This practice question stumped me. What does it mean by calculating delta H for the "base", and how do you solve the question?
When 510mL of a 0.45M Sr(OH)2 solution is mixed with 730mL of a 0.6M H3PO4 solution, the resulting 280g iron calorimeter had an associated temperature increase of 7.5 degrees C. Calculate change in enthalpy (delta H) of the reaction for the base. Assume the solution has a specific heat of 4.18J/gC.
The reaction is as follows: 3Sr(OH)2 + 2H3PO4 --> Sr3(PO4)2 + 6H2O
V = 510 ml
M = 0.45 Sr(OH)2
V2 = 730 ml
M = 0.6M H3PO4
m = 280g of Iron
dT = 7.5ªC
a) Hrxn for the base
Cp = 4.18
Well...
this is a set of echange of heat
Qwin = the iron calorimeter
Qlost = the solution
Qwin = -Qlost
Qwin = m*Cp*dT (all these data is for Iron)
Qwin = 280*0.450*(7.5) = 945 J were transferred
assume no lost to the media
Therefore
Q reaction = Hrxn = 945
But this must be stated per unit mol of base
3Sr(OH)2 + 2H3PO4 --> Sr3(PO4)2 + 6H2O
calculate moles of base that actually reacted
mol base = M*V = 0.45*0.51 = 0.2295 mol of Base
mol of acid = M*V = 0.6*0.73 = 0.438 mol of acid
there is an excess of acid
3 mol of base are needed to neutralize 2 mol of acid
therefore, we are sure that the base is limiting reactant (and probably why they asked you to do this as a basis)
therefore
Hrxn = 945J per 0.2295 mol o Base
Hrxn = 945/0.2295 = 4117.6 J/mol base
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