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QveST [7]
2 years ago
8

Consider the reaction: 2 H2O (g)-->2 H2 (g) + O2 (g). ΔH=483.6 Kj/mol. If 2 moles of H2O (g) are converted H2(g) and O2(g) ag

ainst a pressure of 1 atm at 125 degrees Celcius what is ΔE of reaction?
Chemistry
2 answers:
denis-greek [22]2 years ago
5 0
DE = dH - PdV 

<span>2 H2O(g) → 2 H2(g) + O2(g) </span>

<span>You can see that there are 2 moles of gas in the reactants and 3 moles of gas in the products. </span>

<span>1 moles of ideal gas occupies the same volume as 1 mole of any other ideal gas under the same conditions of temp and pressure. </span>

<span>Since it is done under constant temp and pressure that means the volume change will be equal to the volume of 1 mole of gas </span>

<span>2 moles reacts to form 3 moles </span>

<span>The gas equation is </span>

<span>PV = nRT </span>
<span>P = pressure </span>
<span>V = volume (unknown) </span>
<span>n = moles (1) </span>
<span>R = gas constant = 8.314 J K^-1 mol^-1 </span>
<span>- the gas constant is different for different units of temp and pressure (see wikki link) in this case temp and pressure are constant, and we want to put the result in an equation that has Joules in it, so we select 8.314 JK^-1mol^-1) </span>
<span>T = temp in Kelvin (kelvin = deg C + 273.15 </span>
<span>So T = 403.15 K </span>

<span>Now, you can see that PV is on one side of the equation, and we are looking to put PdV in our dE equation. So we can say </span>

<span>dE = dH -dnRT (because PV = nRT) </span>

<span>Also, since the gas constant is in the unit of Joules, we need to convert dH to Joules </span>

<span>dH = 483.6 kJ/mol = 483600 Joules/mol </span>

<span>dE = 483600 J/mol - (1.0 mol x 8.314 J mol^-1K-1 x 403.15 K) </span>
<span>dE = 483600 J/mol - 3351.77 J </span>
<span>dE = 480248.23 J/mol </span>
<span>dE = 480.2 kJ/mol </span>
jasenka [17]2 years ago
3 0

Answer : The value of \Delta E of the reaction is, 480.29 KJ.

Explanation :

Formula used :

\Delta E=\Delta H-\Delta n_g\times RT

where,

\Delta E = internal energy of the reaction = ?

\Delta H = enthalpy of the reaction = 483.6 KJ/mole = 483600 J

\Delta n_g = change in the moles of the reaction = Moles of product - Moles of reactant = 3 - 2 = 1 mole

R = gas constant = 8.314 J/mole.K

T = temperature = 125^oC=273+125=398K

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

\Delta E=483600J-(1mole\times 8.314J/mole.K\times 398K)

\Delta E=480291.028J

\Delta E=480.29KJ

Therefore, the value of \Delta E of the reaction is, 480.29 KJ.

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Calculate the pH of a solution that contains 2.7 M HF and 2.7 M HOC6H5. Also, calculate the concentration of OC6H5- in this solu
borishaifa [10]

Answer:

\large \boxed{\mathbf{1.36; 3.6 \times 10^{\mathbf{-9}}}\textbf{mol/L}}

Explanation:

The HF is about five million times as strong as phenol, so it will be by far the major contributor of hydronium ions. We can ignore the contribution from the phenol.

1 .Calculate the hydronium ion concentration

We can use an ICE table to organize the calculations.

                    HF + H₂O ⇌ H₃O⁺ + F⁻

I/mol·L⁻¹:       2.7                   0       0

C/mol·L⁻¹:      -x                   +x      +x

E/mol·L⁻¹:   2.7 - x                 x        x

K_{\text{a}} = \dfrac{\text{[H}_{3}\text{O}^{+}] \text{F}^{-}]} {\text{[HF]}} = 7.2 \times 10^{-4}\\\\\dfrac{x^{2}}{2.7 - x} = 7.2 \times 10^{-4}\\\\\text{Check for negligibility of }x\\\\\dfrac{2.7}{7.2 \times 10^{-4}} = 4000 > 400\\\\\therefore x \ll 2.7\\\dfrac{x^{2}}{2.7} = 7.2 \times 10^{-4}\\\\x^{2} = 2.7 \times 7.2 \times 10^{-4} = 1.94 \times 10^{-3}\\x = 0.0441\\\text{[H$_{3}$O$^{+}$]}= \text{x mol$\cdot$L$^{-1}$} = \text{0.0441 mol$\cdot$L$^{-1}$}

