Experiment 11: The Determination of Avogadro's Number
Experiment 11: The Determination of Avogadro's Number
Experiment 11
The mole is the amount of a substance of a system which contains as many elementary entities as there are atoms in 0.012 kilogram of carbon-12; its symbol is "mol." When the mole is used, the elementary entities must be specified and may be atoms, molecules, ions, electrons, other particles, or specified groups of such particles.2 Avogadros number3, NA represents the number of particles in a mole and has been determined by many different experimentalists, notably Jean Perrin (18701942) and Robert Millikan (1868-1953). It was even calculated by Albert Einstein (1879-1955) in his Ph.D. dissertation! The most accurate number to date represents the number of particles in one mole: NA=6.02214199x1023 and is achieved by Xray crystallography data. This Experiment Unlike most units of measure with which we are familiar (like the dozen), a mole of particles cannot be countedits too large! It is determined experimentally by indirect means, in this case, by an electrolysis experiment. To get a very precise value of Avogadros number, we would need some expensive equipment. However, there are several ways that students can get a reasonably accurate value by inexpensive means, including the experiment described in the following pages. Safety Precautions Sulfuric acid is corrosive. In case of contact with skin, rinse with plenty of water and notify your instructor. Wear goggles at all times in the chemistry laboratory.
2
National Institute of Standards and Technology (NIST), 14th General Conference, 1971. http://physics.nist.gov/cuu/Units/mole.html. Accessed 8/27/2006. 3 This number is also referred to as Loschmidts number, L, named after German chemist Josef Loschmidt who published an article in 1865 that led to the determination of the number of molecules/cm3 of a gas.
Name__________________________
Section_______
(Skip this step if your power supply does not have an adjustable voltage)
3. Add about 50 mL of 0.50M sulfuric acid to your beaker and lower the ring clamp if necessary to immerse part of the electrodes in the acid. If you have a multimeter, set the dial to read DC (direct current), 20 or 20/20m for AMPS (not volts). If you have questions, ask your instructor. 4. Check your setup. Briefly turn the power supply on and increase the voltage until you see a reaction occurring inside the beaker. Adjust the voltage so that you have a very gentle stream of bubbles forming. The current should read somewhere between 0.1 and 0.5 amps (the lower the better). Turn the power off as soon as youve set the voltage. If you do not see a reaction, check all of your connections and ask your instructor. Start the experiment; Collect Data 5. Carefully remove the cathode and anode from your setup. Label one anode and the other cathode so you dont get them confused later. Rinse with acetone and when dry, weigh them to the nearest 0.001 g and record these massesmake sure you know which mass goes with each electrode. These are very important data! 6. Obtain a timer or watch to keep track of the length of your electrolysis. 7. Clamp the electrodes as before. Start the timer and the electrolysis at the same time. Record the current (Amps) every minute. If possible, adjust the voltage to keep the current fairly constant. There will be inevitable fluctuations in the current due to changes in the solution and temperature but your results will be better if the current is as constant as possible. 8. Collect data (Amps, every minute) for 5-10 minutes. Do two trials. 9. To stop the run, try to stop the stopwatch at the same time the power supply is switched off. Record the time elapsed, to the nearest second. 8. Carefully remove the anode and cathode. With extreme care, immerse it in 5ml of ethanol. Do not wipe it. Allow it to dry on a paper towel for a couple of minutes. Record the final mass of the anode and cathode. 9. Repeat once more, using new sulfuric acid and electrodes. (Clean your electrodes or use new electrodes if necessary).
Waste Disposal When finished with both trials, put the sulfuric acid into a marked waste container.
Name__________________________
Section_______
Collecting Data
Use this space to record data and observations. Remember, all data should be recorded in permanent ink.
Name__________________________
Section_______
Calculations
For each, provide a calculation for both trials that you performed. Show your work for Trial 1 values. REPORT AN APPROPRIATE NUMBER OF SIGNIFICANT FIGURES!!! Q1) Calculate the average current during your experiment (in amps) and convert it to units of Coulombs per second. (1 Amp = 1 C/s) Trial 1 = ___________ C/s Trial 2 = ___________ C/s
Q2) Calculate the time that elapsed in seconds for each run. Trial 1 = ___________ s Trial 2 = ___________ s
Q3) Use the answers in Q1 and Q2 to find the total charge (in C) that passed through the circuit. Trial 1 = ___________ C Trial 2 = ___________ C Q4) Use Q3 to calculate the number of electrons in each trial of the electrolysis. (One electron has a charge of 1.6022x10-19 C). Trial 1 = ____________electrons Trial 2 = ____________electrons
Q5) The copper atoms in the anode were converted to Cu2+ ions. Thus, there were two electrons generated by each copper atom. Based on the number of electrons generated in each trial (see Q4), calculate the number of copper atoms lost from the anode in each trial. Trial 1 = ___________ copper atoms Trial 2 = ___________ copper atoms
Name__________________________
Section_______
Q6) Based on your mass measurements, how many grams of copper were lost from your anode* during each trial? (*If this data is compromised, you may use cathode data) Trial 1 = ___________ grams of Cu Trial 2 = ___________ grams of Cu
Q7) Based on Q5 and Q6, calculate the number of copper atoms lost from the anode per gram of copper lost from the anode Trial 1 = ___________ Cu atoms/gram Trial 2 = ___________ Cu atoms/gram
Q8) Use Q7 and the molar mass of copper to calculate the number of copper atoms per mole. Trial 1 = ___________ Cu atoms/mole Trial 2 = ___________ Cu atoms/mole
Q9) Take the average of the two trials in Q8. This is your measured value for Avogadros number, NA. REPORT AN APPROPRIATE NUMBER OF SIGNIFICANT FIGURES!!! NA = ___________ particles/mol
Q10) Calculate your percent error, which is the difference between your measured value and the accepted value (6.022x1023) divided by the accepted value, multiplied by 100 and expressed as a positive value.
% error
Name________________________
Section_______
Follow-Up Questions
1) Presumably, you used your anode data in your calculations. Try the calculations with your cathode data. Report your % error for Avogadros number using cathode data.
2) How would the following sources of error affect your results? Would your value of Avogadros number be higher, lower, or the same compared to the accepted value, 6.22x1023? Explain. a) You wiped your cathode at the end of the experiment, then weighed it post-electrolysis, using this mass to calculate Avogadros number.
b) During the course of the electrolysis, the current decreases significantly. You include all these data in your calculation of Avogadros number.
d) You did not allow your anode to dry completely before taking its mass at the end of the electrolysis.
Page 7 of 9
Name________________________
Section_______
3) Which measurement do you think limited your precision in this experiment to only a couple of decimal places? Explain.
4) You should have observed several chemical changes occurring in the electrolysis. a) Note that the color of the solution changes during the electroplating process. What do you think causes this color change, and where does it come from? Be as specific as possible.
b) Give a plausible explanation for the bubbles seen at the cathode during the electrolysis. Describe further tests you could do to confirm or reject your explanation.
Page 8 of 9
Name________________________
Section_______
3. (a) In the electrolysis, which electrode is attached to the (+) terminal? The (-) terminal?
(b) Why are the electrodes placed in sulfuric acid rather than pure water?
(c) How will you ensure that you dont confuse the anode and cathode during the experiment, especially when cleaning and weighing them?
Page 9 of 9