Given the following data, how do I find the mols at equilibrium for this reaction?

#"BrCl"(g) rightleftharpoons 1/2"Br"_2(g) + 1/2"Cl"_2(g)#

#DeltaG_f^@ ("Br"_2(g)) = "3.11 kJ/mol"#
#DeltaG_f^@("BrCl"(g)) = -"0.98 kJ/mol"#

#A)# Find the mols of #"BrCl"(g)# at equilibrium if the volume of the container is fixed at #"1.0 L"#.
#B)# Find the mols of #"Br"_2(g)# at equilibrium.
#C)# Find the mols of #"Cl"_2(g)# at equilibrium.

Answer 1
#n_(BrCl(g),eq) = "0.81 mols"# #n_(Br_2(g),eq) = "0.29 mols"# #n_(Cl_2(g),eq) = "0.29 mols"#

DISCLAIMER: LONG ANSWER!

Well, if we assume a rigid container, we can ignore the volume of the vessel and just use #"mols"#. The idea here is then:
#A)#
#DeltaG_(rxn)^@ = sum_P nu_P DeltaG_(f,P)^@ - sum_R nu_R DeltaG_(f,R)^@#,

where:

#=> ul(DeltaG_(rxn)^@) = overbrace((1/2 cdot "3.11 kJ/mol" + 1/2 cdot "0 kJ/mol"))^"Products" - overbrace((1 cdot -"0.98 kJ/mol"))^"Reactants"#
#=# #ul("2.535 kJ/mol")#
Normally, we could calculate #DeltaG_(rxn)# at nonequilibrium conditions with:
#DeltaG_(rxn) = DeltaG_(rxn)^@ + RTlnQ#,
where #RTlnQ# accounts for the shift away from standard conditions and #Q# would be the reaction quotient.
At chemical equilibrium, the reaction has no tendency to move either direction, so #DeltaG = 0# and #Q -= K#. Thus,
#DeltaG_(rxn)^@ = -RTlnK#,
and the equilibrium constant (by dividing by #-RT# and exponentiating both sides) is:
#ulK = "exp"(-DeltaG_(rxn)^@//RT)#
#= e^(-"2.535 kJ/mol"//("0.008314472 kJ/mol"cdot"K" cdot "298.15 K"))#
#= ul0.3597#
At this point, we can now determine the mols present of #"BrCl"(g)# at equilibrium. Construct an ICE table using #"mols"#:
#"BrCl"(g) rightleftharpoons 1/2"Br"_2(g) + 1/2"Cl"_2(g)#
#"I"" "1.40" "" "" "0" "" "" "" "0# #"C"" "-x" "" "+x//2" "" "+x//2# #"E"" "1.40 - x" "x//2" "" "" "x//2#
#K = ((x//2)^cancel(1//2))^cancel(2)/(1.40 - x) = (x//2)/(1.40 - x) = 0.3597#
This #K# is not small, but solving this is not that bad. Eventually we obtain the physical answer as:
#x = |Deltan_(BrCl(g))| = "0.5858 mols"#
#= 2n_(Br_2(g),eq) = 2n_(Cl_2(g),eq)#

And that means...

#color(blue)(n_(BrCl(g),eq)) = 1.40 - 0.5858 = ulcolor(blue)("0.81 mols")#

Everything follows from here. Now the rest is easy.

#B)#

Refer to the ICE table above to realize that:

#color(blue)(n_(Br_2(g),eq)) = x/2 ~~ ulcolor(blue)("0.29 mols")#
#C)#

Refer to the ICE table above to realize that:

#color(blue)(n_(Cl_2(g),eq)) = x/2 ~~ ulcolor(blue)("0.29 mols")#
And as a check, is #K# still correct?
#K = ((0.5858//2)^(1//2))^2/(1.40 - 0.5858) ~~ 0.3597# #color(blue)(sqrt"")#
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Answer 2

I need the specific data related to the reaction, such as initial concentrations, equilibrium concentrations, or equilibrium constant (if provided), to assist you in finding the moles at equilibrium.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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