Organic Question (TopScore)

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Darknight260

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[answer: E]

Ok, so I know that the carbocation could go under rearrangement in the Markovnikov addition, but why on earth would go from a secondary carbocation to a primary??? Was this question just simply asking for all of the "possible" products? Because to my understanding the amount of product C produced would be negligible to none, right?
 
This reaction is under kinetic/thermo control. Although they didn't specify the temperature, at higher temperatures, the more stable product dominates (choice C) because the di-substituted alkene has more hyper-conjugation.
 
Ahhh okay, I was completely overlooking the fact that the carbocation was resonance stabilized (dur!). But I did not know about that thermodynamic control. Thanks for clearing that up!
 
Try to remember that Butadiene goes into allylic resonance.

C=C--C=C is the structure. The hydrogen will add to the least substituted as you predicted in order to avoid a primary carbo-cation.

[ H-C--C(+)--C=C] Is the form you predicted!

BUT... It has a resonance form. [H-C--C=C--C(+)]
 
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