Got to love this. A comprehensive infographic detailing the smells of organic compounds.
Download
Sit back
and enjoy telling one of your non-chemistry studying friends that they smell of Octanoic acid
Thursday, October 2, 2014
Sunday, June 15, 2014
Electrode Potential Comedy
Electrode 1: Oh no! I think those electrons are coming my way.
Electrode 2: Are you sure?
Electrode 1: Yes, I'm positive!
Explanation (if you need one)
Which way do electrons flow in a cell?
Towards the positive electrode.
Friday, June 13, 2014
Slowly, Slowly, Catchee Monkey (or Rate Determining Step)
So, you have written your rate equation and the next question asks you to suggest a rate determining step.
The key phrase here is suggest, when ever you see this the examiner is telling you that there are lots of possible answers, you just have to come up with one of them. There is an implication in the word "suggest" that there is some educated guess work involved.
So what do you suggest?
Let's look at an example...
Here is an overall reaction
![](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_t-VPmq9hiP660nuzVu5Gd3wugvlizJMSem8U4ncoUW7wJ3GLmLHZfrhtI4MFNgrQaYqZQr55v8m2R-lIthJrKCRyiYkAA2tY3vTYZnwS935-DWJoDkI3_xWEUiJVJ9PA=s0-d)
Here is the rate equation
![](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_uSCejaXgnkGSCSqvYoSWyU_wS5SJnJXdo_z2xqxeQKO_UG7N532U0QXgcvzvufFiYXyRfmWvyxrxUJGoKIZnIhZwNyrff4yc4vvnqTDcP5cwk0pgL2n3NX3AW_Wg=s0-d)
Question - Suggest a rate determining step.
In this relatively simple example, the rate equation tells me that the OH- isn't involved in the slow step. It is only the (CH3)3CBr. The implication is that the OH- comes in to play in some unknown later fast step, I guess theoretically it could be involved in an earlier fast step but realistcally what can OH- do on its own in a first step?
So, all we know is that the rate determining step has (CH3)3CBr as a reactant and nothing else, giving us...
(CH3)3CBr -->
What about the products?
Well you would get away with "intermediates", i.e.
(CH3)3CBr --> intermediates
but in this question you can do better than that
because if all you have is one molecule of (CH3)3Br on its own it must fall apart and logically what must fall off is the Br-. As it is a product in the full equation. This gives us
(CH3)3CBr --> (CH3)3C+ and Br- as the slow (rate determining) step
and then theoretically
(CH3)3C+ and OH- --> (CH3)3COH as the the fast step.
Will that get you the marks in the exams? Yep
Is that what really happens? Doesn't matter
The key phrase here is suggest, when ever you see this the examiner is telling you that there are lots of possible answers, you just have to come up with one of them. There is an implication in the word "suggest" that there is some educated guess work involved.
So what do you suggest?
Let's look at an example...
Here is an overall reaction
Here is the rate equation
Question - Suggest a rate determining step.
In this relatively simple example, the rate equation tells me that the OH- isn't involved in the slow step. It is only the (CH3)3CBr. The implication is that the OH- comes in to play in some unknown later fast step, I guess theoretically it could be involved in an earlier fast step but realistcally what can OH- do on its own in a first step?
So, all we know is that the rate determining step has (CH3)3CBr as a reactant and nothing else, giving us...
(CH3)3CBr -->
What about the products?
Well you would get away with "intermediates", i.e.
(CH3)3CBr --> intermediates
but in this question you can do better than that
because if all you have is one molecule of (CH3)3Br on its own it must fall apart and logically what must fall off is the Br-. As it is a product in the full equation. This gives us
(CH3)3CBr --> (CH3)3C+ and Br- as the slow (rate determining) step
and then theoretically
(CH3)3C+ and OH- --> (CH3)3COH as the the fast step.
Will that get you the marks in the exams? Yep
Is that what really happens? Doesn't matter
Friday, June 6, 2014
Which way do you flow?
OK let's talk cells.
EMF to be specific. How do you know which way things are going to go?
It all comes down to EMF. The EMF, just to remind you, is that thing you work out where you draw the cell put in the the Eo values, go against one and with the other and eventually you get a voltage. Remember? If not, go revise.
EMF = positive --> electrons flow left to right --> right electrode is positive (because electrons flow towards the positive)
EMF = negative --> electrons flow right to left --> left electrode is positive (because electrons flow towards the positive)
Mine's a double
How do you know which values to double when doing Born-Haber Cycles?
Simple really.
In a compound like CaCl2, you always have to deal with 2 chlorines so any value which refers to chlorine will need to be doubled to make it refer to 2 chlorines.
In this case that will be the enthalpy of atomisation
1/2 Cl2 (g) --> Cl (g) needs to be doubled
and
enthalpy of electron affinity
Cl + e- --> Cl- needs to be doubled.
The possibility is in something like Na2O, now you are dealing with 2 sodiums so you would need to double the sodium values, i.e.
enthalpy of atomisation
Na (s) --> Na(g) needs to be doubled
and
enthalpy of ionisation (energy)
Na --> Na+ + e- needs to be doubled
It is worth being careful though as every now and again they pre-double some things for you in the table, so have a read and double only if it refers to one Na (or whatever) and you need it to be 2.
