ATAR Notes: Forum
VCE Stuff => VCE Science => VCE Mathematics/Science/Technology => VCE Subjects + Help => VCE Chemistry => Topic started by: /0 on November 11, 2009, 03:37:32 pm
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Alright yall let's make a thread of STUFF WE GOTSTA KNOW
GOGOGOGOGOGOGOGO!!!
Here's some stuff to kick us off:
Nuclear Fusion

Energy stored in plants:
+6H_2O(l) \rightarrow C_6H_{12}O_6(aq)+6O_2(g))
Combustion of coal in a power station
+O_2(g) \rightarrow CO_2(g))
Oxidation of sulfur impurities in the coal
+O_2(g) \rightarrow SO_2(g))
(courtesy Kilbaha '09)
- Catalysts speed up reactions by providing an alternative pathway of lower activation energy. Reactants adsorb to the surface of catalysts where they meet and react. Catalysts do not affect equilibrium yield.
- Only temperature can affect the equilibrium constant!
- The conditions for the electrochemical series are 1M, 25 degrees celcius, and 1 atm (e.g. Brine > 1M, so Cl(g)/Cl- drops below the water reaction)
ENDOTHERMIC 
- You can only recharge cells if the products of the discharging reaction do not leave the surface of the electrodes
- If you are electrolysing a solution containing Cl- ions, even though Cl(g)/Cl- is higher than the water reaction, thre is chance that Cl(g) will be given off if the voltage is high enough.
- In a secondary cell, no matter whether you're charging or discharging, the negative electrode stays negative, and the positive electrode stays positive. However, anode and cathode swap.
- If asked to derive
, find })
- If asked to derive
, find
where X is anything. Do not use Faraday's constant, it is itself derived from 
- If you dilute a strong acid its pH will change more than for a weak acid. This is due to it already being fully ionised. The weak acid will ionise more if you dilute, due to LCP.
- If you need to draw a half-cell and one of the reactants is a gas, you need to draw a gas electrode (there's a pic in your heinemann textbook)
- In oxygen-hydrogen fuel cells, electrodes must be catalytic and porous. In general they must also be inert and conducting.
- You must use Brine in a membrane cell (producing Sodium hydroxide). It is concentrated NaCl, which allows the Cl(g)/Cl- reaction to go below the water reaction on the electrochemical series.
- The Down Cell (producing Sodium) must use molten NaCl
- You must use Cryolite in a Hall-Heroult Cell (producing aluminium) (you don't need to remember the formula of cryolite), in order to lower the temperature required for the reaction.
- The electrochemical series cannot predict the rate of reaction. Don't even try it.
- In a galvanic cell the ions in the salt bridge must be soluble, but also inert.
- Inert electrodes include Graphite and Platinum, with the former being more expensive but also having some catalytic properties.
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It can be negative!
- An equation
does not imply that the concentration graphs will start with
NO! The equilibrium constant must always be obeyed! To differentiate between species on a graph when they have not been labelled, refer to next dot point
- In
, any changes driven by LCP will involve the graphs increasing/decreasing in ratio 1:2:1 for A:B:C
respectively. i.e. the number in front of the chemical will govern how much the graph of that chemical increases/decreases due to LCP.
- Faraday's Laws
1.
(m is mass deposited)
2. In order to produce 1 mole of metal, a whole number of mole of electrons must be consumed.
- Biochemical Fuels
Fermentation of glucose to ethanol:
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Alright yall let's make a thread of STUFF WE GOTSTA KNOW
GOGOGOGOGOGOGOGO!!!
Here's some stuff to kick us off:
Nuclear Fusion

Energy stored in plants:
+6H_2O(l) \rightarrow C_6H_{12}O_6(aq)+6O_2(g))
Combustion of coal in a power station
+O_2(g) \rightarrow CO_2(g))
Oxidation of sulfur impurities in the coal
+O_2(g) \rightarrow SO_2(g))
(courtesy Kilbaha '09)
- Catalysts speed up reactions by providing an alternative pathway of lower activation energy. Reactants adsorb to the surface of catalysts where they meet and react. Catalysts do not affect equilibrium yield.
