Chemistry Lab Report: Gravimetric Analysis of A Metal Carbonate

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Gravimetric Analysis of a Metal Carbonate

Lab Question: ​How do we use gravimetric analysis to determine the identity of a Group 1 metal
CO​3​?
Procedure: ​After preparing a crucible and adding a mystery metal carbonate (M​3​CO​3​) sample to
it, heat all the water out of the sample. Then, precipitate the sample in a solution of CaCl₂ and
distilled water, and decant it through a funnel lined with filter paper. Carefully remove the filter
paper and completely dehydrate the precipitate left behind.
Controls:​ We had to keep the amount of time we were heating our sample constant to ensure that
we were not burning our sample. Burning our sample would have rendered it useless and made it
difficult, if not impossible to proceed with the lab and obtain accurate results.
We had to keep the rate of decantering our precipitate into the funnel constant; if we had filtered
our solution too fast some precipitate would have slipped into our excess solution, and if we did
not catch it our results would not be accurate because we would have lost some of our precipitate
and thus, a portion of our sample.
Conclusion: ​After drying and massing our precipitate we discovered that the molar mass of our
metal carbonate was closest to and most likely sodium carbonate (Na​2​CO​3​).
Discussion of Theory: ​CaCl​2​ and the M​2​CO​3 ​ are both ionic compounds and are soluble in water
by themselves. However, when these ionic compounds interact in this environment of distilled
water, a double replacement reaction occurs. A double replacement reaction is when the two ions
of an ionic compound swap in a chemical reaction, modeled by AB+CD→AD+CB. Carbonates are
only soluble when bonded to group 1 metals or ammonium, so when M​2​CO​3 reacts
​ with CaCl​2​, an
insoluble precipitate, CaCO​3​,​ forms.
​ We can filter and dehydrate the calcium carbonate, then we
can use the mass to calculate the number of moles of our dehydrated CaCO​3​. We can then use this
information to calculate the molar mass of our M​2​CO​3​ and therefore determine its identity. We
know this because we know how many moles of carbonate we have in our CaCO​3​. Then we can do
some basic algebra to determine how many moles of M​2 ​are in our M​2​CO​3​.
Sources of Error: ​The lab directions clearly stated to put the excess piece of filter paper that we
ripped off into the bottom of the funnel. We did not do this and later we discovered why the lab
directions were so specific- the weight of our filter paper was lighter than when we started so our
results were inaccurate- we had 4.42 percent error. Our calculated molar mass for M​2​CO​3​ ended up
being too big and made it difficult to properly identify our metal carbonate.
If some poor misguided chemistry student decided to use rubber tongs on his hot crucible and the
rubber melted into the sample, the rubber might affect the precipitation of the CaCO​3​. This would
have either result in an extremely inaccurate molar mass or render the results entirely useless
because his sample was contaminated.

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