What this quiz covers
This quiz focuses on Gibbs Free Energy And Thermodynamic Favorability, giving you a quick way to practice the rules, question types, and explanations that matter most for AP Chemistry.
In a laboratory demonstration, carbon dioxide is converted to solid dry ice:
CO2(g)→CO2(s)
For this phase change, ΔH<0 and ΔS<0. Which statement best describes when deposition is thermodynamically favorable (spontaneous) as written?
AP Chemistry Quiz
Practice Gibbs Free Energy And Thermodynamic Favorability in AP Chemistry with focused quiz questions that help you check what you know, review explanations, and build confidence with test-style prompts.
This quiz focuses on Gibbs Free Energy And Thermodynamic Favorability, giving you a quick way to practice the rules, question types, and explanations that matter most for AP Chemistry.
Try each quiz question before looking at the correct answer. Use the explanations to review missed ideas, then come back to similar questions until the pattern feels familiar.
In a laboratory demonstration, carbon dioxide is converted to solid dry ice:
CO2(g)→CO2(s)
For this phase change, ΔH<0 and ΔS<0. Which statement best describes when deposition is thermodynamically favorable (spontaneous) as written?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. For deposition with ΔH < 0 and ΔS < 0, ΔG = ΔH - TΔS is negative at low temperatures where the negative ΔH outweighs the small positive -TΔS term. At high temperatures, the entropy term dominates, making ΔG positive and the process nonspontaneous. Hence, deposition is thermodynamically favorable only at low temperatures. A tempting distractor is 'Spontaneous at all temperatures,' which is incorrect because it assumes exothermic phase changes are always spontaneous, failing to account for the entropy decrease's growing influence with temperature. Always analyze spontaneity by evaluating ΔG's sign, considering both thermodynamic parameters and temperature.
Consider the reaction
2SO2(g)+O2(g)→2SO3(g)
At 298 K, the value of the Gibbs free energy change for the reaction is ΔG=−71kJ mol−1 (as written). Based on this information, which statement best describes the thermodynamic favorability of the reaction at 298 K?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. A negative ΔG (−71kJ/mol) at 298 K means the reaction is spontaneous at that temperature. ΔG<0 favors the forward direction thermodynamically. This holds regardless of rate. A tempting distractor is choice B, 'Thermodynamically unfavorable (nonspontaneous) at 298 K,' perhaps from misinterpreting the sign. Use given ΔG values directly to assess favorability at specified conditions.
A reaction has ΔH<0 and ΔS<0. Which statement best describes its thermodynamic favorability at high temperature?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. With ΔH < 0 and ΔS < 0, ΔG = ΔH - TΔS becomes positive at high temperatures as -TΔS grows large positive. At low T, ΔG is negative. This shows nonspontaneity at high T. A tempting distractor is choice A, 'Spontaneous at all temperatures,' based on the misconception that exothermic reactions are invariably spontaneous. Evaluate ΔG at specific temperatures to ascertain thermodynamic behavior.
A student studies the dissolution process
NH4NO3(s)→NH4+(aq)+NO3−(aq)
For this process, ΔH>0 and ΔS>0. Under which temperature condition, if any, is the process thermodynamically favorable (spontaneous) based on ΔG=ΔH−TΔS?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. ΔG = ΔH - TΔS determines spontaneity if negative. For this dissolution with ΔH > 0 and ΔS > 0, at high temperatures, TΔS exceeds ΔH, making ΔG negative. At low T, it's positive and nonspontaneous. A tempting distractor is choice C, 'Spontaneous at all temperatures,' which ignores the need for high T to overcome positive ΔH. Apply the ΔG equation to find temperature thresholds for phase or dissolution processes.
A reaction has ΔH<0 and ΔS>0. Which statement best describes its thermodynamic favorability at any temperature?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. When ΔH < 0 and ΔS > 0, ΔG = ΔH - TΔS is always negative, as both terms contribute negatively. Negative ΔH and negative -TΔS favor spontaneity at all temperatures. Entropy's effect strengthens with T. A tempting distractor is choice A, 'Spontaneous only at low temperature,' mistakenly prioritizing enthalpy over entropy at high T. Classify reactions by ΔH and ΔS signs to predict ΔG behavior across temperatures.