- Only temperature can affect the equilibrium constant!
Just remember the velocity of a reaction (courtesy kilbaha)
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Are you kidding? Do we actually have to know about nuclear fusion in the sun?!
Oh, also fun fact of the day - did you know nuclear fission is endothermic in the sun between elements from hydrogen to iron :)
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Oh, also fun fact of the day - did you know nuclear fission is endothermic in the sun between elements from hydrogen to iron :)
Why u say between those elements its endothermic, theyre the only elements the sun can consist of, nothing heavier exists within a sun.
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LCP is
PARTIAL
offset only.
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LCP is PARTIAL
offset only.
what do you mean by offset??
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LCP is PARTIAL
offset only.
what do you mean by offset??
Yeh
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LCP is PARTIAL
offset only.
what do you mean by offset??
Yeh
hmmm... that doesn't really answer the question..
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LCP is PARTIAL
offset only.
what do you mean by offset??
Yeh
hmmm... that doesn't really answer the question..
If a change occurs in a reaction to increase the pressure, say decreasing volume, lcp will partially offset with increase in pressure. That is to say there is still an overall net decrease in pressure in the end.
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Activation energy is always positive, as, for a chemical reaction to proceed, additional energy is required to break bonds in reactant particles. Additional energy means it must be positive.
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Nuclear fusion reaction was only in previous study design
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Nuclear fusion reaction was only in previous study design
but it appeared in kilbaha and that makes us worry i guess
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any1 feel like teaching me unit 4 in 16 hours 53 minutes?
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any1 feel like teaching me unit 4 in 16 hours 53 minutes?
So you get one oxidant and a reductant and they make the good stuff
but itll only work if they are good together^^
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- In a secondary cell, no matter whether you're charging or discharging, the negative electrode stays negative, and the positive electrode stays positive. However, anode and cathode swap.
Could you re-word that/explain again :S
- If asked to derive
, find
where X is anything. Do not use Faraday's constant, it is itself derived from 
Do you happen to remember an exam from 08-09 that has a question involving finding Faraday's constant? I know there's one but otherwise I'll just go searching through each slowly..
And to add to this thread: Don't forget that
cannot magically appear as a reactant in half equations :)
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Oh ok, when a secondary cell is discharging,
___(V)__
| |
| |
\_/ \_/
Just say the right electrode is negative. It will be the anode. Then the left will be positive and cathode.
___+Battery-__
| |
| |
\_/ \_/
Now when charging, the right electrode is still negative, but now it's the cathode.
The left electrode is still positive but it's the anode.
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I think the fusion in the sun only appeared in the Kilbaha exam and Kilbaha is sometimes a bit.. "eh".
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Oh, also fun fact of the day - did you know nuclear fission is endothermic in the sun between elements from hydrogen to iron :)
Why u say between those elements its endothermic, theyre the only elements the sun can consist of, nothing heavier exists within a sun.
False. In a dying star, lots of things can happen. (Stars are universal element factories, they convert hydrogen to helium to lithium and keep going until Iron, in their healthy lifespan. Just before they completely die, they spit out the heavier more exotic elements such as lead, uranium, etc, basically everything in the periodic table).
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Efficiency-style questions:
(Let's suppose a percent, 75% OK?)
If the number required is larger than the answer you worked out (because you've only got 75% product from a particular process and you need to work out the amount of reactant, for example) then you multiply it by 100/75
But if the number is smaller than what you worked out (for example, because the process is 75% efficient), then multiply it by 75/100!
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Lol at the efficieny-style question :P
Thanks /0 for the diagrams, the original wording kinda confused me (probably 'cuz of my downtime or something)
Question about the star thing, why does it stop at Iron? irrelevant to the upcoming exam I know, but it sounds interesting :)
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Lol at the efficieny-style question :P
Thanks /0 for the diagrams, the original wording kinda confused me (probably 'cuz of my downtime or something)
Question about the star thing, why does it stop at Iron? irrelevant to the upcoming exam I know, but it sounds interesting :)
I don't remember :(
And yeah, positive reinforcement for the efficiency questions :)
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Iron is one of the most stable elements because it has a high binding energy, which means it is hard to pull it apart:
http://en.wikipedia.org/wiki/File:Binding_energy_curve_-_common_isotopes.svg
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Efficiency-style questions:
(Let's suppose a percent, 75% OK?)
