How does the polarization of the carbonate ion make the thermal decomposition of CaCO3 more likely?

1 Answer
May 5, 2017

I think I see the confusion. You may not be seeing the intramolecular effects. The decomposition reaction is:

"CaCO"_3(s) stackrel(Delta" ")(->) "CaO"(s) + "CO"_2(g)

The effect of interest is the polarization towards the "Ca"^(2+) cation from the "CO"_3^(2-) anion, causing intramolecular bond weakening.

Yes, there is an ion-pairing attraction going on, but that is not going against the ability of the "CaCO"_3 to decompose when you heat the compound (it is a "Ca"^(2+)-"O"^(2-) ion-pair interaction that will later hold the "CaO"(s) formula unit together, anyways). However, what you should also be looking at is how the polarization facilitates decomposition.

Since the calcium cation is highly-positively-charged, and is somewhat small, one might call it a "hard acid" (from Hard-Soft Acid/Base Theory), because it can capably concentrate negative charge density towards itself, and we call that great polarizing ability. We can also say that "Ca"^(2+) is very electropositive.

Thus, it pulls electron density from the "CO"_3^(2-), specifically within the "C"-"O" bond (since the individual dipoles [that all cancel out] within "CO"_3^(2-) lie along the "C"-"O" bond, making it have the highest vector alignment). This unbalances the electron distribution and makes the "C"-"O" bond more ionic in character. That weakens the "C"-"O" bond, and facilitates breaking the bond.

That bond will be broken upon heating in order to perform the decomposition reaction.