00:01
So we are analyzing the allusion order of nine different compounds.
00:06
I've written them here.
00:07
And i've written them in 8 through i order so that it can be a little bit easier for us to reference them as we're analyzing them.
00:13
Right.
00:13
So the illusion process is about extracting material from another by cleaning or rinsing or washing a solvent.
00:22
So the ion exchange resins are removed to capture the ions.
00:28
Now we have these nine different compounds and we generally want to find the normal phase liquid chromatography.
00:47
So i'll just put normal phase lc and then we need to find the reverse phase liquid chromatography.
01:10
So first before we get to that, let's list these in terms of the order of illusion.
01:15
Well, not order evolution necessarily, but in terms of their polarity.
01:20
So the order of illusion is actually, so i'll say the order of illusion.
01:32
So that will be alcohol, alcohol halides.
01:52
And this is in terms of formation, you know, the illusion order.
01:58
That's going to be, it's alcohol highlights, then saturated hydrocarbons, and then unsaturated, hydrocarbons and then esters and ketones, amines, then alcohols, then phenols, and then acids.
02:50
So in that order, let's go ahead and figure out the polarity of each of these.
02:56
Well, let's list the polarities of each of these.
03:00
So first of all, butidine is non -polar.
03:09
Nhexane is non -polar.
03:14
Chloriform is moderately polar.
03:20
Toluline is non -polar.
03:32
Diatherether is moderately polar.
03:40
Sucinic acid is highly polar.
03:47
It's an acid.
03:50
Pentanol is moderately polar.
03:55
It's an alcohol.
03:59
And isoamyl acetate is moderately polar.
04:06
It's a base...