2. Calculate the pH

\text{pH} = -\log{\rm[H_{3}O^{+}]} = -\log{0.0441} = \large \boxed{\mathbf{1.36}}

3. Calculate [C₆H₅O⁻]

C₆H₅OH + H₂O ⇌ C₆H₅O⁻ + H₃O⁺

     2.7                         x        0.0441

K_{\text{a}} = \dfrac{0.0441x} {2.7} = 1.6 \times 10^{-10}\\\\0.0441x = 1.6 \times 10^{-10}\\x = \dfrac{1.6 \times 10^{-10}}{0.0441} = \mathbf{3.6 \times 10^{\mathbf{-9}}}\textbf{ mol/L}\\\text{The concentration of phenoxide ion is $\large \boxed{\mathbf{3.6 \times 10^{\mathbf{-9}}}\textbf{ mol/L}}$}

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When preparing the diazonium salt, the solution is tested with potassium iodide-starch paper. a positive test is the immediate f
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KI-starch paper allows the detection of strong oxidizers such as nitrite. It is used here to control diazotization of 4-nitroaniline. Nitrite oxidizes potassium iodide in order to form elemental iodine which reacts with starch to a blue-violet complex. With KI-starch paper, enough sodium nitrite is added to produce nitrous acid, which <span>then will react with 4-nitroaniline to form a diazonium salt.</span>
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Sulfuryl dichloride is formed when sulfur dioxide reacts with chlorine.
zubka84 [21]

<u>Answer:</u> The value of \Delta G^o of the reaction is 28.38 kJ/mol

<u>Explanation:</u>

For the given chemical reaction:

SO_2(g)+Cl_2(g)\rightarrow SO_2Cl_2(g)

  • The equation used to calculate enthalpy change is of a reaction is:

\Delta H^o_{rxn}=\sum [n\times \Delta H^o_f_{(product)}]-\sum [n\times \Delta H^o_f_{(reactant)}]

The equation for the enthalpy change of the above reaction is:

\Delta H^o_{rxn}=[(1\times \Delta H^o_f_{(SO_2Cl_2(g))})]-[(1\times \Delta H^o_f_{(SO_2(g))})+(1\times \Delta H^o_f_{(Cl_2(g))})]

We are given:

\Delta H^o_f_{(SO_2Cl_2(g))}=-364kJ/mol\\\Delta H^o_f_{(SO_2(g))}=-296.8kJ/mol\\\Delta H^o_f_{(Cl_2(g))}=0kJ/mol

Putting values in above equation, we get:

\Delta H^o_{rxn}=[(1\times (-364))]-[(1\times (-296.8))+(1\times 0)]=-67.2kJ/mol=-67200J/mol

  • The equation used to calculate entropy change is of a reaction is:

\Delta S^o_{rxn}=\sum [n\times \Delta S^o_f_{(product)}]-\sum [n\times \Delta S^o_f_{(reactant)}]

The equation for the entropy change of the above reaction is:

\Delta S^o_{rxn}=[(1\times \Delta S^o_{(SO_2Cl_2(g))})]-[(1\times \Delta S^o_{(SO_2(g))})+(1\times \Delta S^o_{(Cl_2(g))})]

We are given:

\Delta S^o_{(SO_2Cl_2(g))}=311.9J/Kmol\\\Delta S^o_{(SO_2(g))}=248.2J/Kmol\\\Delta S^o_{(Cl_2(g))}=223.0J/Kmol

Putting values in above equation, we get:

\Delta S^o_{rxn}=[(1\times 311.9)]-[(1\times 248.2)+(1\times 223.0)]=-159.3J/Kmol

To calculate the standard Gibbs's free energy of the reaction, we use the equation:

\Delta G^o_{rxn}=\Delta H^o_{rxn}-T\Delta S^o_{rxn}

where,

\Delta H^o_{rxn} = standard enthalpy change of the reaction =-67200 J/mol

\Delta S^o_{rxn} = standard entropy change of the reaction =-159.3 J/Kmol

Temperature of the reaction = 600 K

Putting values in above equation, we get:

\Delta G^o_{rxn}=-67200-(600\times (-159.3))\\\\\Delta G^o_{rxn}=28380J/mol=28.38kJ/mol

Hence, the value of \Delta G^o of the reaction is 28.38 kJ/mol

7 0
3 years ago
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