H_2H2 (g) + F_2F2 (g) \rightleftharpoons2HF2HF (g), find final values of [H_2]_(eq)[H2]eq, [F_2]_(eq)[F2]eq, and [HF]_(eq)[HF]eq?

k=1.15xx10^2k=1.15×102
If 3.0003.000 mol of H_2H2, F-2F2 and HFHF are added to a 1.5001.500 L flask...

(find final values)

1 Answer
Jun 26, 2018

["H"_2]_(eq) = ["F"_2]_(eq) = "0.471 M"[H2]eq=[F2]eq=0.471 M
["HF"]_(eq) = "5.06 M"[HF]eq=5.06 M


I assume you have given the equilibrium constant K_cKc (not kk, which is a rate constant). Also, we used K_cKc because you gave concentrations.

The reaction was:

"H"_2(g) + "F"_2(g) rightleftharpoons 2"HF"(g)H2(g)+F2(g)2HF(g)

In a "1.500 L"1.500 L flask, the volume is shared, so the initial concentrations are:

["H"_2]_i = "3.000 mols"/"1.500 L" = "2.000 M"[H2]i=3.000 mols1.500 L=2.000 M

["F"_2]_i = "3.000 mols F"_2/"1.500 L" = "2.000 M"[F2]i=3.000 mols F21.500 L=2.000 M

["HF"]_i = "3.000 mols HF"/"1.500 L" = "2.000 M"[HF]i=3.000 mols HF1.500 L=2.000 M

So, the ICE table uses concentrations to give:

"H"_2(g) " "+" " "F"_2(g) " "rightleftharpoons" " 2"HF"(g)H2(g) + F2(g) 2HF(g)

"I"" "2.000" "" "" "2.000" "" "" "2.000I 2.000 2.000 2.000
"C"" "-x" "" "" "-x" "" "" "+2xC x x +2x
"E"" "2.000-x" "2.000-x" "2.000+2xE 2.000x 2.000x 2.000+2x

...remembering that coefficients go into the change in concentration.

Here we assumed that the reaction goes forward. If you calculate Q_cQc, you would find that here it equals 11:

Q_c = ("2.000 M HF")^2/("2.000 M H"_2 cdot "2.000 M F"_2) = 1Qc=(2.000 M HF)22.000 M H22.000 M F2=1

(Since Q_c < K_cQc<Kc, the reaction wants to shift towards the products, so our assumption is good.)

Therefore, we can set up the K_cKc expression:

1.15 xx 10^2 = (2.000 + 2x)^2/((2.000 - x)(2.000 - x))1.15×102=(2.000+2x)2(2.000x)(2.000x)

This is nice in that it is a perfect square. That is one situation where no approximations need to be made and it is quite solvable without the quadratic formula.

sqrt(1.15 xx 10^2) = 10.72 = (2.000 + 2x)/(2.000 - x)1.15×102=10.72=2.000+2x2.000x

We only take K_c > 0Kc>0 because equilibrium constants can never be negative. Proceed to solve for xx:

10.72(2.000 - x) = 2.000 + 2x10.72(2.000x)=2.000+2x

21.45 - 10.72x = 2.000 + 2x21.4510.72x=2.000+2x

19.45 = 12.72x19.45=12.72x

x = "1.53 M"x=1.53 M

Note that we lost a solution of x = "2.69 M"x=2.69 M, but that's OK because it is nonphysical; 2.000 - x2.000x would have given a negative concentration for the reactants.

Anyways, we now get the equilibrium concentrations to be:

color(blue)(["H"_2]_(eq) = ["F"_2]_(eq) = 2.000 - x = "0.471 M")[H2]eq=[F2]eq=2.000x=0.471 M

color(blue)(["HF"]_(eq) = 2.000 + 2x = "5.06 M")[HF]eq=2.000+2x=5.06 M

And just to check,

K_c = (5.06^2)/((0.471)(0.471)) = 115.41 ~~ 115Kc=5.062(0.471)(0.471)=115.41115 color(blue)(sqrt"")