Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: mazing on January 19, 2019, 03:17:40 PM
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If i have a set of different polar organic compounds and different polar (protic and aprotic) solvents, how can i determine which compound will be the most soluble in each of the solvents? This without using any sort of tools such as a solubility predictor. What difference between the compounds should I note to determine the relative solubility of each?
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Do you have any ideas? I think hydrogen bonding ability, dipolmoment and large lipophilic parts in the molecule are important. Can you maybe post the structures here?
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Also, remember that sometimes things are truly miscible, not just soluble.