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Entropy

based on notes

TermDefinition
state function a mathematical function that depends only on the initial and final states of the system
energy (equation) ∆E = Ef - Ei
∆E change in energy of the system
Ef final energy of the system
Ei initial energy of the system
enthalpy (equation) ∆H = Hf - Hi
∆H change in enthalpy of the system
Hf final enthalpy of the system
Hi initial enthalpy of the system
entropy (equation) ∆S = Sf - Si
∆S change in entropy of the system
Sf final entropy of the system
Si initial entropy of the system
Entropy the measure of disorder (dispersal) present in a system, the extent of randomness in a system
the Third Law of Thermodynamics the entropy of a pure crystalline substance at absolute zero is zero; no disorder and no movement means no entropy
the Second Law of Thermodynamics for any spontaneous process, the entropy of the universe will increase; ∆S universe > 0
entropy of a phase change (equation) ∆S phase change (in J/K) = ∆H phase change (in J) / T (in K)
spontaneous change a change that can occur without work being done to bring it about; can occur on its own; is irreversible
nonspontaneous change a change that can only be brought about by doing work
∆S positive entropy of system increased; ∆S > 0; Sf > Si
∆S negative entropy of system decreased; ∆S < 0; Sf < Si
Gibbs Free Energy (equation) ∆G = ∆H - T∆S
∆G change in Gibbs Free Energy of the system
∆G<0 ∆G is negative, reaction is spontaneous
∆G=0 reaction is at equilibrium
∆G>0 ∆G is positive, reaction is nonspontaneous
temperature in Kelvins always positive
∆H>0 ∆H is positive, reaction is endothermic
∆H<0 ∆H is negative, reaction is exothermic
∆S>0 ∆S is positive, entropy is increasing
∆S<0 ∆S is negative, entropy is decreasing
⁻∆H, ⁺∆S reaction is spontaneous at all temperatures
⁻∆H, ⁻∆S reaction is spontaneous only at low temperatures
⁺∆H, ⁺∆S reaction is spontaneous only at high temperatures
⁺∆H, ⁻∆S reaction is nonspontaneous at all temperatures
When ∆G=0 ∆S = ∆H/T
Created by: ccons
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