Gibbs Free Energy and Thermodynamic Favorability

Sophie Anderson
7 min read
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Study Guide Overview
This study guide covers thermodynamic favorability and spontaneity of reactions. Key concepts include enthalpy (ΔH°), entropy (ΔS°), and Gibbs Free Energy (ΔG°). It explains how to calculate ΔG° using the formula ΔG° = ΔH° - TΔS° and standard free energies of formation. The guide also discusses conditions influencing spontaneity and distinguishes between entropy-driven and enthalpy-driven reactions, including practice problems and exam tips.
#Thermodynamic Favorability: Is It Going to Happen? 🤔
Hey, future AP Chem master! Let's dive into thermodynamic favorability, which is all about predicting whether a reaction will occur spontaneously. Think of it like this: is the reaction naturally inclined to happen, or does it need a push? Let's find out!
This topic is crucial for understanding reaction spontaneity and equilibrium, which are major themes in AP Chemistry. Expect to see these concepts in both multiple-choice and free-response questions.
#Explaining Thermodynamic Favorability
Thermodynamic favorability helps us determine if a reaction is spontaneous (happens on its own) or nonspontaneous (needs external help). Spontaneous reactions are thermodynamically favorable, while non-spontaneous ones are thermodynamically unfavorable.
Spontaneity is directly linked to the equilibrium constant. A spontaneous reaction tends to favor product formation.
#Enthalpy (ΔH°) and Entropy (ΔS°): The Dynamic Duo
Two main factors determine spontaneity:
- Enthalpy Change (ΔH°): This is the heat change in a reaction.
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Exothermic (ΔH° < 0): System loses heat to surroundings. Think of it as 'heat exiting'. 🔥
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Endothermic (ΔH° > 0): System gains heat from surroundings. Think of it as 'heat entering'. 🧊
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*Caption: Visualizing exothermic and endothermic reactions. Exothermic reactions release heat, while endothermic reactions absorb it.*
2. Entropy Change (ΔS°): This is the change in disorder or randomness of a system. * Positive ΔS°: Disorder increases. More chaos! 🎉 * Negative ΔS°: Disorder decreases. More order. 😥
Reactions that increase entropy are exentropic, and those that decrease entropy are endentropic. These terms are less common on the AP exam but good to know.
#Gibbs Free Energy (ΔG°): The Spontaneity Decider
Gibbs Free Energy (ΔG°) combines enthalpy and entropy to determine spontaneity. The formula is:
Remember the Gibbs Free Energy equation: Good Helpers Take Study (ΔG = ΔH - TΔS). It's a bit silly, but it sticks!
This equation is provided on the AP Chemistry reference sheet, but knowing how to use it is key!
- ΔG° < 0: Reaction is spontaneous (exergonic). Energy is released. ✅
- ΔG° > 0: Reaction is nonspontaneous (endergonic). Energy is absorbed. ❌
#Practice Problem: Let's Calculate ΔG°
Reaction: 2H₂ + N₂ ⇌ N₂H₄
Given:
- ΔH° = 50.6 kJ/mol
- ΔS° = -0.332 kJ/(mol·K)
- T = 25°C (298 K)
Let's plug these values into the Gibbs Free Energy equation:
Since ΔG° is positive, this reaction is nonspontaneous.
Don't forget to convert temperature to Kelvin (K) by adding 273 to the Celsius temperature! This is a frequent error that can cost you points.
#Calculating ΔG° Using Standard Free Energies of Formation
Just like with ΔH° and ΔS°, we can calculate ΔG° using standard free energies of formation:
Caption: Standard free energies of formation are used to calculate the overall Gibbs free energy change for a reaction.
#Conditions for ΔG°: When is it Positive or Negative?
