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Topic: Doubt about resonance - thiol oxidation  (Read 5763 times)

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Offline Sosi

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Doubt about resonance - thiol oxidation
« on: November 27, 2009, 09:47:26 AM »
Hi!

I have the reaction between a thiol (RS-H) and hydrogen peroxide (H2O2). I want to sketch this oxidation process:

RS-H + H2O2  :rarrow: RS-OH + H2O

I draw the whole reaction scheme, but since I dont know how to draw it digitally, ill just explain all the steps:

RS-H + HOOH :rarrow: RS- + OH+ + H+ + OH- :rarrow: RS-OH + H2O

Is this correct? Thanks a lot for all the help

Offline tmartin

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Re: Doubt about resonance - thiol oxidation
« Reply #1 on: November 27, 2009, 09:57:18 AM »
I don't believe that RS-H --> RS- H+ in solution without some added help.  Also I would avoid thinking of H2O2 going to OH+ and OH- spontaneously.  Although if you think about the reaction in terms of nucleophilic species and electrophilic species it may help get the ball rolling for the mechanism.

Offline Sosi

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Re: Doubt about resonance - thiol oxidation
« Reply #2 on: November 27, 2009, 10:12:15 AM »
I gave some more thought, and I believe the mechanism should go like this:

R-S-H + H2O2 :rarrow: R-S-O-H + H+ + OH-  (in this step, the electrons that bond sulfur to hydrogen will attack one of the oxigens of H2O2 (leaving a proton available to react), and the bond that links the two oxigens of the H2O2 will attack one of its oxigens, producing hydrogen peroxide. This will then lead to:


R-S-O-H + H+ + OH- :rarrow: R - S - OH + H2O (in this step, the extra electrons in the hydroxyde group will attack the free proton).



Are my thoughts correct?
Thanks

Offline tmartin

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Re: Doubt about resonance - thiol oxidation
« Reply #3 on: November 27, 2009, 10:22:34 AM »
This time you are closer,  you have the correct nucleophile and electrophile.  Remember that sulfur (like oxygen) has lone pairs of electrons.  Those electrons can push into the O-O bond to break it and form the S-O bond.  This would leave a positive charge on sulfur and a negative charge on the displaced oxygen.

Offline Sosi

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Re: Doubt about resonance - thiol oxidation
« Reply #4 on: November 27, 2009, 10:25:19 AM »
This time you are closer,  you have the correct nucleophile and electrophile.  Remember that sulfur (like oxygen) has lone pairs of electrons.  Those electrons can push into the O-O bond to break it and form the S-O bond.  This would leave a positive charge on sulfur and a negative charge on the displaced oxygen.

I see! Thanks so much!

By the way, how did you write that reaction scheme? I was trying to use chemdraw, but I can't seem to find how to put the unbonded valence electrons in the atoms.
Thanks

Offline tmartin

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Re: Doubt about resonance - thiol oxidation
« Reply #5 on: November 27, 2009, 10:30:19 AM »
No problem.  When you're looking at the toolbar, it is the same button that allows for charges to be placed, "Chemical Symbols Tool".  It may be that I just used the notation for a carbene, but the two little dots seem to serve the same purpose regardless. 

Offline Sosi

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Re: Doubt about resonance - thiol oxidation
« Reply #6 on: November 27, 2009, 10:32:52 AM »
Yep!

I got it now!  ;) I had organic chemistry too long ago and couldn't remember this kind of stuff anymore lol. Thanks once again

Offline orgopete

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Re: Doubt about resonance - thiol oxidation
« Reply #7 on: November 28, 2009, 01:46:16 AM »
I believe RSOH products are unstable and give RSSR + H2O as the products, but that wasn't your question.
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Offline Sosi

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Re: Doubt about resonance - thiol oxidation
« Reply #8 on: November 28, 2009, 06:23:36 AM »
I believe RSOH products are unstable and give RSSR + H2O as the products, but that wasn't your question.

Yes, this is one of those cases. After this oxidation it will lead to the formation of a dissulfide bond OR to the overoxidation (it forms RSO2H).
:D

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