The value of Kp for the following reaction at 627oC is 6.55. SO2(g) + 1/2O2(g) <---> SO3(g) What is Kc at this temperature?
1 Answer
In the actual answer, we used
#K_c = K_P cdot (1/(RT))^(-1//2) = "56.3 M"^(-1//2)#
where
Below we derive a specific version of the following equation...
#barul|stackrel(" ")(" "K_P = K_c(RT)^(Deltan_"gas")," " Deltan_"gas" = sum_P n_(P) - sum_R n_(R)" ")|# with
#P# being products and#R# being reactants.
Now you don't have to derive this equation for an exam per se... but you do have to know how it works.
Well, we know that for
#1/2"O"_2(g) + "SO"_2(g) -> "SO"_3(g)#
we have that
#K_P = (P_(SO_3))/(P_(SO_2)P_(O_2)^(1//2))# ,
and that
#K_c = ([SO_3])/([SO_2][O_2]^(1//2))# where
#[" "]_i# are molar concentrations in#"mol/L"# and the#P_i# are partial pressures in#"atm"# .
Since these are gases, which are said to (pretty much) fully occupy the container space, we could rewrite this as:
#K_c = (n_[SO_3]//V)/((n_[SO_2]//V)(n_[O_2]//V)^(1//2))# where
#V# is the volume of the container and#n# is the mols of gas.
Assuming these are ideal gases,
#PV = nRT => n/V = P/(RT)# ,where
#R = "0.082057 L"cdot"atm/mol"cdot"K"# .
Therefore,
#K_c = (P_(SO_3)//RT)/((P_[SO_2]//RT)(P_[O_2]//RT)^(1//2))#
#= (P_(SO_3))/(P_[SO_2]P_[O_2]^(1//2)) cdot (1/(RT))^(1 - (1 + 1/2))#
#= (P_(SO_3))/(P_[SO_2]P_[O_2]^(1//2)) cdot (1/(RT))^(-1//2)#
But the first half of
#K_c = K_P (1/(RT))^(-1//2)#
Here the
Since we are at nonstandard temperature,
#K_P = 6.55 (cancel"atm")/(cancel"atm" cdot "atm"^(1//2)) = "6.55 atm"^(-1//2)#
As a result,
#color(blue)(K_c) = K_P (1/(RT))^(-1//2) = K_P (RT)^(1//2)#
#= 6.55 cancel("atm"^(-1//2)) cdot ("0.082057 L"cdotcancel"atm""/mol"cdotcancel"K" cdot (627+273.15 cancel"K"))^(+1//2)#
#= color(blue)("56.3 L"^(1//2)cdot"mol"^(-1//2) = "56.3 M"^(-1//2))#