April 19, 2024, 04:54:22 AM
Forum Rules: Read This Before Posting


Topic: Reaction of cyclohexylmagnesium bromide and benzyl bromide  (Read 1158 times)

0 Members and 1 Guest are viewing this topic.

Offline mglbs

  • Regular Member
  • ***
  • Posts: 11
  • Mole Snacks: +0/-0
Reaction of cyclohexylmagnesium bromide and benzyl bromide
« on: February 19, 2021, 11:54:49 AM »
Can anyone help me with the following reaction?
I have no idea how to solve it.

Offline chenbeier

  • Sr. Member
  • *****
  • Posts: 1348
  • Mole Snacks: +102/-22
  • Gender: Male
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #1 on: February 19, 2021, 12:35:58 PM »
The magnesium likes  the bromine. So what will be left if magnesiumbromide is gone?

Offline mglbs

  • Regular Member
  • ***
  • Posts: 11
  • Mole Snacks: +0/-0
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #2 on: February 19, 2021, 12:41:22 PM »
The magnesium likes  the bromine. So what will be left if magnesiumbromide is gone?

Only cyclo hexane or?

Offline chenbeier

  • Sr. Member
  • *****
  • Posts: 1348
  • Mole Snacks: +102/-22
  • Gender: Male
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #3 on: February 19, 2021, 12:49:01 PM »
No, do you know the Wurtz reaction. Where did you left the benzyl group.

Offline mglbs

  • Regular Member
  • ***
  • Posts: 11
  • Mole Snacks: +0/-0
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #4 on: February 19, 2021, 12:59:43 PM »
No, do you know the Wurtz reaction. Where did you left the benzyl group.

I'm not sure. Is it (Cyclohexylmethyl)benzene?

Offline chenbeier

  • Sr. Member
  • *****
  • Posts: 1348
  • Mole Snacks: +102/-22
  • Gender: Male
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #5 on: February 19, 2021, 01:06:27 PM »
Correct or Benzyl-cyclohexane

Offline BjornS

  • Regular Member
  • ***
  • Posts: 9
  • Mole Snacks: +0/-0
Re: Reaction of cyclohexylmagnesium bromide and benzyl bromide
« Reply #6 on: February 20, 2021, 04:20:36 AM »
Are you familiar with the term "grignard reagent"? The molecule on the left side of the arrow is one (simplified with: RMgX (R=carbonchain, X=halogene)).

The Br molecule which is attached to toluene (simplified as RX) reacts as a leaving group when RMgX attacks it.

I think chenbeier made it all clear to you yesterday. But  maybe this makes it more clear.

Also a tip: If you get a question where bromocyclohexane reacts with Mg (as the reagent) it will also form the molecule on the left side of the arrow.

Sponsored Links