For the reaction N2(g)+O2(g)→2NO(g), ΔH>0 and ΔS<0. Which statement best describes the thermodynamic favorability of the reaction as written?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, determines spontaneity, where ΔG < 0 indicates a spontaneous reaction. For this reaction with ΔH > 0 and ΔS < 0, both terms oppose: positive ΔH and positive -TΔS make ΔG always positive. Thus, the reaction is nonspontaneous at all temperatures. A tempting distractor is choice A, which incorrectly suggests spontaneity at high temperatures, assuming entropy drives it despite negative ΔS. Always use ΔG to judge spontaneity, not catalysts which affect only rate.
Consider the reaction N2(g)+3H2(g)→2NH3(g). For this process, ΔH<0 and ΔS<0. Under which conditions is the reaction thermodynamically favorable (spontaneous)?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, determines spontaneity, where ΔG < 0 indicates a spontaneous reaction. For this reaction with ΔH < 0 and ΔS < 0, ΔG = ΔH - TΔS shows that the negative ΔH favors spontaneity, but the negative ΔS makes -TΔS positive, opposing it. At low temperatures, the TΔS term is small, so ΔG is negative and the reaction is spontaneous; at high temperatures, the TΔS term dominates, making ΔG positive. A tempting distractor is choice A, which incorrectly assumes that exothermic reactions are always spontaneous, ignoring the entropy contribution at higher temperatures. Remember that spontaneity depends on the sign of ΔG, not on whether the reaction is exothermic alone.
A sample of solid ammonium nitrate dissolves in water: NH4NO3(s)→NH4+(aq)+NO3−(aq). For this process, ΔH>0 and ΔS>0. Under which conditions is the dissolution thermodynamically favorable (spontaneous)?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, determines spontaneity, where ΔG < 0 indicates a spontaneous process. For this dissolution with ΔH > 0 and ΔS > 0, ΔG = ΔH - TΔS shows that the positive ΔH opposes spontaneity, but the positive ΔS makes -TΔS negative, favoring it. At high temperatures, the TΔS term dominates, making ΔG negative and the process spontaneous; at low temperatures, ΔH dominates, making ΔG positive. A tempting distractor is choice A, which incorrectly assumes endothermic processes are nonspontaneous at all temperatures, disregarding the entropy increase. Always evaluate spontaneity based on ΔG, not just the sign of ΔH.
A reaction has ΔG=+12 kJ mol−1 at 298 K and 1 bar. Which statement best describes the thermodynamic favorability of the reaction as written under these conditions?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, directly determines spontaneity, with ΔG < 0 for spontaneous reactions, ΔG > 0 for nonspontaneous, and ΔG = 0 for equilibrium. Here, ΔG = +12 kJ mol⁻¹ indicates the reaction is nonspontaneous under the given conditions. This positive ΔG means the reverse reaction would be favored. A tempting distractor is choice A, which mistakenly assumes positive ΔG means spontaneous, confusing the sign convention for ΔG. Always verify spontaneity by checking if ΔG is negative, not by confusing it with reaction rate.
The reaction H2(g)+Cl2(g)→2HCl(g) has ΔH<0 and ΔS<0. Under which conditions is the reaction thermodynamically favorable (spontaneous)?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, determines spontaneity, where ΔG < 0 indicates a spontaneous reaction. For this reaction with ΔH < 0 and ΔS < 0, ΔG = ΔH - TΔS means negative ΔH favors, but positive -TΔS opposes. At low temperatures, ΔG is negative; at high temperatures, it's positive. A tempting distractor is choice B, which assumes all exothermic reactions are spontaneous at all temperatures, ignoring entropy. Spontaneity depends on ΔG, not reaction speed.
The dissolution of calcium chloride in water is represented as CaCl2(s)→Ca2+(aq)+2Cl−(aq). For this process, ΔH<0 and ΔS>0. Which statement best describes the thermodynamic favorability of the dissolution as written?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. The Gibbs free energy change, ΔG, determines spontaneity, where ΔG < 0 indicates a spontaneous process. For this dissolution with ΔH < 0 and ΔS > 0, both terms favor: negative ΔH and negative -TΔS ensure ΔG < 0 always. Thus, it's spontaneous at all temperatures. A tempting distractor is choice A, which assumes negative ΔH means nonspontaneous, reversing the enthalpy effect. Remember, spontaneity depends on ΔG, not catalysts which affect kinetics.
