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    Medium MCAT Thermodynamics Practice Questions

    May 17, 202611 min read63 views
    Medium MCAT Thermodynamics Practice Questions

    Medium MCAT Thermodynamics Practice Questions

    Mastering thermodynamics is essential for success on the MCAT, as it governs every biochemical reaction in the human body and every phase change in a beaker. This guide provides comprehensive Medium MCAT Thermodynamics Practice Questions to help you bridge the gap between basic definitions and complex application. By understanding how energy, entropy, and enthalpy interact, you will be better prepared for the Chemical and Physical Foundations of Biological Systems section of the exam.

    Concept Explanation

    MCAT thermodynamics is the study of energy, heat, and work transformations within physical and chemical systems to determine the spontaneity and equilibrium of reactions. At the heart of this subject are the three laws of thermodynamics. The First Law (Conservation of Energy) states that energy cannot be created or destroyed, expressed by the equation ΔU=QW\Delta U = Q - W, where ΔU\Delta U is the change in internal energy, QQ is heat added to the system, and WW is work done by the system. The Second Law introduces entropy (SS), asserting that the total entropy of an isolated system always increases over time, favoring disorder. The Third Law establishes that the entropy of a perfect crystal at absolute zero (0 K) is zero.

    For the MCAT, you must be proficient in calculating Gibbs Free Energy (ΔG\Delta G), which combines enthalpy (ΔH\Delta H) and entropy to predict reaction spontaneity. The relationship is defined as:

    ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S

    A negative ΔG\Delta G indicates a spontaneous (exergonic) reaction, while a positive value indicates a non-spontaneous (endergonic) reaction. Understanding these concepts is often a prerequisite for more advanced topics like Medium MCAT Electrochemistry Practice Questions, where cell potential is directly linked to free energy. Additionally, you should be familiar with calorimetry and Hess’s Law, which allow for the calculation of total enthalpy changes by summing the enthalpies of individual reaction steps. These principles are closely related to Medium MCAT Thermochemistry Practice Questions, which focus specifically on heat transfer during chemical changes.

    Solved Examples

    Review these worked examples to understand the logic required for medium-difficulty thermodynamics problems.

    1. Example: Calculating Gibbs Free Energy
      A specific protein folding reaction has an enthalpy change of 50  kJ/mol-50 \ \text{ kJ/mol} and an entropy change of 0.15  kJ/mol K-0.15 \ \text{ kJ/mol} \cdot \ \text{K}. Is this reaction spontaneous at 300  K300 \ \text{ K}?
      1. Identify the given values: ΔH=50  kJ/mol\Delta H = -50 \ \text{ kJ/mol}, ΔS=0.15  kJ/mol K\Delta S = -0.15 \ \text{ kJ/mol} \cdot \ \text{K}, and T=300  KT = 300 \ \text{ K}.
      2. Apply the formula: ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S.
      3. Substitute the values: ΔG=50(300 ×0.15)\Delta G = -50 - (300 \ \times -0.15).
      4. Calculate: ΔG=50(45)=5  kJ/mol\Delta G = -50 - (-45) = -5 \ \text{ kJ/mol}.
      5. Conclusion: Since ΔG\Delta G is negative, the reaction is spontaneous at this temperature.
    2. Example: Work Done by a Gas
      A gas in a piston expands from 2  L2 \ \text{ L} to 5  L5 \ \text{ L} against a constant external pressure of 3  atm3 \ \text{ atm}. Calculate the work done by the gas in Joules (Note: 1  L atm101.3  J1 \ \text{ L} \cdot \ \text{atm} \approx 101.3 \ \text{ J}).
      1. Use the formula for pressure-volume work: W=PΔVW = P\Delta V.
      2. Find the change in volume: ΔV=5  L2  L=3  L\Delta V = 5 \ \text{ L} - 2 \ \text{ L} = 3 \ \text{ L}.
      3. Calculate work in  L atm\ \text{L} \cdot \ \text{atm}: W=3  atm ×3  L=9  L atmW = 3 \ \text{ atm} \ \times 3 \ \text{ L} = 9 \ \text{ L} \cdot \ \text{atm}.
      4. Convert to Joules: 9 ×101.3911.7  J9 \ \times 101.3 \approx 911.7 \ \text{ J}.
    3. Example: Hess's Law Application
      Find the enthalpy of reaction for A CA \ \rightarrow C given:
      1) A BΔH=+20  kJA \ \rightarrow B \quad \Delta H = +20 \ \text{ kJ}
      2) C BΔH=+5  kJC \ \rightarrow B \quad \Delta H = +5 \ \text{ kJ}
      1. We need to arrange the reactions to get A CA \ \rightarrow C.
      2. Keep reaction (1) as is: A B(ΔH=+20  kJ)A \ \rightarrow B \quad (\Delta H = +20 \ \text{ kJ}).
      3. Reverse reaction (2) to get B CB \ \rightarrow C. When reversing, change the sign of ΔH\Delta H: B C(ΔH=5  kJ)B \ \rightarrow C \quad (\Delta H = -5 \ \text{ kJ}).
      4. Sum the reactions: A+B B+CA + B \ \rightarrow B + C, which simplifies to A CA \ \rightarrow C.
      5. Sum the enthalpies: 20  kJ+(5  kJ)=+15  kJ20 \ \text{ kJ} + (-5 \ \text{ kJ}) = +15 \ \text{ kJ}.

