All flashcards
Flashcard 1: What condition on ΔG indicates a process is thermodynamically spontaneous at constant T and P?
Answer: ΔG<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 indicates a process is at equilibrium (no net change) at constant T and P?
Answer: ΔG=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?
Answer: ΔG>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 for a reaction with ΔH<0 and ΔS>0 at any T.
Answer: ΔG<0 at all T. 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 K?
Answer: K 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∘ when K<1?
Answer: ΔG∘>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?
Answer: ΔG<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?
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 corresponds to an exothermic reaction?
Answer: ΔH<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 and on Ea?
Answer: ΔG unchanged; Ea 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, for a process at constant T and P?
Answer: ΔG=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∘=−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 Q?
Answer: ΔG=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 indicates an increase in entropy (greater dispersal of energy/microstates)?
Answer: ΔS>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, Ea, 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∘ when K>1?
Answer: ΔG∘<0. An equilibrium constant greater than one indicates product-favored reactions, corresponding to negative standard free energy change.
Flashcard 18: Which inequality between Q and K makes ΔG negative (net forward reaction favored)?
Answer: Q<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 and maximum nonexpansion work, wmax, at constant T and P?
Answer: ΔG=−wmax. Gibbs free energy change represents the maximum reversible work extractable, excluding pressure-volume work, under isothermal-isobaric conditions.
Flashcard 20: Find ΔG given ΔH=10 kJ/mol, ΔS=20 J/(mol\cdotK), T=300 K.
Answer: ΔG=4 kJ/mol. Convert ΔS to kJ/mol·K, compute TΔS=6 kJ/mol, then subtract from ΔH using the Gibbs free energy equation.
Flashcard 21: Identify when ΔG is negative if ΔH>0 and ΔS>0.
Answer: Negative at high T. At high temperatures, the large negative −TΔS term overcomes the positive enthalpy, making free energy negative.
Flashcard 22: Identify when ΔG is negative if ΔH<0 and ΔS<0.
Answer: Negative at low T. At low temperatures, the negative enthalpy term dominates over the smaller positive −TΔS contribution in the Gibbs equation.
Flashcard 23: Which inequality between Q and K makes ΔG positive (net reverse reaction favored)?
Answer: Q>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 for a reaction with ΔH>0 and ΔS<0 at any T.
Answer: ΔG>0 at all T. Positive enthalpy and negative entropy ensure the Gibbs free energy remains positive, preventing spontaneity at any temperature.