If the number required is larger than the answer you worked out (because you've only got 75% product from a particular process and you need to work out the amount of reactant, for example) then you multiply it by 100/75
But if the number is smaller than what you worked out (for example, because the process is 75% efficient), then multiply it by 75/100!
Sorry StringFever, could you (or someone else) explain that again?
I remember a VCAA paper that had 60% efficiency for some hydrogen cell. And, instead of multiplying by 0.6, you had to divide by 0.6. Why is this so?
It took me a while to get and I just wanna go over it again =\
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Oh, also fun fact of the day - did you know nuclear fission is endothermic in the sun between elements from hydrogen to iron :)
Why u say between those elements its endothermic, theyre the only elements the sun can consist of, nothing heavier exists within a sun.
False. In a dying star, lots of things can happen. (Stars are universal element factories, they convert hydrogen to helium to lithium and keep going until Iron, in their healthy lifespan. Just before they completely die, they spit out the heavier more exotic elements such as lead, uranium, etc, basically everything in the periodic table).
Thats weird I thought that it goes up to iron only when its dying and while its healthy it simply converted hydrogen to helium (I better go bak to the drawing board).
I thought once the sun got up to iron, the star was choked under the hihg weight of iron and then proceeded to die (but maybe that is the phase before becoming a red giant).
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Efficiency-style questions:
(Let's suppose a percent, 75% OK?)
If the number required is larger than the answer you worked out (because you've only got 75% product from a particular process and you need to work out the amount of reactant, for example) then you multiply it by 100/75
But if the number is smaller than what you worked out (for example, because the process is 75% efficient), then multiply it by 75/100!
Sorry StringFever, could you (or someone else) explain that again?
I remember a VCAA paper that had 60% efficiency for some hydrogen cell. And, instead of multiplying by 0.6, you had to divide by 0.6. Why is this so?
It took me a while to get and I just wanna go over it again =\
This is assuming that you had to find the hydrogen used in the cell, right?
Because if we think about it, the cell was 60% efficient right - therefore, only 60% of the hydrogen was used to produced energy.
For us, we've only got data about the energy produced from the cell, and that's 60% of the hydrogen used.
Since the actual amount of hydrogen is greater, we need to multiply by (100/60) which is the same as dividing by 0.6! :)
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
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yeah, that 100/60 got me confused initially. Cos i remember doing 60/100 in year 11, all the way through that year. then this year, we had to do it the other way round. so yeah.
is it ALWAYS 100/x, x being efficiency percentile?
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
I find the easiest way to do alkaline-based half-equations is to balance it as if it were in an acidic solution (so with H+ ions), and then after that, balance both sides with the same number of OH- ions. In doing so, the H+ and OH- will form water, and all you need to do is clean it up and you have your basic half-equation.
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
I find the easiest way to do alkaline-based half-equations is to balance it as if it were in an acidic solution (so with H+ ions), and then after that, balance both sides with the same number of OH- ions. In doing so, the H+ and OH- will form water, and all you need to do is clean it up and you have your basic half-equation.
This = the chemguide way :)
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
I find the easiest way to do alkaline-based half-equations is to balance it as if it were in an acidic solution (so with H+ ions), and then after that, balance both sides with the same number of OH- ions. In doing so, the H+ and OH- will form water, and all you need to do is clean it up and you have your basic half-equation.
can you give an example please?
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
Give me an example question and I'll do it for you! :)
I find the easiest way to do alkaline-based half-equations is to balance it as if it were in an acidic solution (so with H+ ions), and then after that, balance both sides with the same number of OH- ions. In doing so, the H+ and OH- will form water, and all you need to do is clean it up and you have your basic half-equation.
can you give an example please?
OK, let's take Zn to Zn(OH)2.
