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2.4.3Structure and Function in Living Organisms

Practical: Investigating Diffusion and Osmosis

5 min read 8 parts Lesson 13 of 55 1 quiz

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Section 1 of 8Practical 1: diffusion in agar cubes

Diffusion of acid into agar cubes
diffusion in agar cubes explained
The idea
  • The idea Agar is a clear jelly.
    • When made with sodium hydroxide and phenolphthalein indicator, it is pink, because phenolphthalein is pink in alkaline conditions.
  • When dilute hydrochloric acid diffuses into the jelly it neutralises the alkali, and the pink colour disappears.
    • The time this takes shows how fast the acid has reached the middle.
Variables
  • Variables Independent variable: the size of the cube, which changes the surface area to volume ratio.
  • Dependent variablethe time taken for the cube to turn colourless.
  • Control variablesconcentration and volume of acid, temperature, and the agar batch.
Safety
  • Safety Wear eye protection. Dilute hydrochloric acid and the alkaline agar are irritants.
  • Cut the agar on a white tile and cut away from your body, because the scalpel is sharp.

Section 2 of 8Method: agar cubes

Surface area to volume ratio of cubes
Surface Area : Volume — 3D Step-by-Step Simulation
surface area volume ratios
surface area volume ratio
1
Use a scalpel and ruler to cut cubes of pink agar with sides of 0.5 cm, 1 cm and 2 cm.
2
Calculate the surface area, volume and surface area to volume ratio of each cube.
3
Put the same volume of dilute hydrochloric acid, for example 50 cm3, into a boiling tube for each cube.
4
Use forceps to drop a cube into the acid and start the stopwatch immediately.
5
Stop the stopwatch when the cube has become completely colourless and record the time.
6
Repeat at least three times for every size and calculate a mean.

Section 3 of 8Results and evaluation: diffusion

Cube side (cm)SA : VExpected result
0.512 : 1Fastest to turn colourless
16 : 1Intermediate time
23 : 1Slowest to turn colourless

Section 4 of 8Practical 2: osmosis in potato

Osmosis method using potato cylinders
Osmosis across a partially permeable membrane
Temperature practical — Interactive
Osmosis — Partially Permeable Membrane Simulation
r100-osmosis
Osmosis — Progressive Drawing
Osmosis
osmosis across a membrane diagram
Osmosis potato cylinders method (steps 4-6: weigh and record)
Iodine Test on Potato
Osmosis analysis: percentage change in mass table
osmosis experiment in potato cylinders
Osmosis across a partially permeable membrane
Osmosis across a partially permeable membrane
1
Prepare sucrose solutions of several concentrations from 0 mol/dm3 (distilled water) up to 1 mol/dm3, and pour the same volume of each into a labelled test tube.
2
Use a cork borer to cut potato cylinders, then trim them to the same length.
3
Blot each cylinder dry with paper towel and find its initial mass on a balance.
4
Place one cylinder in each tube and leave for a set time, for example several hours.
5
Remove the cylinders, blot them dry in the same way and find their final mass.
6
Calculate the percentage change in mass: (final mass − initial mass) ÷ initial mass × 100.

Section 5 of 8Interpreting the osmosis results

Water uptake by osmosis
Osmosis across a cell membrane (sucrose can't cross)
Potato in sucrose
Distilled water or dilute solution
  • Distilled water or dilute solution Water moves into the potato cells by osmosis, so the mass increases.
    • The cells become firm, or turgid.
Concentrated solution
  • Concentrated solution Water moves out of the cells, so the mass decreases.
    • The cylinders feel soft, and the cell membranes can pull away from the wall (plasmolysis).
Zero change
  • Zero change Where the line on a graph of percentage change crosses zero, the solution has the same water concentration as the potato cells.
    • There is no net movement.

Section 6 of 8Limitations and improvements

Cell Surface Membrane
Membrane diffusion
Partially Permeable Membrane
Agar cubes
  • Agar cubes Judging the exact moment a cube turns colourless is subjective.
    • Measure instead how far (in mm) the acid has travelled after a fixed time.
  • Cubes are hard to cut accurately, so use a sharp scalpel and a ruler.
Potato cylinders
  • Potato cylinders Different potatoes may have different solute concentrations, so use cylinders from the same potato.
  • Blot with the same amount of pressure each time, otherwise unequal surface water affects the mass.

Section 7 of 8Key terms

Paper-Disc Diffusion Method — Simulation
TermMeaning
DiffusionThe net movement of particles from a region of higher concentration to a region of lower concentration.
OsmosisThe diffusion of water across a partially permeable membrane from a dilute solution to a more concentrated solution.
Percentage change in massThe change in mass divided by the starting mass, multiplied by 100.
TurgidDescribes a plant cell that is swollen and firm because it is full of water.
PlasmolysisWhen a plant cell loses so much water that its membrane pulls away from the cell wall.
Partially permeable membraneA membrane that lets some substances pass through but not others.

Section 8 of 8Exam technique

1
Saying that the large agar cube diffuses 'more slowly'. The rate through the jelly is the same; the larger cube takes longer because the acid must travel further and has less surface area per unit of volume.
2
Comparing the final masses of potato cylinders rather than the percentage change, which allows for different starting masses.
3
Forgetting to blot the potato before weighing, so liquid on the surface adds to the mass.
4
Describing osmosis as the movement of sugar. In these experiments it is water that moves, from dilute to concentrated solution.
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