In: Chemistry
Thermodynamics of Dissolution of Substance
Reaction Eqn of borax and HCL
B4O5(OH)4 2-(aq) + 2HCl + 3H2O <_> 4H3BO3 (aq) + 2Cl-
Temp |
TRIAL ONE Molarity of HCL |
Volume Borax 1 | Initial Buret Reading | Final Buret Reading |
TRIAL TWO Molarity of HCL |
Volume Borax 2 | Initial Buret Reading | Final Buret Reading |
(°C) | (M) | (mL) | (mL) | (mL) | (M) | (mL) | (mL) | (mL) |
25 | 0.25 | 5 | 18 | 20.45 | 0.25 | 5 | 21 | 23.5 |
calculate
Moles of HCL | Moles of Borate | Concentration of Borate | Ksp | Average Ksp | ΔG | ΔH | ΔS |
(moles) | (moles) | (M) | (Kj/mol) | (Kj/mol) | (J/mol k) |
** I understand that for ΔH ΔS, you need to plot ln(Ksp) vs 1/T and determine their value from that graph.
Values for enthalpy and entropy of the dissolution of borax in water are 110 kJ/mol and 380 J/mol*K respectively. Do your values agree? Calculate your percent error.
You assumed that H and S are constant over the temperature range studied. Are they?
For trial 1:
moles of HCl = 0.25 mol/L * (20.45-18 / 1000)L =
6.125*10-4 mol
moles of borate = 1 mole ( stoichiometry)
concentration of Borate = [6.125*10-4 mol HCl *(1mol
borate/2 mol HCl)] / (5/1000)L
concentration of Borate = 0.06125 M
Ksp = 4 [Borate ion]3 =
4*[0.06125]3 = 9.1913*10-4
For trial 2:
moles of HCl = 0.25 mol/L * (23.5-21 / 1000) = 6.25*10-4
mol
conc of borate = [6.25*10-4 mol HCl *(1mol borate/2 mol
HCl)] / (5/1000)L ] = 0.0625M
Ksp = 4 [0.0625]3 =
9.7656*10-4
Average Ksp = (9.1913+9.7656 / 2) *10-4 =
9.4785*10-4
ln Ksp = (-ΔH/R) *1/T + (ΔS/R)
plot lnKsp Vs 1/T and find slope and y-intercept of that
line ( R=8.314 kJ/mol)
slope = -ΔH/R ; intercept = ΔS/R
percent error in enthalpy= [ | exp value - 110| / exp value ]
*100
similarly you can find percent error for entropy as well
Over the temperature range the values are not constant, they keep
changing over a negligible range
almost.
[To reduce the complexity and to find a solution such assumptions
are made]