Experimental Determination of Avogadro
Experimental Determination of Avogadro
Experimental Determination of Avogadro
Avogadro's Number
From Anne Marie Helmenstine, Ph.D.,
Your Guide to Chemistry.
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Electrochemical Method
Avogadro's number isn't a mathematically derived unit. The number of particles in a mole
of a material is determined experimentally. This method uses electrochemistry to make
the determination. You may wish to review the working of electrochemical cells before
attempting this experiment.
Purpose
Introduction
A mole can be defined as the gram formula mass of a substance or the atomic mass of an
element in grams. In this experiment, electron flow (amperage or current) and time are
measured in order to obtain the number of electrons passing through the electrochemical
cell. The number of atoms in a weighed sample is related to electron flow to calculate
Avogadro's number.
In this electrolytic cell both electrodes are copper and the electrolyte is 0.5 M H2SO4.
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During electrolysis, the copper electrode (anode) connected to the positive pin of the
power supply loses mass as the copper atoms are converted to copper ions. The loss of
mass may be visible as pitting of the surface of the metal electrode. Also, the copper ions
pass into the water solution and tint it blue. At the other electrode (cathode), hydrogen
gas is liberated at the surface through the reduction of hydrogen ions in the aqueous
sulfuric acid solution. The reaction is:
2 H+(aq) + 2 electrons -> H2(g)
This experiment is based on the mass loss of the copper anode, but it is also possible to
collect the hydrogen gas that is evolved and use it to calculate Avogadro's number.
Materials
Procedure
Obtain two copper electrodes. Clean the electrode to be used as the anode by immersing
it in 6 M HNO3 in a fume hood for 2-3 seconds. Remove the electrode promptly or the
acid will destroy it. Do not touch the electrode with your fingers. Rinse the electrode with
clean tap water. Next, dip the electrode into a beaker of alcohol. Place the electrode onto
a paper towel. When the electrode is dry, weigh it on an analytical balance to the nearest
0.0001 gram.
The apparatus looks superficially like this diagram of an electrolytic cell except that you
are using two beakers connected by an ammeter rather than having the electrodes
together in a solution. Take beaker with 0.5 M H2SO4 (corrosive!) and place an electrode
in each beaker. Before making any connections be sure the power supply is off and
unplugged (or connect the battery last). The power supply is connected to the ammeter in
series with the electrodes. The positive pole of the power supply is connected to the
anode. The negative pin of the ammeter is connected to the anode (or place the pin in the
solution if you are concerned about the change in mass from an alligator clip scratching
the copper). The cathode is connected to the positive pin of the ammeter. Finally, the
cathode of the electrolytic cell is connected to the negative post of the battery or power
supply. Remember, the mass of the anode will begin to change as soon as you turn the
power on, so have your stopwatch ready!
You need accurate current and time measurements. The amperage should be recorded at
one minute (60 sec) intervals. Be aware that the amperage may vary over the course of
the experiment due to changes in the electrolyte solution, temperature, and position of the
electrodes. The amperage used in the calculation should be an average of all readings.
Allow the current to flow for a minimum of 1020 seconds (17.00 minutes). Measure the
time to the nearest second or fraction of a second. After 1020 seconds (or longer) turn off
the power supply record the last amperage value and the time.
Now you retrieve the anode from the cell, dry it as before by immersing it in alcohol and
allowing it to dry on a paper towel, and weigh it. If you wipe the anode you will remove
copper from the surface and invalidate your work!