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Reverse-phase chromatography

Basic questions from students; resources for projects and reports.

4 posts Page 1 of 1
First of all hello everyone

I was very surprised to find out there is actually a chromatography forum, so this is great news.
My question is, in Reverse Phase Chromatography for a mixture of benzene and para-xylene which peak is the first? It is the most polar that comes out first of course but I can't exactly find out which of those 2 it is. The dipole moment for both of them is zero.

thanks in advance

Instead of the words "polar" and "non-polar", use the approximate equivalents "hydrophilic" and "hydrophobic" (since those have Greek roots).

In reversed-phase, hydrophilic (polar) molecules elute early and hydrophobic (non-polar) molecules elute later.

Comparing your molecules, would the addition of two methyl groups to benzene make the molecule more hydrophobic or more hydrophilic?
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374

Since I posted this I did some research
Turns out p-xylene is the most hydrophobic of the two
The solvent is MeOH/water 65/35 so I guess the benzene would be the fastest while the xylene would be slower in order to avoid the water...hmm

Very good!! :D
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
4 posts Page 1 of 1

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