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Chem test 3

QuestionAnswer
Change in entropy equation ΔS=ΔSf-ΔSi/ /ΔS=qrev/T (constant T)
Change in entropy of surrounding equation ΔSsurr=(-ΔHsys)/T (constant P and T)
Enthalpy change ΔH
Entropy change ΔS
Entropy equation S=(k)ln(W)
Work equation wf/wi
qrev equation qrev=nxΔHvap
Change in entropy of universe equation ΔSuni=ΔSsys+ΔSsurro (must be +)
qsurr=-qsys -
Boltzmann contant k=1.38x10^-23
Change in entropy of system equation ΔS*rxn= ∑[np(S*{products}]- ∑[nr(S*{reactants}]
Change in Gibbs free energy equation ΔG=ΔHsys-T(ΔSsys)
Gibbs free energy spontaneous ΔG<0
Gibbs free energy nonspontaneous ΔG>0
Gibbs free energy equilibrium ΔG=0
Change in Gibbs free energy of reaction (equation 2) (@25 *C) ΔG*rxn= ∑[n(ΔG*f{products}]- ∑[n(ΔG*f{reactants}]
Total change in Gibbs free energy ΔG*tot.=ΔG*react1+ΔG*react2+...
Equilibrium constant equation (K) aA+bB <-> cC+dD (only aqueous solutions and gases) K= [C]^c[D]^d/[A]^a[B]^b
Reverse reaction is favored. More reactants than products K<<1
Forward reaction is favored. More products than reactants K>>1
Nether direction is favored. K=1
Reaction quotient (Qc) Using K equation with the initial concentrations
System goes from left to right to reach equil. Qc<Kc
System goes from right to left to reach equil. Qc>Kc
System @ equil. Qc=Kc
ΔG under nonstandard conditions ΔG=ΔG*+(R)(T)lnQ T= in K
R value for J/K R=8.314 J/K
ΔHrxn equation ΔHrxn=∑products(npΔHf)−∑reactants(nrΔHf)
When ΔH is negative and ΔS is positive ΔG is negative at all temperatures
When ΔH is positive and ΔS is negative ΔG is positive at all temperatures.
When both ΔH and ΔS are negative ΔG will be negative at low temperatures and positive at high temperatures
When both ΔH and ΔS are positive ΔG will be negative at high temperatures and positive at low temperatures.
Created by: mandi239
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