I'm having some trouble with this question. will post my thought process in a bit! For the thermal decomposition of hydrogen sulfide, H2S(g) ↔ 2H2(g) + S2(g), K = 2.2x10-4 at 1,400 K. A sample of gas in which [H2S] = 6.00 M is heated to the decomposition point in a sealed vessel. After equilibrium is reached, what is [H2S]? You can assume that no H2 or S2 was present in the original sample. A. 3.22 M B. 5.75 M C. 4.45 M D. 1.77 M E. 5.10 M
First I balanced the equation: 2H2S(g) ↔ 2H2(g) + S2(g) and use the ICE table, which I would get 2.2*10^-4=(x)*(2x^2)/(6-2x)^2 solving for x, I would get 0.153, plugging it back into the equation is 6-2(0.153)=5.69M but no choices are that concentration. the closest is B 5.75, but I think this question is harder than I think it is.
\[K = 2.2E-4 = \frac{ [H2(g)]^2[S2(g)] }{ [H2S(g)] } = \frac{ [2x]^2[x] }{ [6-2x]^2 } = \frac{ [4x^2][x] }{ [6-2x]^2 } = \frac{ [4x^3] }{ [6-2x]^2 }\] is what i have so far
gosh this equation thingy takes forever to do
I also tried using the free energy side of it. deltaG=-RTln(K) free energy is always 0 at equilibrium so 0=-8.314*1400*ln((x)*(2x^2)/(6-2x)^2) which solving for x would be 1.587, plugging that into the ice table; it would be 6-2(1.587)=2.83M which again is none of the choices
Thanks for staying with me, you can use just the easier way to enter equations if you want to :)
wait
how did you solve for x? I've having a hard time doing that lol
i tried square rooting both sides and got 0.014 = \[\sqrt{x}\]/6-2x
ops i mean, \[0.014 =\frac{ 2x \sqrt{x} }{ 6-2x }\]
ya i was going to say that the equation in the problem wasn't balanced lol
But @premedhelp , x can't be 0.153 b/c if you plug back 0.153 into the equilibrium expression, you don't get the same equilibrium constant of 2.2E-4
thats what I was thinking, but doesnt the constant change when you heat it up to the decomposition point? i think thats what im confused about
and neither can it be 1.587 b/c it doesn't give you 2.2E-4
Oh snaps, yes you're definitely right. The eq constant's value changes with temperature, but we're not told the final temperature so we can't find the new eq constant
my other question is if 6M is even the initial concentration of H2S though
yep, has been bugging me an hour
ya it has to be. it can't be the final eq concentration b/c that would be the answer then lol
Look, i think we have our equilibrium expressions set up correctly. I'm thinking that where we're going wrong is actually solving for x
that's all we have to do, solve for x properly
http://www.wolframalpha.com/input/?i=2.2*10^-4%3D%28x%29*%282x^2%29%2F%286-2x%29^2 here could be our reference, just cant get step by step
no you typed it up wrong
it should be (x)(2x)^2 or (x)(4x^2) or just 4x^3
YAY after we type it in correctly, we'll solve this problem correctly YES!
and viola!, x = 0.122 http://www.wolframalpha.com/input/?i=2.2*10%5E-4%3D%28x%29*%284x%5E2%29%2F%286-2x%29%5E2
and just to check, we can plug x = 0.122 into the equilibrium expression and we DO get 2.2E-4 :)
Now we can solve for the equilibrium concentration of H2S(g), which is represented by 6-2x
which is 5.75M!
so we can substitute our new x of 0.122 into 6-2x and we get 5.756
but i would still like to know how we can solve for x manually
YAY! WE FRIGGING DID IT LOL
high five :)
;)
ya me too :(
stay on for a bit, and ill try to figure it out :)
but damn...that wolf ram alpha tho... lol i've never used that before. That program is cool
haha message me it, i'm going to eat right now :) Good luck
i know right! alrighty, eat up! :)
I need some...."food for thought" haha
haha, you're right! If you want to make a friend, I'll add you on fb?
ya sure
i've sent you my fb link to ur message inbox
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