Practice: Predict the product of the following reaciton.
|Ch. 1 - A Review of General Chemistry||4hrs & 47mins||0% complete||WorksheetStart|
|Ch. 2 - Molecular Representations||1hr & 12mins||0% complete||WorksheetStart|
|Ch. 3 - Acids and Bases||2hrs & 45mins||0% complete||WorksheetStart|
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|Ch. 9 - Alkenes and Alkynes||2hrs & 10mins||0% complete||WorksheetStart|
|Ch. 10 - Addition Reactions||3hrs & 33mins||0% complete||WorksheetStart|
|Ch. 11 - Radical Reactions||1hr & 57mins||0% complete||WorksheetStart|
|Ch. 12 - Alcohols, Ethers, Epoxides and Thiols||2hrs & 34mins||0% complete||WorksheetStart|
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|Ch. 18 - Reactions of Aromatics: EAS and Beyond||4hrs & 31mins||0% complete||WorksheetStart|
|Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition||4hrs & 54mins||0% complete||WorksheetStart|
|Ch. 20 - Carboxylic Acid Derivatives: NAS||2hrs & 3mins||0% complete||WorksheetStart|
|Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon||1hr & 59mins||0% complete||WorksheetStart|
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|Addition Reaction||7 mins||0 completed|
|Markovnikov||5 mins||0 completed|
|Hydrohalogenation||7 mins||0 completed|
|Acid-Catalyzed Hydration||17 mins||0 completed|
|Oxymercuration||20 mins||0 completed|
|Hydroboration||27 mins||0 completed|
|Hydrogenation||7 mins||0 completed|
|Halogenation||6 mins||0 completed|
|Halohydrin||17 mins||0 completed|
|Carbene||13 mins||0 completed|
|Epoxidation||8 mins||0 completed|
|Epoxide Reactions||9 mins||0 completed|
|Dihydroxylation||9 mins||0 completed|
|Ozonolysis||7 mins||0 completed|
|Ozonolysis Full Mechanism||25 mins||0 completed|
|Oxidative Cleavage||8 mins||0 completed|
|Alkyne Oxidative Cleavage||6 mins||0 completed|
|Alkyne Hydrohalogenation||3 mins||0 completed|
|Alkyne Halogenation||2 mins||0 completed|
|Alkyne Hydration||6 mins||0 completed|
|Alkyne Hydroboration||3 mins||0 completed|
|Thermodynamics of Addition-Elimination Equilibria|
|Stereospecificity vs. Stereoselectivity|
|Oxymercuration-Reduction Full Mechanism|
|Hydroboration-Oxidation Full Mechanism|
|Simmons-Smith Addition Mechanism|
|Anti Vicinal Dihydroxylation|
|LiBr and Acetic Acid for Anti Vinyl Dihaldes|
|Addition Reagent Facts|
|Predicting Stereoisomers of Addition Reactions|
|Addition to Concave vs. Convex Rings|
This is an indentical mechanism to halogention, except with water as the nucleophile in the second step. Why would water prefer to react as a nucleophile over a halogen anion? Let’s find out.
Concept #1: General properties of halohydrin formation.
Now I'm going to talk about a reaction that's so similar to halogenation that a lot of people get it confused with halogenation. It's just a little bit different because, in this case, we're going to be adding a halogen in the presence of water to a double bond. And this reaction is going to be called a halohydrin formation. So let's go ahead and get started.
Basically, the general reaction is that I still have my double bond. I still have my diatomic halogen. The only difference is that I'm running this reaction in the presence of water instead of an inert solvent. I actually have water present. What that means is that the water is going to wind up interacting and my end product is going to give me an alcohol on one side and a halogen on the other. This molecule right here is called, as a functional group, it's called a halohydrin.
So let's go ahead and talk about the actual mechanism. The intermediate is once again going to be a bridged ion, just like before. The stereochemistry is going to be anti just like before because anytime you're opening up a three-membered ring, you're going to wind up getting anti products. And my product is going to be a halohydrin.
