Question #97442
In a constant pressure calorimeter, (1.9290x10^2) mL of a 1.00 M metal chloride solution (MCl2(aq)) were added to (1.9290x10^2) mL of a 0.500 M potassium sulfate solution. The total heat capacity of the calorimeter (including all its contents) was 1.75 kJ oC-1. The temperature in the calorimeter rose from 24.50oC to (2.96x10^1) oC. Calculate the enthalpy change (in kJ/mol) for the precipitation reaction: M2+(aq) + SO42-(aq) → MSO4(s).
1
Expert's answer
2019-10-28T08:22:52-0400

Solution.

Assume that the heat capacity of salt solutions is equal to the heat capacity of water. Now let's find a substance in excess (the limiting reagent):

n(MCl2)=0.1929×1=0.1929 moln(MCl2) = 0.1929 \times 1 = 0.1929 \ mol

n(K2SO4)=0.1929×0.5=0.0965 moln(K2SO4) = 0.1929 \times 0.5 = 0.0965 \ mol

K2SO4 is limiting reagent.

According to the reaction equation, the amount of substance sulfate ions is equal to the amount of substance insoluble compound, so n(K2SO4) = n (MSO4).

According to the condition of the problem, the water (solutions) and the calorimeter were in equilibrium, then:

Q(cal)=Q(H2O)Q(cal) = Q(H2O)

Q(cal)=C(cal)ΔtQ(cal) = C(cal) * \Delta t

Q(cal)=1.75×103×(29.624.5)=8.925×103 JQ(cal) = 1.75 \times 10^3 \times (29.6-24.5) = 8.925 \times 10^3 \ J

The amount of heat is equal to the enthalpy of the reaction taken with the inverse sign, so:

ΔH=Q\Delta H = -Q

ΔH(mole)=Qn(MSO4)\Delta H(mole) = \frac{-Q}{n(MSO4)}

ΔH(mole)=8.925×1030.0965=92.49 kJmol\Delta H(mole) = \frac{-8.925 \times 10^3}{0.0965} = -92.49 \ \frac{kJ}{mol}

Answer:

ΔH(mole)=92.49 kJmol\Delta H(mole) = -92.49 \ \frac{kJ}{mol}


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