Page 49 - A Working Method Approach For Introductory Physical Chemistry Calculations
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Thermodynamics II                                         33

       WORKING METHOD FOR THE CALCULATION OF AG TYPE
                               PROBLEMS
       A common  problem  on examination  papers is, when  given  a  set of
       AH" and  So data,  you  are asked to evaluate  AGR,.  The following
       working method  describes a skeleton step-by-step outline on how to
       approach such a problem.

          1. Read the question carefully.
          2.  Identify  the  species involved (the reactants  and  the  products)
             and identify their states, i.e. (*) = (s), (1) or (g).
          3.  Write  down  a  balanced  chemical  equation,  with  the  states
             indicated,  i.e.  vAA(+) + VBB(+) --+  v&+)  + nDD(*), where  VA,
             vB, vc and vD, are the stoichiometry factors.
          4.  Determine  AH;xn  =  [( vc  x  AH;(,,)  + (VD x  AH;(,,,)]   -
             [(VA xAH;(A)) + (vg x AH&,))],  i.e. AH&, = C[AH;(Products)]
             - C[AH;(Reactants)]. Remember AH;(element)  = 0, and do
             not forget the units.
          5. Determine ASK,,  in a similar fashion: ASR,  = C[S"(Products)]
             - C[S"(Reactants)], but  S"(e1ement) is not  equal  to O!  Write
             down the units of AS".
          6. Determine  the  temperature,  T  in  K.  Remember  T(K) =
             [T("C) + 2731 K.
          7.  Convert AH" and AS" to the same system of units, i.e. AH" in
             J mol-'  and AS" in J K-'  mol-'  or AH" in kJ mol-'  and AS"
             in kJ K-* mol-'.
          8. Determine  the  value  of  AGO,   using  the  equation
             AGO  = AH" - TAS", i.e. 'Gibbs HaTS'!
          9. Answer  any  riders  to  the  question.  For  example: AH"  -ve,
             exothermic reaction; AH" + ve, endothermic reaction; AS" - ve,
             decrease in the entropy or the disorder of the reaction; AS' + ve,
             increase in the entropy or the disorder of the reaction; AGO  - ve,
             spontaneous  reaction;  AGO  + ve,  non-spontaneous  reaction;
             AG  = 0 reaction at equilibrium (explained in Chapter 4), where
             K is defined as the equilibrium constant.
          10. At equilibrium,

             1  AG = AGO + RTlnK= 0 I  + 1nK = -AG"/(RT).
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