    Practice Questions

    Test your knowledge with these Medium MCAT Thermodynamics Practice Questions. Ensure you pay close attention to units and signs.

    1. A reaction is found to have a positive ΔH\Delta H and a positive ΔS\Delta S. Under what conditions will this reaction be spontaneous?
    2. Calculate the change in internal energy (ΔU\Delta U) for a system that absorbs 500  J500 \ \text{ J} of heat and performs 200  J200 \ \text{ J} of work on its surroundings.
    3. According to the Second Law of Thermodynamics, which of the following must be true for any spontaneous process in an isolated system?

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    1. A 50.0  g50.0 \ \text{ g} sample of copper (specific heat c=0.385  J/g Cc = 0.385 \ \text{ J/g} \cdot ^{\circ}\ \text{C}) is heated from 20 C20^{\circ}\ \text{C} to 80 C80^{\circ}\ \text{C}. How much heat energy was absorbed?
    2. Which thermodynamic state function is used to measure the heat content of a system at constant pressure?
    3. For the reaction N2(g)+3H2(g) 2NH3(g)N_2(g) + 3H_2(g) \ \rightarrow 2NH_3(g), predict the sign of ΔS\Delta S and explain why.
    4. If a reaction has a K>1K_{ \neq} > 1 at a specific temperature, what can be said about the standard Gibbs free energy (ΔG\Delta G^{\circ})?
    5. Compare the entropy of a liquid to its gaseous state at the same temperature. Which is higher and why?
    6. A system undergoes an adiabatic process. If the gas performs work on the surroundings, what happens to the temperature of the system?
    7. Using Hess's Law, calculate the total enthalpy for a reaction that occurs in three steps with ΔH\Delta H values of 120  kJ-120 \ \text{ kJ}, +50  kJ+50 \ \text{ kJ}, and 30  kJ-30 \ \text{ kJ}.

