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Topic: Recovering by Dilution with Water  (Read 1516 times)

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Offline RedsAreRaw

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Recovering by Dilution with Water
« on: December 30, 2016, 04:04:26 PM »
Hello everyone,
     I am just starting to work through a Morrison and Boyd 3rd edition Organic Chemistry book and thought discussion forums to be a good place to discuss and ask questions as I progress. One question I came across is: Account for the fact that nearly every organic compound containing oxygen dissolves in cold concentrated sulfuric acid to yield a solution from which the compound can be recovered by dilution with water.

Is the reason for this because the more water you add the more HSO4- you are getting rid of? Then ending with your product and water?

Thanks

Offline AWK

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Re: Recovering by Dilution with Water
« Reply #1 on: December 30, 2016, 05:00:18 PM »
This probably concerns compound insoluble in water that are protonized by a concentrated sulfuric acid.
AWK

Offline RedsAreRaw

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Re: Recovering by Dilution with Water
« Reply #2 on: January 09, 2017, 10:47:16 AM »
Yeah that makes sense.

Thanks AWK for the quick reply!

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