What are some common mistakes students make in thermochemistry?

1 Answer
Mar 2, 2016

Off the top of my head, here are some spots for confusion:

  • Recalling that #"E"^@""_ "cell" = "E"^@""_ "red"+"E"^@""_ "ox"#, but that the potential values are typically given only as reduction potentials, so the oxidation potentials are the version with the opposite sign.
  • The oxidation reactions are also the reverse (flipped reactants or products) of the reduction reactions typically provided.
  • Cell potentials for a galvanic cell should always be positive -- set up reduction and oxidation potentials to achieve the greatest cell potential possible.
  • In a galvanic cell, oxidation occurs at the anode and reduction at the anode.
  • Electrons flow from the anode to the cathode.
  • Anions from the salt bridge flow to the anode, and cations flow towards the cathode.
  • When balancing half-reactions, pay attention to acidic or basic surroundings and add #"H"^+#, #"OH"^-#, and/or #"H"_2"O""# accordingly.
  • Balance electrons in the half reactions -- the number of electrons when balanced is the number of electrons used in equations like #Delta"G"^@=-n"FE"^@#.
  • To move from #"C"# to #"mol e"^-#, divide by Faraday's constant. To go the other way, from moles to coulombs, multiply by #96485#.
  • When calculating Gibbs free energy, not realizing that enthalpy is often given in #"kJ mol"^-1# whereas entropy is commonly given in #"J mol"^-1# #"K"^-1#, so the enthalpy must often be multiplied by #1000# when using #Delta"G"^@=Delta"H"^@-"T"Delta"S"^@#.