Calculating pH and [H3O+] after dilution

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The discussion focuses on calculating hydronium ion concentration ([H3O+]) in a buffer solution containing 0.200 mol of acetic acid (HC2H3O2) and 0.200 mol of sodium acetate (NaC2H3O2) in 1.00 L of solution. Using the Henderson-Hasselbalch equation, the pH remains constant at the pKa of acetic acid, confirming that the initial concentration of [H3O+] is equal to the pKa. Upon diluting the solution to 2.00 L, the new [H3O+] concentration remains unchanged, illustrating that buffer pH is largely independent of dilution.

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A solution contains 0.200 mol HC2H3O2, 0.200 mol NaC2H3O2, and enough water to make 1.00 L of solution.
a) Calculate the hydronium ion concentration.
b) Calculate the new hydronium ion concentration after the solution is diluted to 2.00 L

For a), I know the pH is just the same as the pKa of the acetic acid using the Henderson-Hasselbalch equation since log([0.200]/[0.200) = 0, and the hydronium concentration is easy to find next. For b), I think the new concentration is just half of a) since adding more water shouldn't affect anything else other than the volume, correct?

However, if the 0.200 mol HC2H3O2 and 0.200 mol NaC2H3O2 were added to enough water to make 2.00 L of solution instead of being diluted from 1.00 L to 2.00 L later, the pH would be the same as in part a) since log([0.100]/[0.100]) = 0.

I was helping a student with this problem; I can't see an error in my thinking, but I can't figure out how to explain the apparent difference between starting with 1.00 L and diluting to 2.00 L as opposed to starting with 2.00 L.
 
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Buffer pH is - to a large extent - independent of dilution, so answer to b is identical to a. See Henderson-Hasselbalch equation - note that in the ratio of concentrations volume cancels out and you are left with ratio of number of moles of acid and conjugate base.
 

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