Oxymercuration-Demercuration, also referred to as oxymercuration-reduction is slightly more confusing than that average alkene reaction. I think it's a combination of the extra steps, involvement of mercury, and the mysterious reduction by sodium borohydride. But don't let this confuse you.
The video below takes you through the entire reaction mechanism with step by step explanations of every moving arrow, regioselectivity, and reason for lack of carbocation rearrangement.
Watch this video on YouTube or read the transcript (coming soon)
Watch the previous Video: Ring Expansion via Methyl and Hydride Shift
Watch Next video: Alkoxymercuration-demercuration
Return to: Alkene Reaction Mechanism home page;
A says
What is the mechanism for Demercuration? I mean how Hg(OAC) gets replaced by hydrogen.
won says
will this be anti addition?
Karla says
These videos are very helpful! It would be helpful if you showed which steps are reversible vs. non reversible.
Hritik says
Nice explanation but shouldn’t H2O attack the carbon with more partial positive charge (better electropile/electron deficient region) i.e. 1 degree terminal C ?
a-a-ron says
why wouldn’t the h2o form a bond with the mercury instead of attacking a carbon that’s only partially positive? hg has a positive charge so to me it makes more sense that the h2o would attack the hg than the carbon.
Amira says
You helped me get an A in orgo 1 first time taking it! I think I watched every single one of your videos, thank you so much Leah!
Valeria says
The reaction is always a “Syn-Addition”?
Julie says
At the end of step 2 do you still have acetic acid as a product? Or is that somehow used up during the reduction mechanism?
Leah4sci says
Acetate/acedic acid is a side product
nick says
how can mercury have a pair of electrons? i thought its electron configuration was [xe]4f14 5d10 6s2
Leah4sci says
This is a tricky concept Nick and I think the reason most professors skip it. Don’t forget that d-shell electrons are high in energy and may be called upon to react at any point in the mechanism.
latha says
How can one compound be attached to two carbon atoms at same time ? Here HgOAc is attached to both primary and secondary?
Leah4sci says
One bond is not dependent on the second. Hg has the ability to form multiple bonds
latha says
Oh k thank you….. I love the way u teach
Leah4sci says
Thank you Latha
Jess says
THANK YOU! I am in OChem 1 and have been struggling through the alkene reactions. You explain this so simply and give fantastic explanations for WHY the intermediates like HgOAc form the two bonds in the molecule. Thank you again!!
Leah4sci says
Thanks Jess
dsrlington says
I cant play the video kindly send m link to the video
Leah4sci says
This is a YouTube video, if it doesn’t work for you check your browser settings or try another browser
david says
You are my new favorite teacher! videos are clear and informative.
Leah4sci says
Thank you David. Are you in Orgo 1 or Orgo 2?