Lesson Beer-Lambert law lessonWorksheet Beer-Lambert law worksheetLab Beer-Lambert law labTest Beer-Lambert law testQuiz Beer-Lambert law quizQuick answer: Molarity is moles of solute per litre of solution, and dilution follows M₁V₁ = M₂V₂. This AP Chemistry lab on Beer-Lambert law gives the aim, the equipment, the safety points, a step-by-step method, sample results and 8 analysis questions; the answers are on a separate page and the lab sheet is a free printable PDF.
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See the book Many drinks and medicines are coloured by dyes whose amount can be measured by light absorption. In this lab you make standards by dilution, measure their absorbance with a colorimeter and test whether absorbance is proportional to concentration. You then use the calibration line to find the dye concentration in an unknown sample.
Level: AP Chemistry · Curriculum: AP Chem Unit 3
AimTo verify the Beer-Lambert law for a blue food dye and to find the concentration of the dye in a sample of drink.
Equipmentstock dye solution of concentration 1.00 × 10⁻⁵ mol/L five 25.00 mL volumetric flasks 10 mL graduated pipette with filler colorimeter with red filter (about 630 nm) and matched cuvettes distilled water, drink sample, tissue SafetySafety Wear goggles and a lab coat. Food dyes stain skin and clothes. Never pipette by mouth. Clean spills on the floor at once, because they are slippery.
MethodPipette 2.50, 5.00, 10.0, 15.0 and 20.0 mL of stock dye into five 25.00 mL flasks and fill each to the mark with distilled water. Fill a cuvette with distilled water and zero the colorimeter (blank). Rinse a cuvette with a little of standard 1, fill it, wipe the sides and measure the absorbance. Repeat for standards 2 to 5, working from the least to the most concentrated. Measure the absorbance of the drink sample, diluted if it is outside the range. Set-up: five numbered volumetric flasks containing blue dye solutions of increasing depth of colour and a colorimeter with a cuvette and a digital absorbance display std 1 std 2 std 3 std 4 std 5 0.521 colorimeter cuvette five standard solutions in 25 mL flasks Standards and colorimeter. ResultsSample data (1.00 cm cuvette, 630 nm). The drink sample gave A = 0.405.
Standard Stock volume (mL) c (10⁻⁶ mol/L) Absorbance 1 2.50 1.00 0.131 2 5.00 2.00 0.258 3 10.0 4.00 0.521 4 15.0 6.00 0.783 5 20.0 8.00 1.036
Analysis questions
Question 1 Check the concentrations Show that the concentration of standard 3 is 4.00 × 10⁻⁶ mol/L.
Question 2 Why a blank Explain why the colorimeter is zeroed with distilled water.
Question 3 Plot the graph Plot A against c and describe the shape. State whether Beer’s law is obeyed.
Question 4 Gradient Calculate the gradient using standards 1 and 5 and state the molar absorptivity.
Question 5 Concentration of the drink Use the line A = 1.30 × 10⁵ c to find c for the drink sample, A = 0.405.
Question 6 Mass concentration The dye has a molar mass of 792.9 g/mol. Calculate the mass of dye per litre of drink in mg.
Question 7 Choice of wavelength Why was a red filter chosen for a blue dye?
Question 8 Improvements State one source of uncertainty and one way to reduce it.
Define molarity. — Moles of solute per litre of solution, mol/L. Dilution equation? — M₁V₁ = M₂V₂ What is conserved in a dilution? — The amount of solute, in moles. Formula for R_f? — Distance moved by spot / distance moved by solvent front. Beer-Lambert law? — A = εbc Units of ε? — L/(mol·cm) Absorbance from transmittance? — A = −log T Absorbance when T = 10 percent? — 1.000 Why use λ_max? — Greatest sensitivity for the measurement. What does a blank do? — Sets A = 0 for solvent and cuvette. Keep going with Lina
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