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Monica [59]
2 years ago
13

Calculate the amount, in moles, of PO43- present at equilibrium when excess Sr3(PO4)2 is added to 750. mL 1.2 M Sr(NO3)2(aq). As

sume no change in volume. For Sr3(PO4)2, Ksp = 1.0×10-31.
Chemistry
1 answer:
Crank2 years ago
7 0

Answer:

1.8 × 10⁻¹⁶ mol  

Explanation:

(a) Calculate the solubility of the Sr₃(PO₄)₂

Let s = the solubility of Sr₃(PO₄)₂.

The equation for the equilibrium is

Sr₃(PO₄)₂(s) ⇌ 3Sr²⁺(aq) + 2PO₄³⁻(aq); Ksp = 1.0 × 10⁻³¹

                         1.2 + 3s          2s

K_{sp} =\text{[Sr$^{2+}$]$^{3}$[PO$_{4}^{3-}$]$^{2}$} = (1.2 + 3s)^{3}\times (2s)^{2} =  1.0 \times 10^{-31}\\\text{Assume } 3s \ll 1.2\\1.2^{3} \times 4s^{2} = 1.0 \times 10^{-31}\\6.91s^{2} = 1.0 \times 10^{-31}\\s^{2} = \dfrac{1.0 \times 10^{-31}}{6.91} = 1.45 \times 10^{-32}\\\\s = \sqrt{ 1.45 \times 10^{-32}} = 1.20 \times 10^{-16} \text{ mol/L}\\

(b) Concentration of PO₄³⁻

[PO₄³⁻] = 2s = 2 × 1.20× 10⁻¹⁶ mol·L⁻¹ = 2.41× 10⁻¹⁶ mol·L⁻¹

(c) Moles of PO₄³⁻

Moles = 0.750 L × 2.41 × 10⁻¹⁶ mol·L⁻¹ = 1.8 × 10⁻¹⁶ mol

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2 years ago
Consider a general reaction A ( aq ) enzyme ⇌ B ( aq ) A(aq)⇌enzymeB(aq) The Δ G ° ′ ΔG°′ of the reaction is − 5.980 kJ ⋅ mol −
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Answer : The value of K_{eq} is, 11.2

The value of \Delta G_{rxn} is -9.04 kJ/mol

Explanation :

The relation between the equilibrium constant and standard Gibbs free energy is:

\Delta G^o=-RT\times \ln K_{eq}

where,

\Delta G^o = standard Gibbs free energy  = -5.980 kJ/mol = -5980 J/mol

R = gas constant = 8.314 J/K.mol

T = temperature = 25^oC=273+25=298K

K_{eq}  = equilibrium constant  = ?

Now put all the given values in the above formula, we get:

\Delta G^o=-RT\times \ln K_{eq}

-5980J/mol=-(8.314J/K.mol)\times (298K)\times \ln K_{eq}

K_{eq}=11.2

Thus, the value of K_{eq} is, 11.2

Now we have to calculate the \Delta G_{rxn}.

The formula used for \Delta G_{rxn} is:

The given reaction is:

A(aq)\rightleftharpoons B(aq)

\Delta G_{rxn}=\Delta G^o+RT\ln Q

\Delta G_{rxn}=\Delta G^o+RT\ln \frac{[B]}{[A]}    ............(1)

where,

\Delta G_{rxn} = Gibbs free energy for the reaction  = ?

\Delta G_^o =  standard Gibbs free energy  = -30.5 kJ/mol

R = gas constant = 8.314\times 10^{-3}kJ/mole.K

T = temperature = 37.0^oC=273+37.0=310K

Q = reaction quotient

[A] = concentration of A = 1.8 M

[B] = concentration of B = 0.55 M

Now put all the given values in the above formula 1, we get:

\Delta G_{rxn}=(-5980J/mol)+[(8.314J/mole.K)\times (310K)\times \ln (\frac{0.55}{1.8})

\Delta G_{rxn}=-9035.75J/mol=-9.04kJ/mol

Therefore, the value of \Delta G_{rxn} is -9.04 kJ/mol

3 0
2 years ago
A 0.500 g sample of C7H5N2O6 is burned in a calorimeter containing 600. g of water at 20.0∘C. If the heat capacity of the bomb c
Nata [24]

Answer:

22.7

Explanation:

First, find the energy released by the mass of the sample. The heat of combustion is the heat per mole of the fuel:

ΔHC=qrxnn

We can rearrange the equation to solve for qrxn, remembering to convert the mass of sample into moles:

qrxn=ΔHrxn×n=−3374 kJ/mol×(0.500 g×1 mol213.125 g)=−7.916 kJ=−7916 J

The heat released by the reaction must be equal to the sum of the heat absorbed by the water and the calorimeter itself:

qrxn=−(qwater+qbomb)

The heat absorbed by the water can be calculated using the specific heat of water:

qwater=mcΔT

The heat absorbed by the calorimeter can be calculated from the heat capacity of the calorimeter:

qbomb=CΔT

Combine both equations into the first equation and substitute the known values, with ΔT=Tfinal−20.0∘C:

−7916 J=−[(4.184 Jg ∘C)(600. g)(Tfinal–20.0∘C)+(420. J∘C)(Tfinal–20.0∘C)]

Distribute the terms of each multiplication and simplify:

−7916 J=−[(2510.4 J∘C×Tfinal)–(2510.4 J∘C×20.0∘C)+(420. J∘C×Tfinal)–(420. J∘C×20.0∘C)]=−[(2510.4 J∘C×Tfinal)–50208 J+(420. J∘C×Tfinal)–8400 J]

Add the like terms and simplify:

−7916 J=−2930.4 J∘C×Tfinal+58608 J

Finally, solve for Tfinal:

−66524 J=−2930.4 J∘C×Tfinal

Tfinal=22.701∘C

The answer should have three significant figures, so round to 22.7∘C.

8 0
2 years ago
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