Introduction to Biochemistry: Thermodynamics Fundamentals

Topics Covered:

  • Thermodynamics

    • Energy

    • Work

    • Entropy

    • Enthalpy

Page 4: Overview of Thermodynamics

The term thermodynamics originates from the Greek words:

  • θέρμη (therme) meaning heat

  • δύναμις (dynamis) meaning power

Thermodynamics is the branch of science that studies the relationship between energy, work, and entropy.

Page 5: Importance and Nature of Energy

  • All living organisms depend on energy, primarily derived from food.

  • Essential functions supported by energy include:

    • Growth and repair

    • Sustaining life processes

  • Energy can exist in different forms and can be transformed from one form to another.

  • Energy transfer is crucial for driving biochemical processes.

Page 6-10: Forms of Energy

Types of Energy:

  • Electric energy

  • Heat energy from chemical reactions

  • Aeolic energy (wind energy)

  • Solar energy

  • Nuclear energy

Example:

  • Hiroshima (Japan, August 6, 1945), highlighting the destructive power of nuclear energy.

Page 13: Definition of Energy

Energy is defined as:

  • Lacking physical form

  • An intrinsic attribute of any substance or biological system

  • The capacity to do work.

  • The greater the energy possessed by an entity, the more capable it is of bringing about change.

Page 14-15: Understanding Energy's Properties

  • A fundamental property of energy is convertibility.

  • Examples of Energy Transformation:

    • Photosynthesis: Light energy is converted into chemical energy in plants.

    • Batteries: Chemical energy is transformed into light energy.

Page 18: Conservation of Energy Principle

  • Conservation of Energy: Energy cannot be created or destroyed; it can only be transformed from one form to another.

  • Examples:

    • Heating water in a kettle using electrical energy without depleting it.

    • Lighting a match transforms stored chemical energy into thermal energy.

Page 19: Forms of Energy

  1. Kinetic Energy (KE)

    • Energy due to motion.

    • The faster an object moves, the more kinetic energy it possesses.

    • Example: A car moving at 70 mph has 3 times more kinetic energy than one moving at 40 mph.

    • KE depends on the mass of the object: KE = rac{1}{2} mv^2 where $m$ is mass and $v$ is velocity.

  2. Potential Energy

    • Energy due to position or state.

    • Gravitational Potential Energy (GPE): Energy due to an object’s position relative to the earth.

    • Transformers into kinetic energy when released.

Page 20: Examples of Energetics

  • Kinetic Energy Explained:

    • A heavy object moving at a specific speed has more KE than a lighter object at the same speed.

  • Gravitational Potential Energy Explained:

    • Used in examples like hydroelectric dams, where stored water has GPE that can be converted to KE as it cascades down.

Page 24: Chemical Potential Energy

  • Energy within atoms bonded by covalent or ionic interactions.

  • Amount of energy needed to overcome these bonds, known as bond energy.

  • Examples of bond energies:

    • C-H bond: 412 kJ/mol

    • N-H bond: 390 kJ/mol

  • Stronger bonds require more energy to break.

Page 25: Scientific Definition of Energy

  • Energy is the capacity to do work.

Page 26: Work Defined

  • Work can be described as any process capable of lifting a weight.
    Example: Lifting a book involves chemical energy converting to kinetic energy to overcome gravitational potential energy (GPE).

Page 27-28: Spontaneous vs. Non-Spontaneous Processes

  • Spontaneous Process:

    • Transfer of energy as heat from high temperature to low temperature without external energy input.

  • Non-Spontaneous Process:

    • Energy transfers from low temperature to high temperature, needing energy input.

Page 29-30: Understanding Entropy

  • Entropy derives from the Greek words indicating a 'turning towards.'

  • It describes the direction and likelihood of spontaneous changes.

  • Entropy has universal applications in thermodynamics.

Page 31-33: Entropy and Spontaneity

  • Entropy increases in spontaneous processes.

  • In spontaneous changes: Disorder increases, and entropy increases.

  • In non-spontaneous changes: Work is required to decrease entropy and achieve order.

Key Note: Non-spontaneous processes do not imply impossibility.

Page 37: Measuring Entropy

  • Entropy measures the distribution and dispersion of energy within a system.

  • Higher entropy indicates wider energy distribution and increased disorder.

Page 38: Reversing Entropy

  • Reversing entropy involves high-information work, often vital in biological systems.
    Quote by Gilbert Newton Lewis: “Gain in entropy always means loss of information.”

Page 39: Energy Changes in Chemical Reactions

  • In chemical reactions, energy can be absorbed or released.

  • This is characterized as enthalpy change (ΔH), which encapsulates the energy changes associated with bond formation and breaking in reactions.

Page 40-44: Enthalpy Explained

  • Positive Enthalpy (Endothermic Reaction):

    • More energy is required to break original bonds than is released when forming new ones.

    • Energy is absorbed from the surroundings, indicating that heat input is required.

  • Negative Enthalpy (Exothermic Reaction):

    • More energy is released upon bond formation than is absorbed for bond breaking.

    • Energy is released into the surroundings, indicating that the reaction can proceed easily without added energy.

-Heat is considered a degenerate form of energy due to its inefficiency in producing work and its high entropy.

Page 45: Gibbs Free Energy (ΔG)

  • Gibbs Free Energy quantifies the interplay between entropy and enthalpy.

  • Formula:
    riangle G = riangle H - T riangle S

Where:

  • ( riangle G) is Gibbs free-energy change (kJ/mol)

  • ( riangle H) is the change in enthalpy (kJ/mol)

  • (T) is temperature (Kelvin)

  • ( riangle S) is the change in entropy (J/K·mol)

Page 46-47: Biological Applications of Gibbs Free Energy

  • In biological contexts, energy from spontaneous reactions (negative ΔG) can drive non-spontaneous (positive ΔG) reactions.

  • Cellular Respiration: A process where glucose (C₆H₁₂O₆) is consumed, releasing energy in a controlled manner through multiple reactions to yield ATP.

  • Example reaction for aerobic cellular respiration:
    C₆H₁₂O₆ + 6O₂
    ightarrow 6CO₂ + 6H₂O ext{ (ΔG = -2879 kJ/mol)}

  • The energetics of metabolic processes involve coupling catabolic (energy-releasing) and anabolic (energy-consuming) reactions, thereby balancing cellular metabolism.

Page 48: Conclusion and Questions

  • The lecture concludes with a reflection on thermodynamic principles and their importance in biological systems.

  • Questions: Encouragement for students to engage and clarify concepts discussed during the lecture.