TBR OChem S8 Q41

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ajumobim

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The explanation says that only base is added to the water and not acid. Can't HCO3- be considered an acid and protonate 3-methylaniline, causing it to go into the aqueous layer (Tube 4)?
 
The explanation says that only base is added to the water and not acid. Can't HCO3- be considered an acid and protonate 3-methylaniline, causing it to go into the aqueous layer (Tube 4)?

HCO3- is weakly acidic (low hydrogen dissociation constant) and will only protonate a molecule that is strongly basic. 3-methylaniline is weakly basic (due to the amino group) and so protonation by HCO3- wouldn't occur.

Comes back to the idea that behavior of a polyprotic molecule that has already "lost" a hydrogen will be at best weakly basic because it is exponentially harder to "pull away" the second or third hydrogen.
 
Totally agree, @AlteredScale ! Also, just wanted to add that HCO3- is significantly more basic than a molecule like HSO4-, even though both are polyprotic acids that have lost one hydrogen already.

I like to think of it like this. HCO3- is the conjugate base of a weak acid, carbonic acid. If we wrote out its dissociation equilibrium, we'd see H2CO3 ---> H+ + HCO3- ----> H+ + CO3 (2-). For HCO3- to act as a base, it would have to lose a second proton. However, H2CO3 itself is already a very weak acid! If we had HCO3- present in an aqueous solution, it would be much more likely to regain its lost proton (re-forming carbonic acid) than to lose another.

HSO4-, on the other hand, is the conjugate base of a strong acid. While it's still unlikely to lose its one remaining proton, sulfuric acid at least completely dissociates in that aqueous solution. So HSO4-, not being prone to regaining that lost proton, has a notably higher Ka than HCO3-.
 
Totally agree, @AlteredScale ! Also, just wanted to add that HCO3- is significantly more basic than a molecule like HSO4-, even though both are polyprotic acids that have lost one hydrogen already.

I like to think of it like this. HCO3- is the conjugate base of a weak acid, carbonic acid. If we wrote out its dissociation equilibrium, we'd see H2CO3 ---> H+ + HCO3- ----> H+ + CO3 (2-). For HCO3- to act as a base, it would have to lose a second proton. However, H2CO3 itself is already a very weak acid! If we had HCO3- present in an aqueous solution, it would be much more likely to regain its lost proton (re-forming carbonic acid) than to lose another.

HSO4-, on the other hand, is the conjugate base of a strong acid. While it's still unlikely to lose its one remaining proton, sulfuric acid at least completely dissociates in that aqueous solution. So HSO4-, not being prone to regaining that lost proton, has a notably higher Ka than HCO3-.

I definitely learned something new (or perhaps a refresher on memories of come) today, thanks!
 
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