thermodynamics Flashcards

look at thermodynamics - pressure and temperature

1
Q

Thermodynamics Basics

A

Definition: Thermodynamics is the study of energy and transformations.
Focus: Concerned with macroscopic properties (temperature, volume) and equilibrium conditions.
Limitations: Does not deal with the speed of reactions.

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2
Q

Thermodynamics Predictions

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Prediction Nature: Predicts equilibrium states, favors the side with the lowest energy.
Example: Diamonds are stable on Earth’s surface, but they may be physically abraded before chemically degrading to graphite (thermodynamics favors graphite).
Equilibrium Misconception: No measurable change doesn’t guarantee equilibrium; further change may still occur.

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3
Q

Fundamental Thermodynamic Variables

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Energy: Capacity to produce change; changes in energy are more critical than absolute energy.
Forms of Energy: Includes work and heat; heat results from random motion of molecules, related to kinetic energy.
Units: Energy in Joules (J), force in Newtons (N), distance in meters (m), time in seconds (s), mass in kilograms (kg), temperature in Kelvin (K), pressure in Pascals (Pa).

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4
Q

work energy

A

Work Definition: Done by moving a mass (M) through a distance (x) against a force (F): w = Fx
w=F⋅x.
Units: Joules (J) = Newtons (N) × meters (m).
Force Definition:
F = m a
F=ma, where
a is the acceleration due to gravity on Earth (approximately 9.8 m/s²).
Example: 1 kg at rest exerts a force of 9.8 N on Earth’s surface.

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5
Q

Thermodynamics and equilibrium

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Nature of Prediction: Thermodynamics predicts the equilibrium state; reaching equilibrium may take timescales we can’t measure.
Diamond Stability Example: Diamonds are so stable on Earth’s surface that physical abrasion may occur before chemical degradation to graphite.
Physical Example: Releasing a boulder from the top of a slope - most stable at valley floor, but a hollow on the valley wall may prevent reaching the lowest energy state.

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6
Q

thermodynamics variables

A

Entropy (S): Measures the degree of randomness in a system (J mol⁻¹ K⁻¹).
Enthalpy (H): Measures heat exchanged in a reaction (J mol⁻¹ or kJ mol⁻¹).
Free Energy (G): Measures total energy (enthalpy + entropy) in a reaction (J mol⁻¹ or kJ mol⁻¹).

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7
Q

system change and equilibrium

A

System Change Requirement: Energy change is essential for a system to change.
Equilibrium Significance: No energy change; system is at equilibrium.
Example: Saturated sodium chloride solution where additional salt doesn’t dissolve but remains as a pile.

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8
Q

types of equilibrium

A

Spontaneous Reaction: Energy change from high to low, losing energy to the system.
Equilibrium: No exchange of energy.
Dynamic Equilibrium: No thermodynamic or chemical composition change, but can exchange matter.
Static Equilibrium: No change in composition or matter exchange at observable timescales.

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9
Q

calculating Delta H

A

Delta H Formula:
ΔH = H products − H reactants
Exothermic Reaction: ΔH negative, heat given off; often spontaneous.
Endothermic Reaction: ΔH positive, heat taken in; system feels cold (e.g., evaporation).

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10
Q

Mole and Gibbs Free Energy

A

Mole Definition: One mole =
6.022 × 10^23 molecules or atoms.

Atomic Weights: Average atomic mass relative to 12C
Gibbs Free Energy: G=H−TS, where ΔG=ΔH−TΔS.
Equilibrium: Gibbs free energies of products and reactants are equal.
Spontaneity: Reaction is spontaneous when ΔG is negative.

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11
Q

temperature conversion to kelvin

A

add 273

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12
Q

Stoichiometry

A

refers to the realive molar amounts of species in a reaction

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13
Q
A
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