Are there going to be rearrangements? Nope. No rearrangements because there's no carbonyl, whoa, I said that completely wrong – no carbocation. And then finally, this actually will have Markovnikov regiochemistry because I am adding two different things. So now I do have to be aware of which one goes on the Markovnikov side and which one goes on the anti-Markovnikov side. But overall, we would say this is a Markovnikov reaction because it's driven by the stability of the intermediate.
Concept #2: A worked-example of the halohydrin mechanism.
So let's just go ahead and get started. The reaction is really straight forward. What I've got here is I've got the same situation where I've got a double bond and I've got a diatomic halogen and I've also got water, let's just say. I've also got water.
Which of these is going to react with my double bond? Well, water by itself doesn't really do anything to double bonds. Now if I had water and acid, that would be different, but this is just water by itself, so we can't really react water and a double bond. But we know that we can react a diatomic halogen. So I'm going to draw my three arrows once again, where the X is making a bridge to the double bond and it's also kicking out one of the X's as a leaving group. What this is going to give me is a bridged ion called a halonium ion, once again.
And now I just have to figure out what's the nucleophile that's going to do the back side attack or the nucleophilic attack of this ring. Basically, I've got two nucleophiles. I've got X-, just like before when we were talking about halogenation. We've got the X- just like before. Nothing has changed. But now what I also have is I've got some water lying around.
Now of these two different species, which of them do you think is going to be the stronger nucleophile? The X- or the water? What do you guys think? I've actually asked you guys a question like this before for another mechanism. The answer is that the X- is going to be much stronger. In fact, X- is one of the best nucleophiles around. Water is kind of like, eh because X- has a negative charge, water is neutral, so we would expect X- to be a lot stronger.
So why wouldn't I just get the X- attacking and get a halogenation reaction like before? Well, the answer is that I will. Some of that actually will happen. Some of the X- will attack and I will get halogenation. But, that's not going to be what happens the majority of the time. The majority of the time, this bridged ion is so unstable that it's going to react with the first nucleophile that it encounters, even if it's not the strongest.
And what if I have, once again, how about if I have a billion times more of the water than I have of the X-?So what if there's waters everywhere and there's only a few X-'s. What's going to wind up happening? Well, what's going to wind up happening is that even though the X- is stronger, the water is just going to have an advantage because there's a lot more of it around because when I planned out my reaction I used a little bit of diatomic halogen and I put a lot of water in there.
So what that means is that in this second step, even though the X- is more stable – is more nucleophilic, my water is going to wind up attacking the most substituted side. Does that make sense? Because there's just a whole lot more of it around.
Now for this water, is it going to attack the more substituted or the less substituted? It's still going to attack the more substituted side because that's the one with the most positive character and remember the water has the electrons on it. So I go ahead and I make that bond, I break that bond. And what that's going to give me is a major product that is a halohydrin. So if my water adds to the front then that means that my X is going to add to the back. That means that if my water was in the front, then my methyl group would also be towards the back.
Now is this my final product? No. I still have one more step, unfortunately, because I added water, so I need to deprotonate. I need to get rid of that H. What can I use to get rid of one of those H's? I could use the X-. So I'm going to use the X- in this last step to pull off an H and give the electrons to the O. So now what I'm going to get is a product that looks like this, a Markovnikov alcohol and an anti-Markovnikov halogen that's anti.
Do you have chiral centers here? Yup, so we have to draw both enantiomers. The other enantiomer would be the water attacked from the bottom, the methyl is now at the top and that means that my X is now at the top. And these would be a racemic mixture because I really have no clue which side it came from.
Does that make sense, guys? So I hope that you guys are able to see the similarities between halogenation and the halohydrin formation. The only difference is that I've got a lot of water around, so in that second nucleophilic attack, water is going to do the attack instead of the X-.
So let me know if you have any questions on that, but if not, let's go ahead and move on.
1. Electrophilic Addition
2. Nucleophilic Substitution (SN2) and Deprotonation
Practice: Predict the product of the following reaciton.
Practice: Predict the products of the following reaction.
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