Kp: Equilibrium Constant in Terms of Partial Pressures - 7.1.3 | Unit 7: Equilibrium | IB 11 Chemistry
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Kp: Equilibrium Constant in Terms of Partial Pressures

7.1.3 - Kp: Equilibrium Constant in Terms of Partial Pressures

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Introduction to Kp

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Teacher
Teacher Instructor

Today, we're discussing the equilibrium constant Kp, which is crucial for understanding gas-phase reactions. Kp gives us a way to express the equilibrium in terms of the partial pressures of the gases involved. Can anyone tell me what a partial pressure is?

Student 1
Student 1

Isn't it the pressure that a particular gas in a mixture would exert if it occupied the entire volume alone?

Teacher
Teacher Instructor

Exactly right, Student_1! Each gas in a mixture contributes to the total pressure, and its portion is called its partial pressure. For a reaction like a A(g) + b B(g) β‡Œ c C(g) + d D(g), we express Kp as Kp = (P_C^c β€’ P_D^d) / (P_A^a β€’ P_B^b). Get that? Let’s break it down further.

Student 2
Student 2

So, Kp relates these partial pressures? How does it work?

Teacher
Teacher Instructor

Yes! Kp relates to the concentrations expressed in terms of partial pressures. It's key in predicting the extent of the reaction. Remember, in gas reactions, Kp helps us see how far a reaction goes at equilibrium. Now, can anyone share a situation in everyday life where gas pressures are important?

Kp and Kc Relationship

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Teacher
Teacher Instructor

Now, let’s discuss the relationship between Kp and Kc. They are linked by the equation Kp = Kc (R T)^Ξ”n. Who remembers what R and T represent?

Student 3
Student 3

R is the gas constant, and T is the temperature in Kelvin!

Teacher
Teacher Instructor

Correct! And what about Ξ”n? Can anyone explain what that denotes?

Student 4
Student 4

Ξ”n is the change in the number of moles of gas. It's the moles of products minus the moles of reactants, right?

Teacher
Teacher Instructor

Yes, exactly! It helps determine how changes in temperature will affect our reaction's equilibrium position. If Ξ”n is positive, it means we have more gaseous products than reactants, and that can change how Kp behaves at different temperatures. Let’s apply this to an example next.

Practical Example – Haber Process

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Teacher
Teacher Instructor

Let’s consider a practical example: the Haber process. It looks like Nβ‚‚(g) + 3 Hβ‚‚(g) β‡Œ 2 NH₃(g). Can anyone tell me how to compute Ξ”n here?

Student 1
Student 1

We look at the moles on product side, which is 2, and the reactants side, which is 4. So, Ξ”n = 2 - 4 = -2.

Teacher
Teacher Instructor

Great job! Since Ξ”n is -2, how do you think this affects Kp when the temperature changes?

Student 2
Student 2

If we increase the temperature, Kp will decrease because there's less product compared to reactant moles!

Teacher
Teacher Instructor

Exactly! And this implies that Kp is sensitive to temperature changes, affecting our reactions. Any questions about how Kp is applied?

Calculating Kp vs. Kc

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Teacher
Teacher Instructor

Now that we’ve discussed the theory, let’s apply this knowledge to a calculation. If we know Kc for a reaction at a certain temperature, how do we find Kp?

Student 3
Student 3

We use the formula Kp = Kc (R T)^Ξ”n. Do we have an example?

Teacher
Teacher Instructor

Absolutely! Say Kc for a reaction is 0.5, R = 0.0821 L atm mol⁻¹ K⁻¹, T = 298K, and Ξ”n = -1. Let’s calculate Kp together!

Student 4
Student 4

We plug in the numbers: Kp = 0.5 Γ— (0.0821 Γ— 298)^-1. The calculations seem tricky; can we break it down further?

Teacher
Teacher Instructor

Of course! First calculate the value of (0.0821 Γ— 298), then raise this to the power of -1. Lastly, multiply it by 0.5. Try it out, and we’ll review the results! This practice clearly shows the connection between Kp and Kc.

Summary of Kp Concepts

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Teacher
Teacher Instructor

To summarize today’s lesson, we explored Kp and its expression in terms of partial pressures, the relationship between Kp and Kc, and how changes in temperature and Ξ”n affect Kp. Why is understanding Kp relevant?

Student 1
Student 1

It helps predict the behavior of gas-phase chemical reactions in various conditions!

Student 2
Student 2

And it's crucial for optimizing industrial processes, right?

Teacher
Teacher Instructor

Exactly! Kp is vital in both theoretical and practical scenarios. Always remember Kp connects us directly to how gaseous equilibria work.

Introduction & Overview

Read summaries of the section's main ideas at different levels of detail.

Quick Overview

This section details the concept of the equilibrium constant Kp, which expresses equilibrium in gas-phase reactions in terms of partial pressures.

Standard

Kp is defined for gas reactions using partial pressures, providing a relationship between Kp and Kc through the gas constant and temperature. Key calculations involve determining the change in moles of gas, Ξ”n, which helps understand how changes in conditions like temperature affect equilibrium.

Detailed

Detailed Summary

In gas-phase chemical reactions, the equilibrium constant can be expressed in terms of partial pressures, known as Kp. For a general reaction of gases represented as:

a A(g) + b B(g) β‡Œ c C(g) + d D(g)

the equilibrium constant Kp is given by:

Kp = (P_C^c β€’ P_D^d) / (P_A^a β€’ P_B^b)

Here, P_X indicates the partial pressure of each gas species. A notable relationship exists between Kp and the equilibrium constant based on concentrations, Kc, expressed as:

Kp = Kc (R T)^Ξ”n

where R is the universal gas constant, T is the temperature in Kelvin, and Ξ”n is the difference in moles of gaseous products and reactants defined as:

Ξ”n = (c + d) - (a + b)

This relationship implies that changes in temperature can impact Kp, especially depending on whether there are more gaseous products or reactants at equilibrium. For instance, when considering the Haber process:

Nβ‚‚(g) + 3 Hβ‚‚(g) β‡Œ 2 NH₃(g)

the total moles shift when forming ammonia, indicating a negative Ξ”n, thus affecting the Kp value as the temperature varies. This section emphasizes the importance of Kp in understanding gas-phase equilibria and making predictions regarding the behavior of such systems.

