Help me understand. Determine the equilibrium constant for the following reaction at 398 K. 3Cu(s) + 2MnO4- (aq) + 8H+(aq) --> 3Cu2+(aq) + 2MnO2(s) + 4H2O (l)
hm have you used the nernst equation?
yes we have before but the instructor, she goes thru it so fast in her slides that I can hardly keep up an we have an exam on tuesday @aaronq
@aaronq its that E cell = ECell standard potential -.0592V/n logQ
at equilibrium \((i.e.~E_{cell}=E^o_{cell})\), so you can solve for K. \(0=E^o_{cell}-\dfrac{RT}{nF}lnK\rightarrow E^o_{cell}=\dfrac{RT}{nF}lnK\rightarrow lnK=\dfrac{nFE^0_{cell}}{RT}\)
wha?! haha but do i have k?
K is the equilibrium constant (what you're looking for).
remember that the reduced equation you wrote can only be used at 298 K, 1M concentration and at 1 atm (i.e. standard conditions) which is not the case here (398 K).
oh...okay haha so what do I do?
@aaronq im looking at my note paper with equtions there is a Ecell=.0592V/n * log K and there is a Ecell = Ecell- .0592V/n *logQ
use the original form: \(E_{cell}=E^0_{cell}-\dfrac{RT}{nF}lnK\) , which solves to what i wrote above
okay. so then... here hold on .. the nF = hold on I have to do that reduction oxidation thingy right? and for that oxidation would be anode so negative, an cathode is reduction that is positive right? Im just making sure I have this part right first. @aaronq
I also found this chart just in case http://bilbo.chm.uri.edu/CHM112/tables/redpottable.htm
UGH!!! IM SO LOST! okay this is what I understand from your formula: nF= the number of mol electrons R= the constant, i think its 8.314 J/mol K T= is the temperature=398K @aaronq Is all of this right so far? okay I just dont remember how to find the \[E^0 cell\]
n = # of electrons exchanged in redox reaction: 3Cu(s) + 2MnO4- (aq) + 8H+(aq) --> 3Cu2+(aq) + 2MnO2(s) + 4H2O (l) 6 electrons
F = faradays constant
okay F = Faradays constant is 96485 C/mol e-
yep, thats right. now you just need to find the potential of the cell \(E^0_{cell}=E^{red}_{cathode}-E^{red}_{anode}\)
sometimes it's also written as \(E^0_{cell}=E^{red}_{cathode}+E^{oxd}_{anode}\)
oh....okay wait haha i always thought u would subtract it, but I guess I keep getting it wrong, so basically it becomes an addition
you subtract it if both of your values are reduction potentials. you add them if one is oxidation (at anode) and one is reduction potential (at cathode).
okay so @aaronq the anode would be the positive charge right? or am i mixed up. I remember An-Ox for Anode=Oxidation= - and Red-Cat for Cathode=Reduction=+
\(\huge \color{red}OI\color{red}L ~~\color{blue}RI\color{blue}G\) Oxidation loss of electrons (at anode) Reduction gain of electrons (at cathode)
okay let me see if I have this right then
SORRY @aaronq INTERNET CONNECTION IS being lame
no worries !
okay the Cathode, or reduction reaction is going to be the 2MnO4
yes
right? cuz it goes from a 2MnO4- to a 2MnO2; it ganed the e- to make it a positive and added Oxygen :D
ok, so then now that i know that
okay E cell.er....um..... okay hold on
sorry, i read that as "now what" lol
Would I use....half reactions for the Ecell(V) ?
yes
so find these reactions in a reduction potential chart and set them up
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch20/electro.php Im using this website
Cu2+ + e- <-----> Cu+ 0.158 so I would flip it right? and MnO4- + 2 H2O + 3 e- <-----> MnO2 + 4 OH- 0.588
@aaronq
you're using this one Cu2+ + 2 e- <-----> Cu 0.3402
but yeah flip that one
wait haha I just forgot, but why do I flip it?