To be spontaneous, a reaction must either:
- Be exothermic (ΔH° < 0)
- Increase entropy (ΔS° > 0)
Let’s analyze the different scenarios:
- ΔH° < 0 and ΔS° > 0: ΔG° is always negative, reaction is always spontaneous. 🎉
- ΔH° > 0 and ΔS° < 0: ΔG° is always positive, reaction is never spontaneous. 😥
- ΔH° < 0 and ΔS° < 0: Spontaneous at low temperatures. 🔥
- ΔH° > 0 and ΔS° > 0: Spontaneous at high temperatures. 🧊
Caption: A handy chart summarizing the conditions for spontaneity based on enthalpy and entropy changes.
#Entropy-Driven vs. Enthalpy-Driven Reactions
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Entropy-Driven: Spontaneity is mainly due to an increase in disorder (ΔS°). Example: Dissolving NaCl (endothermic but spontaneous due to increased entropy). 🧂
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Enthalpy-Driven: Spontaneity is mainly due to a release of heat (ΔH°). Example: Combustion reactions (exothermic and usually spontaneous). 🔥
Think of it this way: Entropy-driven reactions love chaos, while enthalpy-driven reactions love to release heat.
#Final Exam Focus
- High-Priority Topics: Gibbs Free Energy calculations, understanding the relationship between ΔG°, ΔH°, and ΔS°, and predicting spontaneity based on these values.
- Common Question Types: Calculating ΔG° using the equation or standard free energies of formation, determining spontaneity based on given ΔH° and ΔS° values, and identifying whether a reaction is entropy- or enthalpy-driven.
- Time Management: Practice calculations to build speed. Focus on understanding the concepts rather than just memorizing formulas. Be careful with unit conversions!
- Common Pitfalls: Forgetting to convert temperature to Kelvin, mixing up signs in the Gibbs Free Energy equation, and not understanding the conditions for spontaneity.
#Practice Questions
Practice Question
#Multiple Choice Questions
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For a reaction to be spontaneous at all temperatures, which of the following conditions must be met? (A) ΔH > 0, ΔS > 0 (B) ΔH < 0, ΔS < 0 (C) ΔH < 0, ΔS > 0 (D) ΔH > 0, ΔS < 0
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A reaction has a positive enthalpy change and a positive entropy change. Under what conditions will this reaction be spontaneous? (A) Always spontaneous (B) Never spontaneous (C) Spontaneous at high temperatures (D) Spontaneous at low temperatures
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Which of the following processes is most likely to be entropy-driven? (A) Freezing of water (B) Combustion of methane (C) Dissolving of sugar in water (D) Condensation of steam
#Free Response Question
Consider the following reaction:
Given the following thermodynamic data at 298 K:
Substance | ΔH°f (kJ/mol) | S° (J/mol·K) |
---|---|---|
N₂(g) | 0 | 192 |
H₂(g) | 0 | 131 |
NH₃(g) | -46 | 193 |
(a) Calculate the standard enthalpy change, ΔH° for the reaction. (b) Calculate the standard entropy change, ΔS° for the reaction. (c) Calculate the standard Gibbs free energy change, ΔG° for the reaction. (d) Is this reaction spontaneous under standard conditions? Explain. (e) Is this reaction enthalpy-driven or entropy-driven? Explain.
#Scoring Breakdown for FRQ
(a) Calculating ΔH° (2 points)
- 1 point for correct setup: ΔH° = [2(-46)] - [0 + 3(0)]
- 1 point for correct answer: ΔH° = -92 kJ/mol
(b) Calculating ΔS° (2 points)
- 1 point for correct setup: ΔS° = [2(193)] - [192 + 3(131)]
- 1 point for correct answer: ΔS° = -199 J/mol·K or -0.199 kJ/mol·K
(c) Calculating ΔG° (2 points)
- 1 point for correct setup: ΔG° = -92 - (298)(-0.199)
- 1 point for correct answer: ΔG° = -32.6 kJ/mol
(d) Spontaneity (1 point)
- 1 point for stating that the reaction is spontaneous because ΔG° is negative.
(e) Enthalpy-Driven or Entropy-Driven (1 point)
- 1 point for stating that the reaction is enthalpy-driven because both ΔH and ΔG are negative and ΔS is negative.
You've got this! Keep practicing, and you'll ace the AP Chemistry exam! 🎉
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