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Topic: Question about intramolecular vs. solvent effect  (Read 3218 times)

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Offline afweaser

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Question about intramolecular vs. solvent effect
« on: November 08, 2008, 11:25:43 PM »
I have a question regarding the effect of solvent vs. intramolecular attack on a compound. For example, if you have a secondary carbocation and it is attached to a string of 2 carbons and at the end is a hydroxyl group, will the hydroxyl group attack the carbocation and form a ring structure, or will a water molecule from the aqueous acidic solvent attack the carbocation and the compound will end up with two hydroxyl groups? Thanks so much.

Offline nj_bartel

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Re: Question about intramolecular vs. solvent effect
« Reply #1 on: November 08, 2008, 11:47:36 PM »
A good general rule is that intramolecular forces take place faster than intermolecular forces, so the ring would probably be favored.

Offline afweaser

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Re: Question about intramolecular vs. solvent effect
« Reply #2 on: November 09, 2008, 09:18:11 AM »
Is that true even if the molecule is surrounded by lots of aqueous solvent?

Offline nj_bartel

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Re: Question about intramolecular vs. solvent effect
« Reply #3 on: November 09, 2008, 12:22:38 PM »
I just learned that as a general rule - I'm not sure what exceptions apply.

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