60 ml60ml 0.2(N) H_2SO_4+40 ml0.2(N)H2SO4+40ml 0.4(N) HCl0.4(N)HCl is given. What is the pH of the solution?

1 Answer
Jul 6, 2017

I got "pH" = 0.60pH=0.60. Notice how you can't really ignore the fact that the second proton on "H"_2"SO"_4H2SO4 will dissociate off of a weak acid.

If you assume that sulfuric acid dissociates 100% twice, you would get a total of "0.006 mols" xx 2 = "0.012 mols H"^(+)0.006 mols×2=0.012 mols H+ from "H"_2"SO"_4H2SO4, which would give you a total "H"^(+)H+ concentration of

["H"^(+)] = "0.012 + 0.016 mols H"^(+)/("60 + 40 mL") xx "1000 mL"/"1 L"[H+]=0.012 + 0.016 mols H+60 + 40 mL×1000 mL1 L

~~ "0.28 M"0.28 M

and consequently, an estimated "pH"pH of

"pH" ~~ -log("0.28 M") = 0.55pHlog(0.28 M)=0.55,

which is about 7.7%7.7% error. If your professor is OK with less than 5%5% accuracy error, then 0.550.55 is not quite good enough...


DISCLAIMER: No approximations are made here.

Normality is defined with respect to the "H"^(+)H+ or "OH"^(-)OH the solute dissociates into the solution.

So, a "0.2 N"0.2 N solution of "H"_2"SO"_4H2SO4 is "0.1 M"0.1 M with respect to "HSO"_4^(-)HSO4, for instance, because "H"^(+)H+ is 2:12:1 with "H"_2"SO"_4H2SO4. (The normality definition assumes 100% dissociation of all protons.)

Note that both sulfuric acid and hydrochloric acid are strong acids, which in principle have a 100% dissociation of their first proton.

If we calculate the mols of H^(+)H+, we can divide by the total volume last to find the final concentration.

"H"_2"SO"_4(aq) -> "HSO"_4^(-)(aq) + "H"^(+)(aq)H2SO4(aq)HSO4(aq)+H+(aq)

"mols HSO"_4^(-) = "0.1 M" xx "0.060 L" = color(green)("0.006 mols first H"^(+))mols HSO4=0.1 M×0.060 L=0.006 mols first H+

"HCl"(aq) -> "H"^(+)(aq) + "Cl"^(-)(aq)HCl(aq)H+(aq)+Cl(aq)

"mols H"^(+) = "0.4 M" xx "0.040 L" = color(green)("0.016 mols H"^(+))mols H+=0.4 M×0.040 L=0.016 mols H+

However, the second sulfuric acid proton is another story.

If we keep going without any approximations, we see that sulfuric acid dissociates into the weak acid, "HSO"_4^(-)HSO4, and that would have the following equilibrium:

"HSO"_4^(-)(aq) + "H"_2"O"(l) rightleftharpoons "SO"_4^(2-)(aq) + "H"_3"O"^(+)(aq)HSO4(aq)+H2O(l)SO24(aq)+H3O+(aq)

"I"" ""0.006 mols"" "-" "" "" "" ""0 mols"" "" ""0.006 mols"I 0.006 mols 0 mols 0.006 mols
"C"" "-x" "" "" "-" "" "" "+x" "" "" "" "+xC x +x +x
"E"" "0.006 - x" "-" "" "" "" "x" "" "" "" "0.006 + xE 0.006x x 0.006+x

K_(a2) = 1.2 xx 10^(-2) = ((x)(0.006 + x))/(0.006 - x)Ka2=1.2×102=(x)(0.006+x)0.006x,

a non-negligible dissociation constant.

Solving this via the quadratic formula gives a physically reasonable xx as

x = "0.00337 mols second H"^(+)x=0.00337 mols second H+

This means from "H"_2"SO"_4H2SO4, you place

"0.006 mols first H"^(+) + "0.00337 mols second H"^(+)0.006 mols first H++0.00337 mols second H+

= "0.009 mols H"^(+)=0.009 mols H+ into solution (to three decimal places).

The total mols of "H"^(+)H+ in solution is then:

overbrace("0.00937 mols H"^(+))^("H"_2"SO"_4) + overbrace("0.016 mols H"^(+))^("HCl") = "0.025 mols H"^(+)

And by using the total volume of the solution, we then get the new concentration of "H"^(+) after the solution was mixed and prepared:

"0.02537 mols H"^(+)/("60 + 40 mL") xx "1000 mL"/"1 L"

= "0.2537 M H"^(+) at equilibrium

Therefore, the "pH" is:

color(blue)("pH") = -log["H"^(+)]

= -log("0.2537 M")

= color(blue)(0.60)