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Methanol's concentration at equilibrium is $0.001M$.

Before solving for the concentration, try and intuitively imagine what will happen. Since the second experiment is done under the same conditions as the first one (same 100-L vessel, same catalyst), we could estimate that the equilibrium concentration for this reaction will equal the equilibrium concentration of the first experiment.

Let's approach the problem by using the ICE table method (more here: ); for the first experiment, the of the gases are $0.01M$ for $CO$ and $0.02M$ for $H_2$ (because they're placed in a 100-L vessel)

....$CO_((g)) + 2H_(2(g)) rightleftharpoons CH_3OH_((g))$
I:....0.01........0.02.......................0
C....(-x)..........(-2x).....................(+x)
E:...(0.01-x)...(0.02-2x)...............x

Since we know that the equilibrium concentration of $CH_3OH$ is $0.001M$, we can determine the for this reaction, knowing that the equilibrium concentrations of $CO$ and $H_2$ are 0.01 - 0.001 = 0.009 and 0.02 - 2 * (0.001) = 0.018, respectively,

$K_1 = [CH_3OH]/([CO]*[H_2]^2) = (0.001)/(0.009 * 0.018^2) = 343$

Let's set up the second experiment. The starting concentration for $CH_3OH$ will now be $0.01M$.

....$CH_3OH_((g)) rightleftharpoons CO_((g)) + 2H_(2(g))$
I:...0.01M......................0..............0
C.....(-x).......................(+x)...........(+2x)
E...(0.01-x)...................x...............2x

We know that for the reverse reaction, $K_2 = 1/K_1 = 1/343 = 0.003$, which means that we can determine the equilibrium concentrations of all the gases by finding $x$.

$K_2 = 0.003 = (x * (2x)^2)/(0.01-x) = (4x^3)/(0.01-x)$. This equation produces 3 values for $x$, 2 negative, which will be discarded since concentrations cannot be negative, and one positive, $x=0.009$.

Therefore, the concentrations at equilibrium are

$[CH_3OH] = 0.01 - 0.009 = 0.001M$
$[CO] = 0.009M$
$[H_2] = 2 * 0.009 = 0.018M$

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