    Answers & Explanations

    1. Answer: At high temperatures.
      According to ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S, if both ΔH\Delta H and ΔS\Delta S are positive, the term TΔS-T\Delta S must be large enough in magnitude to outweigh the positive ΔH\Delta H. This occurs when TT is large.
    2. Answer: +300  J+300 \ \text{ J}.
      Using the First Law: ΔU=QW\Delta U = Q - W. Here, Q=+500  JQ = +500 \ \text{ J} (heat absorbed) and W=+200  JW = +200 \ \text{ J} (work done by the system). Thus, ΔU=500200=300  J\Delta U = 500 - 200 = 300 \ \text{ J}.
    3. Answer: The entropy of the system must increase (ΔS>0\Delta S > 0).
      The Second Law states that for any spontaneous process, the total entropy of the universe increases. For an isolated system, this means the entropy of the system itself must increase.
    4. Answer: 1,155  J1,155 \ \text{ J}.
      Use the calorimetry formula q=mcΔTq = mc\Delta T. q=(50.0  g) ×(0.385  J/g C) ×(8020 C)=50 ×0.385 ×60=1,155  Jq = (50.0 \ \text{ g}) \ \times (0.385 \ \text{ J/g} \cdot ^{\circ}\ \text{C}) \ \times (80 - 20 ^{\circ}\ \text{C}) = 50 \ \times 0.385 \ \times 60 = 1,155 \ \text{ J}.
    5. Answer: Enthalpy (HH).
      Enthalpy is defined as H=U+PVH = U + PV. At constant pressure, the change in enthalpy (ΔH\Delta H) is equal to the heat exchanged (qpq_p).
    6. Answer: ΔS<0\Delta S < 0 (Negative).
      The reaction starts with 4 moles of gas (1 N2N_2 + 3 H2H_2) and produces 2 moles of gas (2 NH3NH_3). A decrease in the number of gas moles results in a decrease in disorder, hence negative entropy.
    7. Answer: ΔG<0\Delta G^{\circ} < 0 (Negative).
      The relationship is ΔG=RTlnK\Delta G^{\circ} = -RT \ln K_{ \neq}. If K>1K_{ \neq} > 1, then lnK\ln K_{ \neq} is positive, making ΔG\Delta G^{\circ} negative. This is a common theme in Medium MCAT Equilibrium Practice Questions.
    8. Answer: The gas has higher entropy.
      Gases have much more translational freedom and occupy a larger volume than liquids, leading to more microstates and higher disorder (entropy).
    9. Answer: The temperature decreases.
      In an adiabatic process, Q=0Q = 0. Therefore, ΔU=W\Delta U = -W. If the system does work (W>0W > 0), the internal energy (ΔU\Delta U) must decrease. Since internal energy is proportional to temperature, the temperature drops.
    10. Answer: 100  kJ-100 \ \text{ kJ}.
      Simply sum the enthalpy changes of the steps: (120)+50+(30)=100  kJ(-120) + 50 + (-30) = -100 \ \text{ kJ}.
    Interactive quizQuestion 1 of 5

    1. Which of the following conditions always results in a spontaneous reaction?

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    Frequently Asked Questions

    What is the difference between ΔG and ΔG°?

    ΔG\Delta G represents the free energy change under any specific set of conditions, while ΔG\Delta G^{\circ} is the free energy change under standard conditions (1 M concentration, 1 atm pressure, and 298 K). They are related by the equation ΔG=ΔG+RTlnQ\Delta G = \Delta G^{\circ} + RT \ln Q.

    Can a reaction with positive ΔH be spontaneous?

    Yes, an endothermic reaction can be spontaneous if the entropy change (ΔS\Delta S) is positive and the temperature is high enough such that the TΔST\Delta S term exceeds the ΔH\Delta H term. This makes the overall Gibbs free energy negative.

    What does a negative work value mean in thermodynamics?

    In the convention ΔU=QW\Delta U = Q - W, a negative work value (W<0W < 0) indicates that work is being done on the system by the surroundings, such as during the compression of a gas. This increases the internal energy of the system.

    Why is entropy often called the "arrow of time"?

    Entropy is called the arrow of time because the Second Law of Thermodynamics dictates that the total entropy of the universe must increase over time, providing a clear direction for the progression of natural events. This distinguishes the future from the past in physical processes.

    How do catalysts affect thermodynamic variables like ΔG?

    Catalysts do not affect thermodynamic variables such as ΔG\Delta G, ΔH\Delta H, or ΔS\Delta S because these are state functions that depend only on the initial and final states. Catalysts only lower the activation energy to increase the reaction rate (kinetics).

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    Reviewed by

    Michael Danquah, MS, PhD

    Dr. Michael Danquah is a professor of pharmaceutical sciences and founder of several educational technology platforms focused on improving student learning and performance.

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