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Tagged with hydrogen-bond alcohols
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Water solubility comparison of stereoisomers of bicyclo [4.4.0] decane-3,4-diol
I think, (I) must be more soluble in water. It is due to trans configuration and thus, forming more effectively inter-molecular hydrogen bonds with water molecules.
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Why does energy need to be "compensated" in order for solvation to occur?
I am currently learning about the physical properties of alcohols.
I understand that the main intermolecular forces between alcohols and water are hydrogen bonds. When these two are mixed, the ...
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