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Topic: Help understanding why I'm gettnig these Sn2 exercises wrong?  (Read 1348 times)

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Offline frankenstein18

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Help understanding why I'm gettnig these Sn2 exercises wrong?
« on: November 15, 2015, 12:28:07 AM »
I'm studying Sn2 reactions and I know that Iodine is a weaker base and therefore a better leaving group than Br

In an exercise in my book (essential organic chem 3rd edition by paula yurkanis bruice) it asks to see which is more reactive between 1-bromo-2 phenylethane and 1-iodo-2 phenylethane

1-bromo-2 phenylethane and 1-iodo-2 phenylethane look pretty much the same except that one has Br and the other has Iodine

I thought it was 1-iodo-2 phenylethane because it has a better leaving group but the back of the book says its 1-bromo-2 phenylethane

Does the book have an error or am I just not understanding?

Offline orgopete

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Re: Help understanding why I'm gettnig these Sn2 exercises wrong?
« Reply #1 on: November 15, 2015, 09:48:47 AM »
This looks like an error.
Author of a multi-tiered example based workbook for learning organic chemistry mechanisms.

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