It's at time like this that I wish blogspot did superscript and subscript.
What colour is a giraffe's tongue and spit?
Blue?
Black?
Blue/Black?
So if in an exam question they ask what colour is Iodine Starch complex. Go Blue, black, blue/black. It's all the same to the average giraffe (or examiner)
Thursday, June 5, 2014
What colour is Chromium 3+?
Have you ever wondered what colour Chromium 3+ is?
If you haven't then fine, move on.
If not take a look at this
This is Chromium 3+
That look about right doesn't it.
Green.
The colour of the positive test for alcohols, orange to green
All nice and straight forward.
but look at this...
This is Chromium 3+
Confused.
Let me explain.
Chromium 3+ with only water ligands is in fact this violet colour seen above but if there are any other possible ligands present then it will turn green.
So, what about in the dichromate to chromium 3+ test for alcohols? In that case, there is the presence of Cl- or SO4 2- ions (from sulphuric acid or hydrochloric acid used to acidify the solution) which replace the water and make it look green.
So, what colour is chromium 3+? purple, if it is on its own, or green if some nice looking anions swing by.
If you haven't then fine, move on.
If not take a look at this
This is Chromium 3+
That look about right doesn't it.
Green.
The colour of the positive test for alcohols, orange to green
All nice and straight forward.
but look at this...
This is Chromium 3+
Confused.
Let me explain.
Chromium 3+ with only water ligands is in fact this violet colour seen above but if there are any other possible ligands present then it will turn green.
So, what about in the dichromate to chromium 3+ test for alcohols? In that case, there is the presence of Cl- or SO4 2- ions (from sulphuric acid or hydrochloric acid used to acidify the solution) which replace the water and make it look green.
So, what colour is chromium 3+? purple, if it is on its own, or green if some nice looking anions swing by.
Sunday, May 4, 2014
Cheshire, Felix, Garfield, Tom, Pilchard, Scratchy, Stimpy, Sylvester, Snowball
What do this bunch have in common?
Do they speed up reaction? Nope
Do they manage to not get used up in reactions? Probably not
Do they allow alternative pathways? Nope
Are they unchanged during a reaction? Nope
Do they change the position of an equilibirum? erm, well, no, probably not
because they are a "list-of-cats" and not "catalysts"
(Apologies, possibly worst intro ever, let's move on)
Catalysts (unlike lists of cats) are useful industrially for a number of reasons. New catalyst development is part of what is called green chemistry. Let's run through the uses of catalysts one by one...
Anybody not feeling sick having watched that whale explode a dozen times. Try this fact.
Beached whales tend to explode due to a build up of a combination of methane, hydrogen sulphide and ammonia. So it effectively smells of farts, stink bombs and urine.
No wonder the tango man runs.
Do they speed up reaction? Nope
Do they manage to not get used up in reactions? Probably not
Do they allow alternative pathways? Nope
Are they unchanged during a reaction? Nope
Do they change the position of an equilibirum? erm, well, no, probably not
because they are a "list-of-cats" and not "catalysts"
(Apologies, possibly worst intro ever, let's move on)
Catalysts (unlike lists of cats) are useful industrially for a number of reasons. New catalyst development is part of what is called green chemistry. Let's run through the uses of catalysts one by one...
- Allow usage of lower temperatures
- Allow usage of lower pressures
If somebody asked you the question - What does Airbus make? I am sure you would say the answer aeroplanes, but you would be wrong, Airbus make money, aeroplanes are merely the medium they use. So, for any manufacturing company, cost saving is important and by reducing the temperature and pressure required in their factories they lower energy costs.
Additionally, reducing energy usage reduces greenhouse emission in power plants (less energy = less CO2 made.
Finally, lowering pressure makes your factory safer to operate. You don't want to be around when a high pressure vessel (whale based or otherwise) explodes.
3. New production routes and products become possiblePut simply new catalysts = new chemicals and new ways of making chemicals. Why this is important will vary from scenario to scenario, it could be cheaper, it could involved less toxic reactants or by products, it could be a new chemical that is better at its intended job etc.
Anybody not feeling sick having watched that whale explode a dozen times. Try this fact.
Beached whales tend to explode due to a build up of a combination of methane, hydrogen sulphide and ammonia. So it effectively smells of farts, stink bombs and urine.
No wonder the tango man runs.
IT'S A BOMB!!!!!!
Ever wondered what exactly a bomb calorimeter is? Well, this is a bomb calorimeter.
It is basically a really, really, really well insulated container full of water that contains another container inside it that can burn any chemical to completion without losing any heat (well, very, very, very little heat).
Not impressed? Thought it would be a bit more James Bond? 'Fraid it is more Borne-Haber than Bourne Identity (Google it)
What is the point of it?
By using a Bomb Calorimeter, you can very accurately measure the enthalpy of combustion because no heat is lost to the environment, it is all used to raise the temperature of the water.
What do you need to know about it for CH1?
Very little, only that it is an improvement over using a polystyrene coffee cup and a plastic lid with a thermometer pushed through it
Hold on, just had a thought, if you used a bomb calorimeter to keep your coffee in, it would stay hot forever! Why hasn't somebody else thought of this? Infinity Coffee! It could be a big seller, you heard it here first.
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