Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: SheffieldWednesday4ever on September 15, 2009, 07:56:13 PM
-
Hei everyone,
I am new but I was wondering if anyone could help me with this problem
I need a way to separate a mixture of para-nitrophenol and naphthylene by exploiting their different solubilities.
Thanks
-
You have to show your attempts to receive help. This is a forum policy.
Check what ARE their solubilities in diffrent pHs and in different solvents.
-
Okay sorry. I've read the rules now.
Based on my question, it tries to get me to consider the functional groups of the two molecules. I understand that the P-nitrophenol is very acidic because the NO2 is a strong electron withdrawing group to make the Oxygen less negative. Therefore, the hydrogen wants to leave. So if I added say, an aqueous solution of Na-OH, the p-nitrophenol would be de-protonated and the phenol would be dissolved in the water.
But for the naphthylene, there seems to be many ether groups. So if I mix a solution of ether with a solution of Na-OH, would the two compounds be separated? Or is there a better/right way?
Thanks again