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Topic: Are both of this mechanism possible?  (Read 2522 times)

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Offline snoopy396

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Are both of this mechanism possible?
« on: July 23, 2015, 02:49:28 AM »
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Offline Dan

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Re: Are both of this mechanism possible?
« Reply #1 on: July 23, 2015, 04:13:27 AM »
What is generally faster, an intermolecular reaction or an intramolecular reaction?
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Offline snoopy396

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Re: Are both of this mechanism possible?
« Reply #2 on: July 23, 2015, 01:37:53 PM »
I understand intramolecular rxns are generally faster I would like some feed back if both mechanisms are possible and yield the same product thank you

Offline kriggy

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Re: Are both of this mechanism possible?
« Reply #3 on: July 23, 2015, 05:00:16 PM »
If intramolecular reactions are faster, do you think the di-bromo compound will be formed before the intermolecular atack occurs?

Offline orgopete

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Re: Are both of this mechanism possible?
« Reply #4 on: July 23, 2015, 05:05:06 PM »
I understand intramolecular rxns are generally faster I would like some feed back if both mechanisms are possible and yield the same product thank you


Possible? Sure, but...


An element in understanding chemistry are collisions. When the kinetics of SN2 reactions are determined, concentration is a major factor. Doubling the concentrations doubles the rate. If one is comparing intra v intermolecular reactions, the proximity of an intramolecular interaction will be inherently greater. Certainly unproductive orientations may enable an intermolecular reaction to compete. However, when two mechanisms can lead to the same product, especially with very similar mechanisms, it would be very difficult to determine or exclude one or the other completely. If the choice were anion v cationic or ionic v radical, this would be easier to determine.
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Offline TheMantis

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Re: Are both of this mechanism possible?
« Reply #5 on: September 14, 2015, 01:12:17 AM »
I see a problem with mechanism 1.  Review your chapters on alkyl halides and elimination recations and tell yourself why it wouldn't work.

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