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  2. MCAT Biological and Biochemical Foundations of Living Systems
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MCAT Biological and Biochemical Foundations of Living Systems Flashcards: 1d Bioenergetics Thermodynamics

Study 1d Bioenergetics Thermodynamics in MCAT Biological and Biochemical Foundations of Living Systems with focused flashcards that help you recognize the idea, recall the key rule, and apply it in practice-style prompts.

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What this deck covers

This deck focuses on 1d Bioenergetics Thermodynamics, giving you a quick way to review the definitions, rules, and examples that matter most for MCAT Biological and Biochemical Foundations of Living Systems.

How to use these flashcards

Work through these flashcards in short sessions. Try to answer each prompt before flipping the card, then revisit any cards you miss until the explanation feels automatic.

MCAT Biological and Biochemical Foundations of Living Systems Flashcards: 1d Bioenergetics Thermodynamics

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QUESTION

What condition on ΔG\Delta GΔG indicates a process is thermodynamically spontaneous at constant TTT and PPP?

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ANSWER

ΔG<0\Delta G < 0ΔG<0. Negative free energy change drives processes toward lower energy states, enabling spontaneity without external input under constant conditions.

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Flashcard 1: What condition on ΔG\Delta GΔG indicates a process is thermodynamically spontaneous at constant TTT and PPP?

Answer: ΔG<0\Delta G < 0ΔG<0. Negative free energy change drives processes toward lower energy states, enabling spontaneity without external input under constant conditions.

Flashcard 2: What condition on ΔG\Delta GΔG indicates a process is at equilibrium (no net change) at constant TTT and PPP?

Answer: ΔG=0\Delta G = 0ΔG=0. At equilibrium, the system's free energy is minimized, resulting in no net driving force for forward or reverse processes.

Flashcard 3: What is the definition of an endergonic reaction in terms of ΔG\Delta GΔG?

Answer: ΔG>0\Delta G > 0ΔG>0. Endergonic processes require free energy input from surroundings to proceed, characterized by a positive change in Gibbs free energy.

Flashcard 4: Identify the sign of ΔG\Delta GΔG for a reaction with ΔH<0\Delta H < 0ΔH<0 and ΔS>0\Delta S > 0ΔS>0 at any TTT.

Answer: ΔG<0\Delta G < 0ΔG<0 at all TTT. With negative enthalpy and positive entropy, both terms in the Gibbs equation contribute to spontaneity regardless of temperature.

Flashcard 5: What is the relationship between spontaneity and rate (kinetics) for a reaction on the MCAT?

Answer: Spontaneous does not imply fast. Thermodynamic spontaneity assesses feasibility based on energy changes, independent of kinetic factors that determine reaction speed.

Flashcard 6: What effect does a catalyst (enzyme) have on the equilibrium constant KKK?

Answer: KKK unchanged. Catalysts equally accelerate forward and reverse rates, maintaining the ratio that defines the equilibrium constant unchanged.

Flashcard 7: What is the sign of ΔG∘\Delta G^\circΔG∘ when K<1K < 1K<1?

Answer: ΔG∘>0\Delta G^\circ > 0ΔG∘>0. An equilibrium constant less than one signifies reactant-favored reactions, resulting in positive standard free energy change.

Flashcard 8: What is the definition of an exergonic reaction in terms of ΔG\Delta GΔG?

Answer: ΔG<0\Delta G < 0ΔG<0. Exergonic processes release free energy to surroundings, driven by a negative change in Gibbs free energy under constant conditions.

Flashcard 9: What is the MCAT-appropriate definition of enthalpy change, ΔH\Delta HΔH?

Answer: Heat transferred at constant pressure. Enthalpy change measures heat exchange during reactions or phase changes when pressure remains constant, as per thermodynamic definitions.

Flashcard 10: What sign of ΔH\Delta HΔH corresponds to an exothermic reaction?

Answer: ΔH<0\Delta H < 0ΔH<0. Exothermic processes release heat to surroundings, reducing the system's internal energy and thus yielding a negative enthalpy change.

Flashcard 11: What effect does a catalyst (enzyme) have on ΔG\Delta GΔG and on EaE_aEa​?

Answer: ΔG\Delta GΔG unchanged; EaE_aEa​ decreased. Catalysts lower the activation energy by stabilizing the transition state, but thermodynamics dictate that free energy difference remains constant.

Flashcard 12: What is the definition of Gibbs free energy change, ΔG\Delta GΔG, for a process at constant TTT and PPP?

