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jasenka [17]
3 years ago
13

Given these reactions, where X represents a generic metal or metalloid 1 ) H 2 ( g ) + 1 2 O 2 ( g ) ⟶ H 2 O ( g ) Δ H 1 = − 241

.8 kJ 2 ) X ( s ) + 2 Cl 2 ( g ) ⟶ XCl 4 ( s ) Δ H 2 = + 361.7 kJ 3 ) 1 2 H 2 ( g ) + 1 2 Cl 2 ( g ) ⟶ HCl ( g ) Δ H 3 = − 92.3 kJ 4 ) X ( s ) + O 2 ( g ) ⟶ XO 2 ( s ) Δ H 4 = − 607.9 kJ 5 ) H 2 O ( g ) ⟶ H 2 O ( l ) Δ H 5 = − 44.0 kJ what is the enthalpy, Δ H , for this reaction? XCl 4 ( s ) + 2 H 2 O ( l ) ⟶ XO 2 ( s ) + 4 HCl ( g )
Chemistry
1 answer:
Mazyrski [523]3 years ago
6 0

Answer:

-767,2kJ

Explanation:

It is possible to sum enthalpies of half-reactions to obtain the enthalpy of a global reaction using Hess's law. For the reactions:

1) H₂(g) + ¹/₂O₂(g) ⟶ H₂O(g) ΔH₁= −241.8 kJ

2) X(s) + 2Cl₂(g) ⟶ XCl₄(s) ΔH₂= +361.7 kJ

3) ¹/₂H₂(g) + ¹/₂Cl₂(g) ⟶ HCl (g) ΔH₃= −92.3 kJ

4) X(s) + O₂(g) ⟶ XO₂(s) ΔH₄= − 607.9 kJ

5) H₂O(g) ⟶ H₂O(l) ΔH₅= − 44.0 kJ

The sum of (4) - (2) produce:

6) XCl₄(s) + O₂(g) ⟶ XO₂(s) + 2Cl₂(g) ΔH₆ = ΔH₄ - ΔH₂ = -969,6 kJ

(6) + 4×(3):

7) XCl₄(s) + 2H₂(g) + O₂(g) ⟶ XO₂(s) + 4HCl(g) ΔH₇ = ΔH₆ + 4ΔH₃= -1338,8 kJ

(7) - 2×(1):

8) XCl₄(s) + 2H₂O(g) ⟶ XO₂(s) + 4HCl(g) ΔH₈ = ΔH₇ - 2ΔH₁= -855,2kJ

(8) - 2×(5):

9) XCl₄(s) + 2H₂O(l) ⟶ XO₂(s) + 4HCl(g) ΔH₉ = ΔH₈ - 2ΔH₅= <em>-767,2kJ</em>

I hope it helps!

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5 0
2 years ago
If you have access to stock solutions of 1.00 M H3PO4, 1.00 M of HCl, and 1.00 M NaOH solution, (and distilled water of course),
garri49 [273]

Answer:

0.10L of 1.00M of H₃PO₄ and 0.1613L of 1.00M NaOH

Explanation:

The pKa's of phosphoric acid are:

H₃PO₄/H₂PO₄⁻ = 2.1

H₂PO₄⁻/HPO₄²⁻ = 7.2

HPO₄²⁻/PO₄³⁻ = 12.0

To make a buffer with pH 9.40 we need to convert all H₃PO₄ to H₂PO₄⁻ and an amount of H₂PO₄⁻ to HPO₄²⁻

To have a 50mM solution of phosphoures we need:

2L * (0.050mol / L) = 0.10 moles of H₃PO₄

0.10 mol * (1L / mol) = 0.10L of 1.00M of H3PO4

To convert the H₃PO₄ to H₂PO₄⁻ and to HPO₄²⁻ must be added NaOH, thus:

H₃PO₄ + NaOH → H₂PO₄⁻ + H₂O + Na⁺

H₂PO₄⁻ + NaOH → HPO₄²⁻ + H₂O + Na⁺

Using H-H equation we can find the amount of NaOH added:

pH = pKa + log [A⁻] / [HA] <em>(1)</em>

<em>Where [A-] is conjugate base, HPO₄²⁻ and [HA] is weak acid, H₂PO₄⁻</em>

<em>pH = 7.40</em>

<em>pKa = 7.20</em>

[A-] + [HA] = 0.10moles <em>(2)</em>

Replacing (2) in (1):

7.40 = 7.20 + log 0.10mol - [HA] / [HA]

0.2 = log 0.10mol - [HA] / [HA]

1.5849 = 0.10mol - [HA] / [HA]

1.5849 [HA] = 0.10mol - [HA]

2.5849[HA] = 0.10mol

[HA] = 0.0387 moles = H₂PO₄⁻ moles

That means moles of HPO₄²⁻ are 0.10mol - 0.0387moles = 0.0613 moles

The moles of NaOH needed to convert all H₃PO₄ in H₂PO₄⁻ are 0.10 moles

And moles needed to obtain 0.0613 moles of HPO₄²⁻ are 0.0613 moles

Total moles of NaOH are 0.1613moles * (1L / 1mol) = 0.1613L of 1.00M NaOH

Then, you need to dilute both solutions to 2.00L with distilled water.

4 0
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Varvara68 [4.7K]

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Explanation:

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Answer:

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