Audio Book

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Definition of Kp

Chapter 1 of 3

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Chapter Content

For gas‐phase reactions, it is often useful to express the equilibrium in terms of partial pressures (in atm or bar). For a gas reaction:
a A(g) + b B(g) β‡Œ c C(g) + d D(g)
we define
Kp = (P_C^c β€’ P_D^d) / (P_A^a β€’ P_B^b)
where P_X is the partial pressure of species X (in atm or another consistent unit).

Detailed Explanation

Kp is a way to express the equilibrium constant for gas-phase reactions using the partial pressures of the reactants and products. Partial pressure is the pressure that a single gas would exert if it occupied the entire volume alone. In the equation, a, b, c, and d represent the stoichiometric coefficients from the balanced chemical reaction. This equation allows us to understand the relationship between different gases at equilibrium.

Examples & Analogies

Imagine a balloon filled with different gases. Each gas has its own space and pressure, like people in a crowded room. The total pressure inside the balloon is a sum of the pressures exerted by each gas. Kp allows us to analyze how these individual pressures contribute to the overall balance of the reaction occurring inside the balloon.

Relation Between Kp and Kc

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Chapter Content

Relation between Kp and Kc: For reactions involving gases, Kp and Kc are related by the equation:
Kp = Kc (R T)^Ξ”n
where:
β—‹ R is the universal gas constant (0.08206 L atm mol⁻¹ K⁻¹ when pressures in atm and volumes in liters).
β—‹ T is the absolute temperature in kelvins (K).
β—‹ Ξ”n (delta n) = (c + d + …) – (a + b + …) = total moles of gaseous products minus total moles of gaseous reactants.

Detailed Explanation

Kp and Kc are two ways to express the equilibrium constant, depending on whether we use partial pressures (Kp) or concentrations (Kc). The equation shows how they relate. The term (R T)^Ξ”n considers the effect of temperature and the number of moles of gaseous reactants and products. Ξ”n helps us understand how the balance shifts based on the number of gases involved in the reaction.

Examples & Analogies

Think of Kp and Kc like two different languages describing the same story. Translation between them requires knowing how many characters (moles) are in the story and the style of writing (pressure or concentration). Just as certain phrases make more sense in one language, some reactions are easier to describe using partial pressures while others rely on concentrations.

Example of Kp Calculation

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Chapter Content

Example: Consider the Haber process simplified to:
Nβ‚‚(g) + 3 Hβ‚‚(g) β‡Œ 2 NH₃(g)
For this reaction:
β—‹ Ξ”n = (2 mol NH₃) – (1 mol Nβ‚‚ + 3 mol Hβ‚‚) = 2 – 4 = –2.
β—‹ Thus, Kp = Kc (R T)^(–2). Since Ξ”n is negative, as T increases, (R T)^(–2) decreases, so Kp will be smaller relative to Kc.

Detailed Explanation

In the Haber process, we have a balanced chemical equation that tells us about the reaction of nitrogen and hydrogen gas to form ammonia. By calculating Ξ”n, we see that we have more moles of reactants than products, indicating that the equilibrium will shift based on the reaction's temperature. The negative Ξ”n impacts the relationship between Kp and Kc, showing that as temperature increases, Kp decreases relative to Kc, meaning the equilibrium favors the reactants.

Examples & Analogies

Imagine cooking with a lid on a pot. At first, steam (product) builds up, but if we take the lid off (increasing temperature by letting gas escape), less steam can form compared to the initial water (reactants). In the Haber process, removing an 'external lid' of pressure shifts equilibrium back toward nitrogen and hydrogen instead of ammonia, similar to how temperature changes affect steam production in cooking.

Key Concepts

  • Kp: The equilibrium constant represented in terms of partial pressures of gaseous reactants and products.

  • Relationship Between Kp and Kc: Kp is related to Kc through the equation Kp = Kc (R T)^Ξ”n.

  • Ξ”n: The difference in moles of gaseous products and reactants, crucial for understanding reaction shifts.

Examples & Applications

The Haber process exemplifies Kp calculations, as seen when determining ammonia formation versus its reactants’ pressures.

For the reaction Nβ‚‚(g) + 3 Hβ‚‚(g) β‡Œ 2 NH₃(g), Ξ”n = -2, indicating that increasing temperature decreases Kp.

Memory Aids

Interactive tools to help you remember key concepts

🎡

Rhymes

In reactions where gases flow, Kp helps us see which way they'll go.

πŸ“–

Stories

Imagine Kp as a helpful guide on a gas journey, determining which gases are strong and making sure the equilibrium is just right.

🧠

Memory Tools

Kp = Keep Pouring the gas until equilibrium is found!β€”the 'K' reminding us of the equilibrium concept.

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Acronyms

Kp = Keep products if Ξ”n is positive.

Flash Cards

Glossary

Kp

Equilibrium constant for gas-phase reactions expressed in terms of partial pressures.

Partial Pressure

The pressure exerted by a single gas in a mixture.

Ξ”n

Change in the number of moles of gases, calculated as moles of products minus moles of reactants.

R

Universal gas constant, used in calculations involving gas behavior.

Temperature

A measure of the kinetic energy of particles, impacting reaction rates and equilibrium constants.

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