For the reaction 2NO2(g)→2NO(g)+O2(g), ΔH>0 and ΔS>0. Which statement best describes the thermodynamic favorability (spontaneity) of the reaction as written?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For NO₂ decomposition, we have ΔH > 0 (endothermic) and ΔS > 0 (increase in entropy as 2 moles of gas form 3 moles). Using ΔG = ΔH - TΔS, when both terms are positive, spontaneity depends on their relative magnitudes. At low temperatures, the positive ΔH dominates over the small TΔS term, making ΔG positive and the reaction nonspontaneous. At high temperatures, the TΔS term becomes large enough to overcome the positive ΔH, making ΔG negative and the reaction spontaneous. Choice E incorrectly states that negative ΔS would make the reaction spontaneous, but with positive ΔH, this would make it nonspontaneous at all temperatures. Remember: when ΔH > 0 and ΔS > 0, reactions become spontaneous only at high temperatures.
The decomposition reaction CaCO3(s)→CaO(s)+CO2(g) has ΔH>0 and ΔS>0. At what temperature conditions is this process thermodynamically favorable (spontaneous) as written?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For calcium carbonate decomposition, we have ΔH > 0 (endothermic) and ΔS > 0 (increase in entropy due to gas formation). Using ΔG = ΔH - TΔS, when both terms are positive, the reaction's spontaneity depends on their relative magnitudes. At low temperatures, the positive ΔH dominates over the small TΔS term, making ΔG positive and the reaction nonspontaneous. At high temperatures, the TΔS term becomes large enough to overcome the positive ΔH, making ΔG negative and the reaction spontaneous. Choice E incorrectly suggests that a negative ΔS would make the reaction spontaneous, but this would actually make it nonspontaneous at all temperatures when combined with positive ΔH. Remember: when ΔH > 0 and ΔS > 0, reactions become spontaneous only at high temperatures where the entropy term dominates.
A process has ΔH>0 and ΔS<0 under the stated conditions. Which statement best describes the thermodynamic favorability (spontaneity) of this process?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. With ΔH > 0 (endothermic) and ΔS < 0 (decrease in entropy), we can analyze using ΔG = ΔH - TΔS. The positive ΔH contributes positively to ΔG, making the process less favorable. The negative ΔS means -TΔS is positive (since -T × negative = positive), also contributing positively to ΔG. Since both terms in the ΔG equation are positive regardless of temperature, ΔG will always be positive, making the process nonspontaneous at all temperatures. Choice E incorrectly suggests that positive ΔH could make a process spontaneous, but positive ΔH actually opposes spontaneity. Remember: when ΔH > 0 and ΔS < 0, both terms work against spontaneity, making the process nonspontaneous at all temperatures.
When NH4NO3(s) dissolves in water to form an aqueous solution, the process has ΔH>0 and ΔS>0. Under which conditions is the dissolution thermodynamically favorable (spontaneous)?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For ammonium nitrate dissolution, we have ΔH > 0 (endothermic) and ΔS > 0 (increase in entropy as solid dissolves). Using ΔG = ΔH - TΔS, both terms are positive, so spontaneity depends on temperature. At low temperatures, the positive ΔH dominates over the small TΔS term, making ΔG positive and dissolution nonspontaneous. At high temperatures, the TΔS term becomes large enough to overcome the positive ΔH, making ΔG negative and dissolution spontaneous. Choice E incorrectly implies that only the sign of ΔH determines spontaneity, but with positive ΔS, an endothermic process can still be spontaneous at sufficiently high temperatures. Remember: when ΔH > 0 and ΔS > 0, processes become spontaneous at high temperatures where entropy dominates.