Step 1: Set up skeleton equation
Zn --> Zn(OH)2
Step 2: Balance like in acidic environment (with H+s and waters)
Zn + 2H2O --> Zn(OH)2
Zn + 2H2O --> Zn(OH)2 + 2H+ + 2e-
Step 3: Balance any H+ with an OH- (ON BOTH SIDES)
Zn + 2H2O + 2OH- --> Zn(OH)2 + 2H+ + 2e- +2OH-
Step 4: H+ and OH- form water
Zn + 2H2O + 2OH- --> Zn(OH)2 + 2H2O + 2e-
Step 5: Clean it up and voila
Zn + 2OH- --> Zn(OH)2 + 2e-
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
half reactions in alkaline conditions are harder to do
i recommend this
http://www.chemguide.co.uk/inorganic/redox/equations2.html
explains how to do it very well, with some good examples
the main point is that sometimes it is a little difficult to know whether to add OH- or H2O first, but if you do it as if it was under acidic conditions and then cancel out the hydrogen ions by adding OH- to each side, it works out
read some of their examples and you'll see what i mean
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thanks stringfever and homghomg1 ;)
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Hey u know for redox reactions how for acidic medium you add
then
, does it work the opposite way for alkaline medium? I've done a few examples adding
first and then
but is that how you're meant to do it?
half reactions in alkaline conditions are harder to do
i recommend this
http://www.chemguide.co.uk/inorganic/redox/equations2.html
explains how to do it very well, with some good examples
the main point is that sometimes it is a little difficult to know whether to add OH- or H2O first, but if you do it as if it was under acidic conditions and then cancel out the hydrogen ions by adding OH- to each side, it works out
read some of their examples and you'll see what i mean
Like my example above :)
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In an equilibrium reaction:
: (the crappy graph below shows the species at equilibrium)
A|___
B|___
C|___
|___:_________
t
At time t, if we add a little concentration of B, B spikes up but as it establishes equilibrium again, its concentration is higher than before you added it. A gradually goes up and establishes equilibrium. But what happens to C? In a trial exam, it shows that C spikes up as well (but not as much as B) and goes back to being the same concentration again. Is this right?
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That's odd, I would have thought that [C] would decrease since you have a net back reaction o.O
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Exactly. That's what I thought as well. This was a NEAP trial exam.
LOL learning from trial exams like this will screw me over =\
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I pretty sure [C] does not spike up, it just decrease right from when more B was added. hmmmm...
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wow...thats an excellent way of balancing alkaline solutions. never knew that. thnx .
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- An equation
does not imply that the concentration graphs will start with
NO! You must look at the equilibrium constant!
Okay, in relation to this^
If we have
, with
, how do you know which lines corresponds to which species?
I looked at the concentration of the three to determine it (which was the correct answer) but wasn't sure how to use the equi. constant.
Thanks
Edit: oops stuffed the LaTeX up for the equi constant =\
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Oops, maybe that was a bit misleading, usually they won't give you enough information to work it out from the equilibrium constant, so you have to try to use this:
"- In
, any changes driven by LCP will involve the graphs increasing/decreasing in ratio 1:2:1 for A:B:C
respectively. i.e. the number in front of the chemical will govern how much the graph of that chemical increases/decreases due to LCP."
Which basically means they have to DO something to the equilibrium so you can observe the change.
e.g. If they put in extra reactant A, then graph A will spike up but then graphs A and B will decrease, but B will decrease twice as much as A, so that's how you tell A and B apart. Also, C will increase and that's how you locate C
e.g. If they dilute the solution then all 3 will decrease, but then A and B will increase, with B increasing twice as much as A. C will decrease.
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Ah! Thank you /0. I understand now :)
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You know the electrochemical series?
Well if the equations happen in reverse, does that mean the electrovoltage becomes the opposite charge (i.e + to -)
Say for example if  = 2.87 V)
would
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Hmm I don't think that applies to the electrochemical series, only enthalpies etc.
As long as you have the difference in potentials
you can find out how much voltage is produced by a spontaneous reaction or how much voltage is required to drive a non-spontaneous reaction.
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Hmm I don't think that applies to the electrochemical series, only enthalpies etc.
As long as you have the difference in potentials
you can find out how much voltage is produced by a spontaneous reaction or how much voltage is required to drive a non-spontaneous reaction.
Thanks, ths electrocehmical stuff is soo hard, I much prefer LPG.