So--I feel I'm overthinking this but it's really, really getting on my nerves.
Apparently, we're to calculate the solubility product constant of PbI2 by using a lab where we added varying amounts of Pb(NO3)2 and KI and watched for a precipitate. Our group's appeared after 2.0 mL of 0.010M Pb(NO3)2 and 1.0 mL of 0.020M KI, though we did have intervals between trials of 1 ml for Pb(NO3)2 and 0.5 for KI.
Our first questions were simple; net ionic equation for the precipitate formed (Pb2+ (aq) + 2I- (aq) -> PbI2 (s))and the Ksp ([Pb2+][I-]2) but the rest is Greek to me despite my A on this unit's test. I feel I'm doing one thing wrong or misinterpreting the question.
For the next question, I calculated the moles of Pb2+ by converting mL to L, and converting 0.002 L to moles using 0.010 M. I got 2.0 X 10-5. Then, I had to find the concentration of Pb2+ in the whole solution we used (which had a total of 0.01 L after adding water), so I divided moles by liters to get 0.002.
The next question was similar but with KI. I followed the same basic concepts as the above paragraph, but because there was 0.001 L converted to moles using 0.020 M, I got the same number of moles as Pb(NO3)2. The concentration out of 10 mL is again requested, but when I convert the moles, I divide by liters and get the same answer as above; 0.002.
I know that PbI2 has twice the moles of I as that of Pb, so I even tried to divide Pb in half and plug everything in to the Ksp. However, I got [0.010][0.020]2 which is 4 x -9 than the accepted Ksp value. The accepted value is 1.39 x 10 -8.
Where am I going crazy?