For the conversion of glucose to G6P, what is #DeltaG_(rxn)^@#?
#"Glucose"(aq) + "Phosphate"(aq) rightleftharpoons "Glucose-6-phosphate"(aq) + "H"_2"O"(l)# , #DeltaG^@ = "13.8 kJ/mol"#
At a certain extent of reaction:
#["Glucose"] = "19.0 mmol/L"#
#["Phosphate"] = "6.90 mmol/L"#
#["Glucose-6-phosphate"] = "1.70 mmol/L"#
#["H"_2"O"] = "55.5 mol/L"#
At a certain extent of reaction:
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The reaction was:
#"Glucose"(aq) + "Phosphate"(aq) rightleftharpoons "Glucose-6-phosphate"(aq) + "H"_2"O"(l)# ,#DeltaG^@ = "13.8 kJ/mol"#
We know that:
#["Glucose"] = "19.0 mmol/L"# #["Phosphate"] = "6.90 mmol/L"# #["Glucose-6-phosphate"] = "1.70 mmol/L"# #["H"_2"O"] = "55.5 mol/L"#
and we know that the NONSTANDARD change in Gibbs' free energy of reaction,
That is related to the reaction quotient
#DeltaG = DeltaG^@ + RTlnQ# where the standard state for
#DeltaG^@# is defined to be at#25^@ "C"# and#"1 bar"# .
Among the concentrations, water is the tricky one here. The standard state of a solid or liquid is its molar density at
At
#"993.3316 g"/"L" xx "1 mol"/"18.015 g" = "55.139 mol/L"#
In the mass action expression, we divide by the standard state units to make
#(["H"_2"O"])/(["H"_2"O"]^@) = "55.5 mol/L"/"55.139 mol/L" = 1.0065# ,which for example, is what we would insert as the current concentration value of water.
It is, as expected, close to
Now, given all these concentrations, we presumably can calculate the reaction quotient of this reaction:
#Q_c = ((("0.00170 mol/L")/("1 mol/L")) cdot ("55.5 mol/L"/"55.139 mol/L"))/((("0.0190 mol/L")/("1 mol/L")) cdot ("0.00690 mol/L"/"1 mol/L"))#
#= 13.05#
Therefore, the change in Gibbs' free energy for this reaction at
#color(blue)(DeltaG_(rxn)) = DeltaG_(rxn)^@ + RTlnQ_c#
#= "13.8 kJ/mol" + (8.314472 xx 10^(-3) "kJ/mol"cdot"K")(37+"273.15 K")ln(13.05)#
#=# #color(blue)"20.4 kJ/mol"#
Knowing that
Did you determine that it shifted left? Since