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Ch. 12 - Alcohols, Ethers, Epoxides and ThiolsWorksheetSee all chapters
All Chapters
Ch. 1 - A Review of General Chemistry
Ch. 2 - Molecular Representations
Ch. 3 - Acids and Bases
Ch. 4 - Alkanes and Cycloalkanes
Ch. 5 - Chirality
Ch. 6 - Thermodynamics and Kinetics
Ch. 7 - Substitution Reactions
Ch. 8 - Elimination Reactions
Ch. 9 - Alkenes and Alkynes
Ch. 10 - Addition Reactions
Ch. 11 - Radical Reactions
Ch. 12 - Alcohols, Ethers, Epoxides and Thiols
Ch. 13 - Alcohols and Carbonyl Compounds
Ch. 14 - Synthetic Techniques
Ch. 15 - Analytical Techniques: IR, NMR, Mass Spect
Ch. 16 - Conjugated Systems
Ch. 17 - Aromaticity
Ch. 18 - Reactions of Aromatics: EAS and Beyond
Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition
Ch. 20 - Carboxylic Acid Derivatives: NAS
Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon
Ch. 22 - Condensation Chemistry
Ch. 23 - Amines
Ch. 24 - Carbohydrates
Ch. 25 - Phenols
Ch. 26 - Amino Acids, Peptides, and Proteins
Ch. 26 - Transition Metals
Alcohol Nomenclature
Naming Ethers
Naming Epoxides
Naming Thiols
Alcohol Synthesis
Leaving Group Conversions - Using HX
Leaving Group Conversions - SOCl2 and PBr3
Leaving Group Conversions - Sulfonyl Chlorides
Leaving Group Conversions Summary
Williamson Ether Synthesis
Making Ethers - Alkoxymercuration
Making Ethers - Alcohol Condensation
Making Ethers - Acid-Catalyzed Alkoxylation
Making Ethers - Cumulative Practice
Ether Cleavage
Alcohol Protecting Groups
t-Butyl Ether Protecting Groups
Silyl Ether Protecting Groups
Sharpless Epoxidation
Thiol Reactions
Sulfide Oxidation
Additional Guides
Hydroxyl Group

Same reagents as oxymercuration, except with alcohol as the nucleophile instead of water.

Concept #1: The Mechanism of Alkoxymercuation. 


Another way that we can synthesize Ether is through a reaction called alkoxymercuration and you might immediately notice that the sounds a lot like another reaction that you're supposed to know by now and that's oxymercuration so it turns out this is going to be the same exact mechanism as oxymercuration or Oxymerc except that in the top reagent in the oxymercuration step we're going to use alcohol as our nucleophile instead of water, OK? So what you can see is that the biggest difference here is this right here, I have alcohol in place of the water and that's going to make an ether instead of alcohol, OK? So let me just walk you guys through this mechanism really quick, so remember that we get is HG-OAC-OAC......Opps it came out weird OAC and in the first step what we do is the double bond attacks the mercury kicks out one of the OACs and the Mercury attacks back so what we wind up making is a bridge, an Ion bridge so what that's going to look like is like this where now I have a dotted partial bond to HG it's only attached to 1 OAC now, dotted partial and a positive chart, OK? And there should be actually a dotted partial bond here too and a positive charge, OK? So now we've got our intermediate, notice that we can't get any shifts because there's no carbocation and now this is the part that typically water would come in and attack which side do you remember? In this case I have a Markovnikov site here and I have an anti-Markovnikov site there which one would it attack? Markovnikov because that's going to be the one with the most positive character but instead of water what's actually going to attack is in this case ethanol, OK? So my water attacks......I'm sorry my ethanol attacks kicks out the HG And what I wind up getting is something looks like this and I'm going to try to fit in here where now let's say that the alcohol attacked from the bottom then I would draw that the HG the mercury attacks from top or not attacks but is now placed in the top, OK? Cool? Awesome stuff the end of the Oxymerc step, OK? In this case alkoxymerc because I used ethanol, OK? Then remember that we have a reduction step, the reduction step is just NaBH4 and OH negative and you don't need to know the mechanism for this so I'm just going to say don't need to know mechanism, OK? But what we do need to know that happens is that well number there is a positive charge in that O actually, OK? And what's going to happen is that I'm going to wind up reducing the mercury just to an H so this is going to become H, OK? And I'm going to wind up deprotonating my oxygen so now look what that turns into, it turns into ether, OK? Because now what I have is RoR, it's a weird looking ether but it is an ether so I get an ether as my product and that's it's the same as OxyMerc except that you have to just now you have to be aware every time you see an Oxymerc make sure that you look to see whether it's water or alcohol that's attacking because that will make a world of difference in terms of what your product looks like, alright? So I hope that made sense same as I did before we're just using alcohol instead, alright? So let's go ahead and move on.