January 07, 2025, 04:16:54 PM
Forum Rules: Read This Before Posting


Topic: Having difficulty with alkene addition reactions  (Read 1831 times)

0 Members and 1 Guest are viewing this topic.

Offline heycoa

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Having difficulty with alkene addition reactions
« on: July 16, 2013, 11:07:58 AM »
Here is the image:



I am trying to solve the reaction by mono substitution but I do not think that is correct.  Please *delete me*

Mod edit: Please use img tags like this: [img]http://image uri[/img] or upload images as attachments (click the "Additional Options..." tab below the edit field in the reply window) or use SMILES code - please do not link to external image hosting websites. For more information on formatting posts correctly, click here. Dan
« Last Edit: July 16, 2013, 12:20:16 PM by Dan »

Offline heycoa

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Re: Having difficulty with alkene addition reactions
« Reply #1 on: July 16, 2013, 11:22:51 AM »
I actually figured it out.  The double bond breaks down. 

Offline magician4

  • Chemist
  • Full Member
  • *
  • Posts: 567
  • Mole Snacks: +70/-11
Re: Having difficulty with alkene addition reactions
« Reply #2 on: July 16, 2013, 12:06:19 PM »
that's correct: HBr will add to the double bond (and hence the double bond will "break down")


but that's only half of the story, presumably: where will the proton go and why  (followed by bromide - addition to the resulting carbocation) ?  that's two different products resulting thereof,  either way!

 :rarrow: this bit seems to me to be the core of the problem given to you


 :rarrow: you're only halfway there, if that much


regards

Ingo
There is a theory which states that if ever anybody discovers exactly what the Universe is for and why it is here, it will instantly disappear and be replaced by something even more bizarre and inexplicable. There is another theory which states that this has already happened.
(Douglas Adams)

Sponsored Links