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leva [86]
3 years ago
11

The useful metal manganese can be extracted from the mineral rhodochrosite by a two-step process. In the first step, manganese(I

I) carbonate and oxygen react to form manganese(IV) oxide and carbon dioxide:
2MnCOA9 + 02(g) 2 MnO2(s) + 2 CO2(g)
In the second step, manganese(IV) oxide and aluminum react to form manganese and aluminum oxidide
3Mn02(6)+4Als)3Mnsl20s)
Suppose the yield of the first step is 66% and the yield of the second step is 97'%. Calculate the mass of manganese(II) carbonate required to make 4.0 kg of manganese.
Be sure your answer has a unit symbol, if needed, and is rounded to the correct number of significant digits.
Chemistry
1 answer:
ale4655 [162]3 years ago
7 0

Answer:

The answer is "6.52 kg and 13.1 kg"

Explanation:

For point a:  

Actual\ yield = 6.52 \ kg\\\\Percent \ yield= 66\%\\\\Percent \ yield = \frac{Actual \ yield}{Theoretical\ yield} \times 100 \%\\\\Theoretical\ yield \ of \ MnO_2 = \frac{Actual \ yield}{Percent \ yield} \times 100\%\\\\=\frac{6.52 \ kg}{66 \%} \times 100\% =9.88 \ kg\\\\

Equation:  

3MnCO_3 +O_2 \longrightarrow 2MnO_2 + 2CO_2\\\\

Calculating the amount of MnCO_3

= 9.88 \ kg \times \frac{1000 \ g}{1 \ kg} \times \frac{1 \ mol \ MnO_2}{86.94 \ g} \times \frac{2 \ Mol \ MnCO_3}{2 \ mol \ MnO_2} \times \frac{114.95\ g}{1 \ mol \ MnCO_3 }\times \frac{1\ kg}{1000\ g}\\\\=  13.1 \ kg

For point b:

Actual\ yield = 4.0 \ kg\\\\Percent\ yield=97.0\%\\\\Percent \ yield = \frac{Actual \ yield}{Theoretical \ yield} \times 100 \% \\\\Theoretical \ yield\  of\  Mn = \frac{Actual \ yield}{Percent \ yield} \times 100\%\\\\

=\frac{4.0 \ kg}{97.0\%} \times 100\% =4.12 \ kg

Equation:  

3MnO_2 +4AL \longrightarrow 3Mn + 2AL_2O_3\\\\

Calculating the amount of MnO_2:  

= 4.12 \ kg \times \frac{1000 \ g}{1 \ kg} \times \frac{1 \ mol \ Mn}{54.94 \ g} \times \frac{3 \ Mol \ MnO_2}{3 \ mol \ Mn} \times \frac{86.94 \ g}{1 \ mol \ MnO_2 }\\\\=  6516 \ g \\\\=6.52 \ kg\\\\

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Answer:

P(C₆H₆) = 0.2961 atm

Explanation:

I found an exercise pretty similar to this, so i'm gonna use the data of this exercise to show you how to do it, and then, replace your data in the procedure so you can have an accurate result:

<em>"At a certain temperature the vapor pressure of pure benzene (C6H6) is measured to be 0.63 atm. Suppose a solution is prepared by mixing 79.2 g of benzene and 115. g of heptane (C7H16) Calculate the partial pressure of benzene vapor above this solution. Round your answer to 2 significant digits. Note for advanced students: you may assume the solution is ideal".</em>

<em />

Now, according to the data, we want partial pressure of benzene, so we need to use Raoul's law which is:

P = Xₐ * P°    (1)

Where:

P: Partial pressure

Xₐ: molar fraction

P°: Vapour pressure

We only have the vapour pressure of benzene in the mixture. We need to determine the molar fraction first. To do this, we need the moles of each compound in the mixture.

To get the moles:   n = m / MM

To get the molar mass of benzene (C₆H₆) and heptane (C₇H₁₆), we need the atomic weights of Carbon and hydrogen, which are 12 g/mol and 1 g/mol:

MM(C₆H₆) = (12*6) + (6*1) = 78 g/mol

MM(C₇H₁₆) = (7*12) + (16*1) = 100 g/mol

Let's determine the moles of each compound:

moles (C₆H₆) = 79.2 / 78 = 1.02 moles

moles (C₇H₁₆) = 115 / 100 = 1.15 moles

moles in solution = 1.02 + 1.15 = 2.17 moles

To get the molar fractions, we use the following expression:

Xₐ = moles(C₆H₆) / moles in solution

Xₐ = 1.02 / 2.17 = 0.47

Finally, the partial pressure is:

P(C₆H₆) = 0.47 * 0.63

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