Answer: ΔG=ΔH−TΔS\Delta G = \Delta H - T\Delta SΔG=ΔH−TΔS. This equation quantifies the free energy available for work by balancing enthalpy and entropy contributions at constant temperature and pressure.

Flashcard 13: What is the formula linking standard free energy and equilibrium constant?

Answer: ΔG∘=−RTln⁡K\Delta G^\circ = -RT\ln KΔG∘=−RTlnK. This relation connects thermodynamic favorability under standard conditions to the equilibrium constant via temperature and the gas constant.

Flashcard 14: What is the formula for nonstandard free energy change in terms of reaction quotient QQQ?

Answer: ΔG=ΔG∘+RTln⁡Q\Delta G = \Delta G^\circ + RT\ln QΔG=ΔG∘+RTlnQ. This equation adjusts standard free energy for non-equilibrium conditions by incorporating the reaction quotient and thermal energy.

Flashcard 15: What sign of ΔS\Delta SΔS indicates an increase in entropy (greater dispersal of energy/microstates)?

Answer: ΔS>0\Delta S > 0ΔS>0. Positive entropy change signifies increased molecular disorder or more accessible microstates, aligning with the second law of thermodynamics.

Flashcard 16: What is the definition of activation energy, EaE_aEa​, in reaction kinetics?

Answer: Energy barrier to reach the transition state. Activation energy quantifies the kinetic barrier reactants must overcome to form the high-energy transition state in a reaction pathway.

Flashcard 17: What is the sign of ΔG∘\Delta G^\circΔG∘ when K>1K > 1K>1?

Answer: ΔG∘<0\Delta G^\circ < 0ΔG∘<0. An equilibrium constant greater than one indicates product-favored reactions, corresponding to negative standard free energy change.

Flashcard 18: Which inequality between QQQ and KKK makes ΔG\Delta GΔG negative (net forward reaction favored)?

Answer: Q<KQ < KQ<K. When the reaction quotient is below the equilibrium constant, the system shifts forward to minimize free energy.

Flashcard 19: What is the relationship between ΔG\Delta GΔG and maximum nonexpansion work, wmax⁡w_{\max}wmax​, at constant TTT and PPP?

Answer: ΔG=−wmax⁡\Delta G = -w_{\max}ΔG=−wmax​. Gibbs free energy change represents the maximum reversible work extractable, excluding pressure-volume work, under isothermal-isobaric conditions.

Flashcard 20: Find ΔG\Delta GΔG given ΔH=10 kJ/mol\Delta H = 10\ \text{kJ/mol}ΔH=10 kJ/mol, ΔS=20 J/(mol\cdotK)\Delta S = 20\ \text{J/(mol\cdot K)}ΔS=20 J/(mol\cdotK), T=300 KT = 300\ \text{K}T=300 K.

Answer: ΔG=4 kJ/mol\Delta G = 4\ \text{kJ/mol}ΔG=4 kJ/mol. Convert ΔS\Delta SΔS to kJ/mol·K, compute TΔS=6T\Delta S = 6TΔS=6 kJ/mol, then subtract from ΔH\Delta HΔH using the Gibbs free energy equation.

Flashcard 21: Identify when ΔG\Delta GΔG is negative if ΔH>0\Delta H > 0ΔH>0 and ΔS>0\Delta S > 0ΔS>0.

Answer: Negative at high TTT. At high temperatures, the large negative −TΔS-T\Delta S−TΔS term overcomes the positive enthalpy, making free energy negative.

Flashcard 22: Identify when ΔG\Delta GΔG is negative if ΔH<0\Delta H < 0ΔH<0 and ΔS<0\Delta S < 0ΔS<0.

Answer: Negative at low TTT. At low temperatures, the negative enthalpy term dominates over the smaller positive −TΔS-T\Delta S−TΔS contribution in the Gibbs equation.

Flashcard 23: Which inequality between QQQ and KKK makes ΔG\Delta GΔG positive (net reverse reaction favored)?

Answer: Q>KQ > KQ>K. When the reaction quotient exceeds the equilibrium constant, the system favors the reverse direction to reach equilibrium.

Flashcard 24: Identify the sign of ΔG\Delta GΔG for a reaction with ΔH>0\Delta H > 0ΔH>0 and ΔS<0\Delta S < 0ΔS<0 at any TTT.

Answer: ΔG>0\Delta G > 0ΔG>0 at all TTT. Positive enthalpy and negative entropy ensure the Gibbs free energy remains positive, preventing spontaneity at any temperature.