kingjewel1 Posted December 29, 2004 Posted December 29, 2004 hi there, i was hopeful someone could clear this up for me. if i have a solution of H2SO4(aq) and i want to calculate its pH would i count the deprotonations of both H+ ions as equal? eg. if the concentration of my solution is 0.3mol dm-3 what is my pH? is it? a) -lg2[0.3]=0.22 or b) -lg[0.3]=0.52 the thing is the 2 proton is obscured by the first so to say. in a way 1:10 concentration. so... would it be... c) -lg[0.33]=0.48? i like the last one but i've seen both the first two before tell us what you think thanks
budullewraagh Posted December 29, 2004 Posted December 29, 2004 well, they both have dissociation constants and the HSO4- is much less apt to dissociate as the first hydronium cation. look up these constants and take it from there
jdurg Posted December 29, 2004 Posted December 29, 2004 The first proton will deprotonate nearly 100%, so when calculating the pH of H2SO4 it is common practice to just use that solitary proton. The amount of dissociation of HSO4- into H+ and SO4(2-) is negligible on the overall pH. However, if you really wanted to get anal-retentive and get the exact pH, you'd have to get the Ka of HSO4- and use the I.C.E. chart while taking into account the concentration of the H+ ions in solution due to the first deprotonation.
kingjewel1 Posted December 29, 2004 Author Posted December 29, 2004 LOL yup my examiners appear to have certain retention so..... the problem is that i've seen all three answers from 3 different sources. i mean you might aswell use the right answer if that's what they're looking for... would c) be good enough though?
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