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Licemer1 [7]
4 years ago
13

If you mix 95 degrees C and 5 degrees C what temperature would you get?

Chemistry
1 answer:
forsale [732]4 years ago
4 0

Answer:

Between 5^oC and 95^oC

Explanation:

According to the second law of thermodynamics, heat flows from hotter objects toward colder objects.

Having a mixture of two components, one at a higher temperature of 95^oC and the other one at a lower temperature of 5^oC, heat will flow from the first object to the second one.

The temperature of the first object will decrease and the temperature of the second object will increase. Assuming no phase change, the final equilibrium temperature will be reached between 5^oC and 95^oC.

We cannot tell the exact temperature, unless we know the specific heat capacity of each material and their masses. The first object will give off heat given by:

Q_1 = c_1m_1(95^oC - t_f)

The second object will gain this heat by:

Q_2 = c_2m_2(t_f - 5^oC)

Since the heat given off is equal to the heat gained:

c_1m_1(95^oC - t_f) = c_2m_2(t_f - 5^oC)

Let's say that each object is water with a specific heat capacity of:

c_1 = c_2 = 4.184 \frac{J}{g^oC}

The mass of the first object is 10 g, the mass of the second one is 50 g, then:

4.184 \frac{J}{g^oC}\cdot 10 g\cdot (95^oC - t_f) = 4.184 \frac{J}{g^oC}\cdot 50 g\cdot (t_f - 5^oC)

The equation is simplified to:

950 - 10t_f = 50t_f - 250

60t_f = 1200

t_f = 20^oC

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Answer:

C. Ca_3(PO_4)_2  will precipitate out first

the percentage of Ca^{2+}remaining =  12.86%

Explanation:

Given that:

A solution contains:

[Ca^{2+}] = 0.0440 \ M

[Ag^+] = 0.0940 \ M

From the list of options , Let find the dissociation of Ag_3PO_4

Ag_3PO_4 \to Ag^{3+} + PO_4^{3-}

where;

Solubility product constant Ksp of Ag_3PO_4 is 8.89 \times 10^{-17}

Thus;

Ksp = [Ag^+]^3[PO_4^{3-}]

replacing the known values in order to determine the unknown ; we have :

8.89 \times 10 ^{-17}  = (0.0940)^3[PO_4^{3-}]

\dfrac{8.89 \times 10 ^{-17}}{(0.0940)^3}  = [PO_4^{3-}]

[PO_4^{3-}] =\dfrac{8.89 \times 10 ^{-17}}{(0.0940)^3}

[PO_4^{3-}] =1.07 \times 10^{-13}

The dissociation  of Ca_3(PO_4)_2

The solubility product constant of Ca_3(PO_4)_2  is 2.07 \times 10^{-32}

The dissociation of Ca_3(PO_4)_2   is :

Ca_3(PO_4)_2 \to 3Ca^{2+} + 2 PO_{4}^{3-}

Thus;

Ksp = [Ca^{2+}]^3 [PO_4^{3-}]^2

2.07 \times 10^{-33} = (0.0440)^3  [PO_4^{3-}]^2

\dfrac{2.07 \times 10^{-33} }{(0.0440)^3}=   [PO_4^{3-}]^2

[PO_4^{3-}]^2 = \dfrac{2.07 \times 10^{-33} }{(0.0440)^3}

[PO_4^{3-}]^2 = 2.43 \times 10^{-29}

[PO_4^{3-}] = \sqrt{2.43 \times 10^{-29}

[PO_4^{3-}] =4.93 \times 10^{-15}

Thus; the phosphate anion needed for precipitation is smaller i.e 4.93 \times 10^{-15} in Ca_3(PO_4)_2 than  in  Ag_3PO_4  1.07 \times 10^{-13}

Therefore:

Ca_3(PO_4)_2  will precipitate out first

To determine the concentration of [Ca^+] when  the second cation starts to precipitate ; we have :

Ksp = [Ca^{2+}]^3 [PO_4^{3-}]^2

2.07 \times 10^{-33}  = [Ca^{2+}]^3 (1.07 \times 10^{-13})^2

[Ca^{2+}]^3 =  \dfrac{2.07 \times 10^{-33} }{(1.07 \times 10^{-13})^2}

[Ca^{2+}]^3 =1.808 \times 10^{-7}

[Ca^{2+}] =\sqrt[3]{1.808 \times 10^{-7}}

[Ca^{2+}] =0.00566

This implies that when the second  cation starts to precipitate ; the  concentration of [Ca^{2+}] in the solution is  0.00566

Therefore;

the percentage of Ca^{2+}  remaining = concentration remaining/initial concentration × 100%

the percentage of Ca^{2+} remaining = 0.00566/0.0440  × 100%

the percentage of Ca^{2+} remaining = 0.1286 × 100%

the percentage of Ca^{2+}remaining =  12.86%

5 0
4 years ago
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