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Would you expect the free base form of propane based alkaloids (atropine, cocaine, scopolamine) to be highly water soluble? Explain. What about their salt forms?

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As it can be observed from the structures, all 3 have similar structure: atropine, cocaine and scopolamine. Scopolamine is different from atropine just because epoxide group and stereochemistry on benzyl C atom while cocaine has a bit different structure but still very similar. Anyways, in order to determine if they are very soluble in water or not, it’s important which functional groups they have....

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