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ra1l [238]
3 years ago
12

Phosphorus trichloride gas and chlorine gas react to form phosphorus pentachloride gas: PCl3(g)+Cl2(g)⇌PCl5(g). A 7.5-L gas vess

el is charged with a mixture of PCl3(g) and Cl2(g), which is allowed to equilibrate at 450 K. At equilibrium the partial pressures of the three gases are PPCl3 = 0.125atm , PCl2 = 0.155atm , and PPCl5 = 1.90atm Kp= 98.1 What is Kc?
Chemistry
2 answers:
Law Incorporation [45]3 years ago
7 0

Answer:

Kc is 3623

Explanation:

Write out the parameters given:

Volume = 7.5 L,   Kp = 98.1, Partial pressure of PCl_{3} at equilibrium = 0.125 atm,  Partial pressure of Cl_{2} at equilibrium = 0.155 atm, Partial pressure of PCl_{5} at equilibrium = 1.90 atm,

R = 0.08206 L·atm/(mol·K), T = 450 K

Formula to calculate Kc is given below:

K_{p} = K_{c}(RT)^{n}

n is given by the difference between the moles of gaseous products (PCl5) & the moles of gaseous reactants (PCl3) (Cl2) as seen in the chemical reaction PCl_{3} (g) + Cl_{2} (g) ⇌ PCl_{5} (g)

n = 1 - 2 = -1

Substitute the parameters into the equation to solve for Kc, we have:

98.1 = K_c (0.08206 X 450)^{-1}

Kc = 3622.5 ≅ 3623

Kc = <u>3623</u>

Tpy6a [65]3 years ago
5 0

Answer:

The equilibrium constant in terms of concentration that is, K_c=3.6243\times 10^{3} .

Explanation:

PCl_3(g)+Cl_2(g)\rightleftharpoons PCl_5(g)

The relation of K_c\& K_p is given by:

K_p=K_c(RT)^{\Delta n_g}

K_p= Equilibrium constant in terms of partial pressure.=98.1

K_c= Equilibrium constant in terms of concentration  =?

T = temperature at which the equilibrium reaction is taking place.

R = universal gas constant

\Delta n_g = Difference between gaseous moles on product side and reactant side=n_{g,p}-n_{g.r}=1-2=-1

98.1=K_c(RT)^{-1}

98.1 =\frac{K_c}{RT}

K_c=98.1\times 0.0821 L atm/mol K\times 450 K=3,624.30=3.6243\times 10^{3}

The equilibrium constant in terms of concentration that is, K_c=3.6243\times 10^{3} .

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Answer:

<u>The standard enthalpy of reaction = -4854.7kJ</u>

<u>The difference: </u>ΔH-ΔE = Δ(PV) = Δn.R.T = <u>9910.288 J ≈ 9.91 kJ</u>    

Explanation:

<u>The balanced chemical equation for the combustion of heptane</u>:

C₇H₁₆ (l) + 11 O₂ (g) → 7 CO₂ (g) + 8 H₂O (l)

Given: The standard enthalpy of formation (\Delta H _{f}^{\circ }) for: C₇H₁₆ (l) = -187.8 kJ/mol, O₂ (g) = 0 kJ/mol, CO₂ (g) = -393.5 kJ/mol, H₂O (l) = -286 kJ/mol

<u>To calculate the standard enthalpy of reaction (\Delta H _{r}^{\circ }) can be calculated by the Hess's law</u>:

\Delta H _{r}^{\circ } = \left [\sum \nu \cdot\Delta H _{f}^{\circ }(products)  \right ] - \left [\sum \nu\cdot\Delta H _{f}^{\circ }(reactants)  \right ]

Here, \nu is the stoichiometric coefficient

⇒ \Delta H _{r}^{\circ } =

\left [ 7\times \Delta H _{f}^{\circ }\left (CO_{2}\right )+ 8\times \Delta H _{f}^{\circ }\left (H_{2}O \right )\right ]

- \left [1\times \Delta H _{f}^{\circ }\left (C_{7}H_{16}\right ) +11\times \Delta H _{f}^{\circ }\left (O_{2} \right ) \right ]

=\left [ 7\times \left (-393.5 kJ/mol \right )+ 8\times \left (-286 kJ/mol \right )\right ]

-\left [1\times \left (-187.8 kJ/mol \right ) +11\times \left (0 kJ/mol \right ) \right ]

⇒ \Delta H _{r}^{\circ } = \left [ \left (-2754.5 \right )+ \left (-2288 \right )\right ]\left -[ \left (-187.8 \right ) +\left (0 \right )\right ]

⇒ \Delta H _{r}^{\circ } = \left [ -5042.5 ]\left -[ -187.8] = \left ( -4854.7kJ \right )

<u>To calculate the difference: </u>ΔH-ΔE=Δ(PV)

We use the ideal gas equation: P.V = n.R.T

⇒ ΔH-ΔE=Δ(PV) = Δn.R.T

Given: Temperature:T = 298K, R = 8.314 J⋅K⁻¹⋅mol⁻¹

Δn = number of moles of gaseous products - number of moles of gaseous reactants = (7)- (11) = (-4)

⇒ ΔH-ΔE=Δ(PV) = Δn.R.T = (-4 mol) × (8.314 J⋅K⁻¹⋅mol⁻¹) × (298K) = <u>9910.288 J = 9.91 kJ</u>                              (∵ 1 kJ = 1000J )

                                                                             

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