Life'sHard
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- 2025
Ohhh I see I didn't even relate the volume increase with c=n/v. Tyvm.1) It's a Le Chatelier's Principle question as there is like an equilibrium. More solvent in the X part means concentration of I2(x) decreases as in c=n/v the volume has gone up. This means the equil. is disturbed and shifts right to minimise change. Leading to increase in I2(x) and decrease I2(Y). So B. C and D, dont make sense for this as temperature changing is what changes the K value
3[Ba2+] = [OH-] (as there's 3 times as much of OH-)2) Whenever questions have things about concentrations or values in general, it is a good idea to write some formulas or equations. Here there is dissolving equations:
Ba(OH)2(s) --> Ba2+(aq) + 2OH-(aq)
NaOH(s) --> Na+(aq) + OH-(aq)
So in total we have 1Ba2+, 1Na+ and 3OH-
[Ba2+] = [Na+]
3[Ba2+] = [OH-] (as there's 3 times as much of OH-)
If [Na+] = [Ba2+], then arrange that above eqn a little to:
[Ba2+] + 2[Ba2+] = [OH-]
and sub the [Na+] = [Ba2+]
[Na+] + 2[Ba2+] = [OH-]
Another perspective:
Thank you so much that made a lot more senseIt's like doing a molar ratio like you would with a normal equation.
The equation for polymer formation is:
5 galic acid ---> tannic acid + 4H2O
so from part (a) if it is known: n(gallic acid) = 0.0001092 mol
n(tannic acid) = 1/5 n(gallic acid)
using a molar ratio for that equation
Thanks man. Really appreciate your activity in these forums. You've really helped!Esterification is an equilibrium phenomenon, and so does not go to completion.
Do a mole calculation on the reaction
methanol + ethanoic acid ---> methyl ethanoate + water
where methyl ethanoate is CH3COOCH3. Work out the theoretical yield of the ester based on the whichever of the two reagants is limiting, then find 24% of that.
As for additions, hydrogenation definitely needs a catalyst. Hydration and hydrohalogenation are acid catalysed, though in the case of hydrohalogenation the catalyst comes from the HX itself and the reaction will certainly occur in gas phases. Halogenation of an alkene does not require a catalyst though substitution side reactions are possible if there is UV light around. I would call it a fairly rapid addition and the only product will be 1,2-dichloroethane.