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Heat (q)
energy transferred between objects due to a temperature difference; flows hot → cold.
Temperature
average kinetic energy of the particles in a substance.
System / surroundings
the system is the reaction being studied; the surroundings are everything else.
Exothermic
process that releases heat; q and ΔH are negative.
Endothermic
process that absorbs heat; q and ΔH are positive.
First Law of Thermodynamics
energy is conserved; ΔE = q + w.
Specific heat (c)
energy needed to raise 1 g of a substance by 1 °C; water = 4.18 J/(g·°C).
Calorimetry
measuring heat flow, based on heat lost = heat gained (q = mcΔT).
Enthalpy (ΔH)
heat content of a system at constant pressure; ΔH = H_products − H_reactants.
Bond enthalpy
energy to break a bond; ΔH ≈ (bonds broken) − (bonds formed).
Hess's Law
ΔH of an overall reaction equals the sum of the ΔH of its steps (enthalpy is a state function).
Standard enthalpy of formation (ΔH°f)
heat to form 1 mol of a compound from its elements in standard states; = 0 for a pure element.
State function
a property that depends only on the current state, not the path taken (e.g., H, S, G).
Entropy (S)
measure of the dispersal of energy and matter; increases with gases, dissolving, and higher temperature.
Gibbs free energy (ΔG)
predicts spontaneity; ΔG = ΔH − TΔS. Negative ΔG = spontaneous.
Spontaneous (thermodynamically favored)
a reaction that proceeds forward on its own (ΔG < 0); note this says nothing about speed.