Firstly, on the issue of reversible reactions in dynamic equilibrium, e.g. N2+3H2 -> 2NH3. When pressure increases, I'm confused as to what happens.
1) Rate of forward reaction increases temporarily to shift equilibrium to right, after which the rate of forward and backward reaction return to the same, hence the yield of NH3 increases (Then what should the option be in multiple choice between rate of forward increases and stays the same, since it increases only temporarily but stays the same afterwards)
2) But by rate constant k = Aexp(-Ea/RT), the rate of reactions should only depend on activation energy, temperature and orientation of molecules, so rate of forward and backward reaction should not be affected by pressure.
3) But then again, by kinetic model of matter, when pressure increases, the molecules will collide with each other more frequently, so rate of both forward and backward reaction will increase.
Some of these contradict each other, so I'm not so sure which one is correct.
Secondly, on the issue of thermal stability of metal compounds. One theory is where the metal cation distorts the electron cloud of the polyatomic anion, hence making it less thermally stable. As positive charge density of the metal cation increases, distortion of electron cloud increases and hence thermal stability decreases. However, I'd like to make a contrast to lattice enthalpy, where the lattice enthalpy is inversely proportional to the size of the cation and directly proportional to its charge, hence as charge density increases, electrostatic forces of attraction should increase, so shouldn't it require more heat energy to decompose?
Thirdly, if Ag is so large and its charge is only +1, it should have a small positive charge density and so it should not distort the electron cloud of the large anion. So, why is its compound, e.g. AgCO3, so unstable?
Fourthly, taking a voltaic cell where the electrolyte is pure water, will any current flow? A multiple choice question said zero current will flow through as water is a simple molecule, but shouldn't there be sufficient H+ and OH- ions to conduct electricity due to auto-ionisation of water?
Fifthly, considering another voltaic cell where the anode is Copper, and the electrolyte contains cations A+, then when oxidation occurs at Cu anode, Cu 2+ ions are liberated into the electrolyte. The A+ should then be reduced at the cathode to become A. But what if Copper is less reactive than A, meaning that the Cu2+ ions that were liberated are more likely to be reduced than A+ instead? Will Cu2+ be reduced instead, or do we have to consider concentrations of each cation? Assuming we do, then after a significant period of time, as more Cu2+ ions are produced and more A+ becomes A, then will Cu2+ start to be deposited as Cu instead? So the cathode will first have a layer of A, then Cu. o.0
Sixthly, in what event is NO3- reduced to NO and NO2, and in what event is it reduced to NH3 instead? I am aware that H2 can act as a reducing agent to reduce NO3- to NH3 in the test for nitrates in unknown solutions, but I was confused when I read elsewhere that it can be reduced to NO and NO2.
Seventhly, in a voltaic cell, a voltmeter is usually added as a component to the external circuit, connected to the wires, to measure the electrode potential. However, doesn't this contradict with the physics concept where voltmeters should be connected in parallel instead? If they are connected in series, wouldn't their extremely high resistance affect the results?