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Alex777 [14]
2 years ago
5

The burning of 80.3 g of SiH4 at constant pressure gives off 3790 kJ of heat. Calculate △H for this reaction. SiH4(g) + 2O2(g) ⟶

SiO2(s) + 2H2O(l).
A) -1520 kJ/mol rxn.
B) - 47.2 kJ/mol rxn.
C) - 4340 kJ/mol rxn.
D) -2430 kJ/mol rxn.
E) + 4340 kJ/mol rxn.
Chemistry
1 answer:
Trava [24]2 years ago
7 0

Answer  : The value of ΔH for this reaction is, -1516 kJ/mol

Explanation :

First we have to calculate the moles of SiH_4

\text{Moles of }SiH_4=\frac{\text{Mass of }SiH_4}{\text{Molar mass of }SiH_4}

\text{Moles of }SiH_4=\frac{80.3g}{32.12g/mol}

\text{Moles of }SiH_4=2.5mol

Now we have to calculate the ΔH for this reaction.

As, 2.5 mole of SiH_4 react to gives heat = -3790 kJ

So, 1 mole of SiH_4 react to gives heat = -\frac{3790kJ}{2.5mol}

                                                                                = -1516 kJ/mol

Therefore, the value of ΔH for this reaction is, -1516 kJ/mol

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Calculate the equilibrium concentration of c2o42− in a 0.20 m solution of oxalic acid.
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[C2O2−4] =1.5⋅10−4⋅mol⋅dm−3

Explanation:

For the datasheet found at Chemistry Libretext,

Ka1=5.6⋅10−2 and Ka2=1.5⋅10−4 [1]

for the separation of the primary and second nucleon once oxalic corrosive C2H2O4 breaks up in water at 25oC (298⋅K).

Build the RICE table (in moles per l, mol⋅dm−3, or identically M) for the separation of the primary oxalic nucleon. offer the growth access H+(aq) fixation be x⋅mol⋅dm−3.

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By definition,

Ka1=[C2HO−4(aq)][H+(aq)][C2H2O4(aq)]=5.6⋅10−2

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(dispose of the negative arrangement since fixations can faithfully be additional noteworthy or appreciate zero).

Presently build a second RICE table, for the separation of the second oxalic nucleon from the amphoteric C2HO−4(aq) particle. offer the modification access C2O2−4(aq) be +y⋅mol⋅dm−3. None of those species was out there within the underlying arrangement. (Kw is neglectable) therefore the underlying centralization of each C2HO−4 and H+ are going to be appreciate that at the harmony position of the first ionization response.

R C2HO−4(aq)⇌C2O2−4(aq)+H+(aq)

I 8.13⋅10−2 zero eight.13⋅10−2

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E 8.13⋅10−2−y y eight.13⋅10−2+y

It is smart to just accept that

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b. 8.13⋅10−2+y≈8.13⋅10−2 , and

c. The separation of C2HO−4(aq)

Accordingly

Ka2=[C2O2−4(aq)][H+(aq)][C2HO−4(aq)]=1.5⋅10−4≈(8.13⋅10−2 )⋅y8.13⋅10−2

Consequently [C2O2−4(aq)]=y≈Ka2=1.5⋅10−4]⋅mol⋅dm−3

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