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The melting point for lauric acid is about 45 degrees while it is 121 degrees for naphthol. So, in a mixture repeated cycles of slow warming and cooling should separate out lauric acid from naphthol. You can improve the efficiency by adding a dash of slightly acidic 70% isopropyl alcohol. This will deprotonate the lauric acid while maintaining the proton on naphthol during this process to enhance separation and purification of the two compounds. You could also flat-out distill the two products by maintaining the temperature of the solution at the boiling point of lauric acid to separate it from naphthol.

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13y ago
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13y ago

Benzophenone is soluble in cyclohexane, but a-naphthol is insoluble in cyclohexane. Therefore, you can dissolve the benzophenone in the cyclohexane, and then filter or decant for the a-naphthol.

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15y ago

You can add cyclohexane to the mixture. a-naphthol is insoluble in cyclohexane while lauric acid is soluble in cyclohexane.

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10y ago

Distillation, since the boiling pt of acetone is much higher.

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16y ago

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Q: How could you seperate benzophenone from a-naphthol?
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