reaction amount represented is 0.0500 mol.
q = mcΔT = 100.0 × 4.18 × 7.5 = 3135 J = 3.135 kJ.
The solution gains heat, so the reaction loses heat: qreaction is negative and the calculated ΔH is negative.
Heat can be transferred to the surroundings or apparatus rather than being included in the measured solution temperature rise.
Useful tools: Calorimetry · Error & difference
The same visible endpoint is used in four clock-style trials. One trial reaches the endpoint in 40.0 s and another in 20.0 s.
1/40.0 = 0.0250 s⁻¹ and 1/20.0 = 0.0500 s⁻¹.
The same observable endpoint should correspond to the same extent/threshold in each trial, with the comparison otherwise meaningful.
First order with respect to that reactant because the rate proxy changes by the same factor as concentration.
Useful tools: Reaction rate · Rate order (HL)
A gas sample has P = 101.3 kPa, V = 2.40 dm³ and T = 298.15 K. Assume ideal behaviour.
n = PV/RT = (101.3 × 2.40)/(8.314 × 298.15) ≈ 0.0981 mol.
The ideal-gas equation uses absolute temperature; the proportionality between thermal state and T requires the zero of the Kelvin scale.
Real particles have intermolecular interactions and finite molecular volume; either can matter under some conditions.
Useful tools: Ideal gas equation · Moles, mass & particles
A volumetric measurement is reported as 25.00 ± 0.05 cm³ and a second independent measured factor is 0.1000 ± 0.0005 mol dm⁻³.
(0.05/25.00) × 100 = 0.20%.
Add the percentage uncertainties of the multiplied measured quantities.
Premature rounding can accumulate error. Keep guard digits in working and round the final reported value to a justified precision.
Useful tools: Percentage uncertainty · Uncertainty propagation · Significant figures