Core practical 13a: Follow the rate of the iodine propanone reaction using a titrimetric method

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Core practical 13a Teacher sheet reaction Specification links WARNING! The product from the reaction, iodopropanone, is a lachrymator (strongly irritant to the eyes). The reaction mixture should be poured down a fume cupboard sink with plenty of running water immediately once each measurement is complete. Consult CLEAPSS Hazcards 54B, 85A, 95C and 98A. Perform a risk assessment using up-to-date information before this practical is carried out. Sodium thiosulfate releases sulfur dioxide when it reacts. Ensure that the room is well-ventilated. Propanone is an irritant and is highly flammable. Sulfuric acid solution is an irritant. Do not run this practical for more than 12 minutes in total. Procedure 1. Mix 25 cm 3 of 1 mol dm 3 aqueous propanone with 25 cm 3 of 1 mol dm 3 sulfuric acid in a beaker. 2. Start the stop clock the moment you add 50 cm 3 of 0.02 mol dm 3 iodine solution. Shake the beaker to mix well. 3. Using a pipette, withdraw a 10 cm 3 sample of the mixture and transfer it to a conical flask. 4. Stop the reaction by adding a spatula measure of sodium hydrogencarbonate. Note the exact time at which the sodium hydrogencarbonate is added. 5. Titrate the remaining iodine present in the sample with 0.01 mol dm 3 sodium thiosulfate(vi) solution, using starch indicator. Copy the table from the analysis section to record your results. 6. Continue to withdraw 10 cm 3 samples at suitable time intervals (approximately every 3 minutes) and treat them similarly. Always note the exact time at which the sodium hydrogencarbonate is added. Practical techniques 1, 4, 11, 12 CPAC 1a, 2a, 2b, 3a, 4a, 4b Notes on procedure This is a complicated procedure. Depending on the ability of the group, it may be necessary to demonstrate this practical first so that students are clear about what to do. Warn students not to stop the clock when they quench the sample, but just to note the time and leave the clock running.

Core practical 13a Teacher sheet Answers to questions 1. The rate doubles. 2. The rate doubles. 3. The rate remains the same. 4. Rate = k[h + ][CH3COCH3] 5. The would be a curve. To prove that the reaction is first order, you can look at the half-life at various points; the half-life will be constant for a first order reaction. Alternatively, plot a of rate against concentration; for a first order reaction this will be a straight-line. Sample data Time hydrogencarbonate added/min 3:00 6:30 9:00 10:30 12:00 Initial reading/cm 3 39.55 29.50 43.90 28.95 46.65 Final reading/cm 3 23.15 14.20 29.50 14.75 28.95 Titre/cm 3 16.40 15.30 14.40 14.20 13.70 The produced (which is approximately linear) shows that the reaction is zero order with respect to iodine. This document may have been altered from the original 2

Core practical 13a Student sheet Follow the rate of the iodine propanone reaction reaction WARNING! The product from the reaction, iodopropanone, is a lachrymator (strongly irritant to the eyes). The reaction mixture should be poured down a fume cupboard sink with plenty of running water immediately once each measurement is complete. Sodium thiosulfate releases sulfur dioxide when it reacts. Ensure that the room is well-ventilated. Propanone is an irritant and is highly flammable. Sulfuric acid solution is an irritant. Do not run this practical for more than 12 minutes in total. All the maths you need Calculate a rate of change from a showing a linear relationship. Equipment 50 cm 3 of 1.0 mol dm 3 aqueous propanone solution 50 cm 3 of 1.0 mol dm 3 sulfuric acid 50 cm 3 of 0.02 mol dm 3 iodine solution (in 0.2 mol dm 3 potassium iodide solution) 0.01 mol dm 3 sodium thiosulfate(vi) solution 20 cm 3 of 1% starch solution/indicator sodium hydrogencarbonate 100 cm 3 beaker conical flasks 10 cm 3 graduated pipette pipette filler spatula stop clock Procedure 1. Mix 25 cm 3 of 1 mol dm 3 aqueous propanone with 25 cm 3 of 1 mol dm 3 sulfuric acid in a beaker. 2. Start the stop clock the moment you add 50 cm 3 of 0.02 mol dm 3 iodine solution. Shake the beaker to mix well. 3. Using a pipette, withdraw a 10 cm 3 sample of the mixture and transfer it to a conical flask. 4. Stop the reaction by adding a spatula measure of sodium hydrogencarbonate. Note the exact time at which the sodium hydrogencarbonate is added. 5. Titrate the remaining iodine present in the sample with 0.01 mol dm 3 sodium thiosulfate(vi) solution, using starch indicator. Copy the table from the analysis section to record your results. 6. Continue to withdraw 10 cm 3 samples at suitable time intervals (approximately every 3 minutes) and treat them similarly. Always note the exact time at which the sodium hydrogencarbonate is added.

Core practical 13a Student sheet Follow the rate of the iodine propanone reaction Analysis of results Time hydrogencarbonate added/min Initial reading/cm 3 Final reading/cm 3 Titre/cm 3 1. Plot a of titre against time. (The titre is proportional to the concentration of iodine.) 2. Deduce the order of reaction with respect to iodine from the. Learning tips The reaction between propanone and iodine in aqueous solution can be catalysed by an acid: I2(aq) + CH3COCH3(aq) + H + (aq) CH3COCH2I(aq) + 2H + (aq) + I (aq) The influence of the iodine on the reaction rate can be studied if the concentrations of propanone and hydrogen ions effectively remain constant during the reaction. This is achieved by using a large excess of both propanone and sulfuric acid in the starting reaction mixture. Questions Similar experiments show that the reaction is first order with respect to both propanone and to hydrogen ions. Use this information to answer the following questions. 1. What is the effect on the rate if the concentration of the hydrogen ions is doubled? 2. What is the effect on the rate if the concentration of the propanone is doubled? 3. What is the effect on the rate if the concentration of the iodine is doubled? 4. Write the overall rate expression for this reaction. 5. Two students monitored the concentration of propanone as the reaction proceeded and plotted a concentration time from their results. What shape would you expect the to be? How would you use this to prove that the reaction is first order with respect to propanone? This document may have been altered from the original 2

Core practical 13a Technician sheet reaction WARNING! The product from the reaction, iodopropanone, is a lachrymator (strongly irritant to the eyes). The reaction mixture should be poured down a fume cupboard sink with plenty of running water immediately once each measurement is complete. Sodium thiosulfate releases sulfur dioxide when it reacts. Ensure that the room is well-ventilated. Consult CLEAPSS Hazcards 54B, 85A, 95C and 98A. Perform a risk assessment using up-todate information before this practical is carried out. Do not run this practical for more than 12 minutes in total. Equipment per student/group Notes on equipment 50 cm 3 of 1.0 mol dm 3 aqueous propanone solution Propanone is an irritant and highly flammable prepare in a well-ventilated room. 50 cm 3 of 1.0 mol dm 3 sulfuric acid Irritant If made from fresh using concentrated sulfuric acid, remember that concentrated sulfuric acid is corrosive and oxidising. 50 cm 3 of 0.02 mol dm 3 iodine solution (in 0.2 mol dm 3 potassium iodide solution) 0.01 mol dm 3 sodium thiosulfate(vi) solution Low hazard Low hazard 20 cm 3 of 1% starch solution/indicator Prepare the solution in boiling water, on the day of the experiment. sodium hydrogencarbonate 100 cm 3 beaker conical flasks 10 cm 3 graduated pipettes pipette filler spatula stop clock