For the reaction N2(g)+3H2(g)→2NH3(g), ΔH<0 and ΔS<0. Under which conditions is the reaction thermodynamically favorable (spontaneous) as written?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For the ammonia synthesis reaction, we have ΔH < 0 (exothermic) and ΔS < 0 (decrease in entropy due to fewer moles of gas products). Using ΔG = ΔH - TΔS, when both ΔH and ΔS are negative, the -TΔS term becomes positive, opposing the negative ΔH. At low temperatures, the TΔS term is small, so the negative ΔH dominates, making ΔG negative and the reaction spontaneous. At high temperatures, the positive TΔS term becomes large enough to overcome the negative ΔH, making ΔG positive and the reaction nonspontaneous. Choice E incorrectly confuses reaction rate with thermodynamic favorability—spontaneity depends on ΔG, not how fast a reaction proceeds. Remember: when ΔH < 0 and ΔS < 0, reactions are spontaneous only at low temperatures where the enthalpy term dominates.
For the reaction 2H2(g)+O2(g)→2H2O(l), ΔH<0 and ΔS<0. Which statement best describes when the reaction is thermodynamically favorable (spontaneous) as written?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For water formation from gases, we have ΔH < 0 (highly exothermic) and ΔS < 0 (decrease in entropy as gases form liquid). Using ΔG = ΔH - TΔS, when both terms are negative, the -TΔS becomes positive, opposing the negative ΔH. At low temperatures, the TΔS term is small, so the negative ΔH dominates, making ΔG negative and the reaction spontaneous. At high temperatures, the positive TΔS term becomes large enough to overcome the negative ΔH, making ΔG positive and the reaction nonspontaneous. Choice E incorrectly relates reaction speed to spontaneity—thermodynamic favorability depends on ΔG, not kinetics. Remember: when ΔH < 0 and ΔS < 0, reactions are spontaneous only at low temperatures.
The process CO2(g)→CO2(s) (deposition) at 1 atm has ΔH<0 and ΔS<0. Which statement best describes when this process is thermodynamically favorable (spontaneous)?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For the deposition CO₂(g) → CO₂(s), we have ΔH < 0 (exothermic) and ΔS < 0 (gas to solid). Using ΔG = ΔH - TΔS, at low temperatures, the negative ΔH term dominates over the small positive -TΔS term, making ΔG < 0 and the process spontaneous. At high temperatures, the -TΔS term becomes large and positive, making ΔG > 0 and deposition nonspontaneous. Choice C incorrectly assumes that all exothermic processes are spontaneous at all temperatures, ignoring the unfavorable entropy decrease. The principle is that phase transitions with ΔH < 0 and ΔS < 0 favor the more ordered phase at low temperatures.
The reaction 2NO2(g)→N2O4(g) is exothermic (ΔH<0) and results in fewer moles of gas, so ΔS<0. Based on these signs, which statement best describes the thermodynamic favorability of the reaction?
Explanation: This question tests understanding of Gibbs free energy and thermodynamic favorability. For the dimerization reaction 2NO₂(g) → N₂O₄(g), we have ΔH < 0 (exothermic) and ΔS < 0 (fewer moles of gas). Using ΔG = ΔH - TΔS, at low temperatures, the negative ΔH term dominates over the small positive -TΔS term, making ΔG < 0 and the reaction spontaneous. At high temperatures, the -TΔS term becomes large and positive, potentially making ΔG > 0 and the reaction nonspontaneous. Choice A incorrectly assumes that all exothermic reactions are spontaneous at all temperatures, ignoring the unfavorable entropy change. The principle is that reactions with ΔH < 0 and ΔS < 0 are spontaneous only at temperatures below T = ΔH/ΔS.
A student studies the reaction
2NO(g)+O2(g)→2NO2(g)
Thermodynamic signs for the reaction are ΔH<0 and ΔS<0. Under which conditions is the reaction thermodynamically favorable (spontaneous)?
Explanation: This question assesses the skill of Gibbs free energy and thermodynamic favorability. Spontaneity is governed by ΔG=ΔH−TΔS, and for ΔH<0 and ΔS<0, ΔG is negative when ∣ΔH∣>T∣ΔS∣, which happens at low temperatures. At high temperatures, the −TΔS term becomes more positive, making ΔG positive and the reaction nonspontaneous. Therefore, the reaction is thermodynamically favorable only at low temperatures. A tempting distractor is 'Spontaneous at all temperatures,' which is incorrect because it assumes exothermic reactions are always spontaneous, disregarding the negative entropy effect at high temperatures. Remember, spontaneity depends on the sign of ΔG, not solely on the sign of ΔH.