and why do I use that one an not the others? @aaronq
@aaronq I also cant figure out which MnO4 to use: MnO4- + 2 H2O + 3 e- <-----> MnO2 + 4 OH- 0.588 or MnO2 + 4 H+ + 2 e- <-----> Mn2+ + 2 H2O 1.208 or MnO4- + 8 H+ + 5 e- <-----> Mn2+ + 4 H2O 1.491
well in the main equation they have an 8H+ --> 4H+ would I use the bottom one that gives me 1.491? @aaronq
you flip it if you're adding the values together, because as it's written it is a reduction equation and you're looking for the oxidation.
i would use the top one from those 3
ohh...okay haha @aaronq thank you so then is this right, okay dang hold on gotta do it again but not use the bottom number
no i mean the bottom one. use the bottom one of the 3
OKAY, oh........haha okay let me do it again hold on haha
okay @aaronq I did the Ecell= C+A 1.491+-.34 = 1.151v
right?
right?
yep thats right
@aaronq sorry I keep loosing connection, is ur computer the same way?
no, i was just away from the computer. so, \(\huge K=e^{\small(\dfrac{nFE^o_{cell}}{RT})}\)
OH! ahah u rearranged that one equation huh? haha
haha yeah, you should try it yourself on paper to make sure you can arrive at the same result
@aaronq Im going to need your help big time right now because. I dont remember the n, you said the n was the number of elections exchanged in redox reaction. u said that was 6 because there was 3 Cu and 2MnO4's so you times them and got 6 right?
yes
okay then so.. @aaronq
e=1.151v
\[1.151v (\frac{ 8.314*398K }{ 6*96485 })lnK\]
oops I think I did it wrong @aaronq
\[k=1.151v(\frac{ 6*96485*e^0cell }{ 8.314*398K })\] Right ????@aaronq
@aaronq is the answer....Well I dont know what to put for the e^0 Cell :/
this dumb connection! @aaronq
so you had to end up with: \(\sf K=e^\dfrac{6*(9.65*10^4 C/mol)*1.151V}{(8.314 J/mol*K)*(398K)}\)
im back @aaronq
yes I did @aaronq but what do i put for the e??
@aaronq I get K=e 201.4
do i use that 10^?? to get.... WOW, haha I got an over flow error
"e" is euler's number. it's transcendental but you can write it as 2.718 so it's \(2.718^{2.93*10^{87}}\) i'm getting \(\infty\), which just means that the number is too big for my calculator lol
okay @aaronq i got a big number haha. I dont even think we were doing that part right. Here is what I am given on an equation sheet of mine
I will be back online in the morning.
i think it was late and i was doing something wrong. now ii'm getting \(e^{201.4}=2.93*10^{87}\) which seems right.
ps i'm 100% sure were using the right equation.
haha @aaronq okay Im back! had to go out to store.
@aaronq but where okay hold on so this was the equation we were working on: well this part: \[K=e(\frac{ 6*96485*1.151v }{ 8.314*398K })\] giving us: \[K=e(\frac{ 666325.4 }{ 8.314*398K }) \] \[K=e201.4\] @aaronq NOW, do we raise both to the e^, but how does it get rid of the K? I understand how u got\[K=e^{201.4} = 2.93x10^{87}\]
when you have: \(lnK=\dfrac{nFE}{RT}\) you have to raise both sides to the \(e^x\) to get rid of ln. so you end up with \(\Huge K=e^{\small \frac{nFE}{RT}}\) e^(nFE/RT)
oh. okay that makes sense now lol sorry
the formatting its kinda weird because there are so many symbols in the exponent, which makes like it look like a multiplication, but it's not.
no problem ! hope everything is good now
okay so now that we have the K=2.93x10^87 that will be our volts, right?
no that's the equilibrium constant (usually unitless)
really? so we just solved it? I thought there would need another equation
hah yep thats it
Dang....Longest problem ever
thank you so much. I have other problems too that I will post on here in a little bit.
no problem !
Join our real-time social learning platform and learn together with your friends!