In this video, we're going to talk about an extremely important way to get rid of carboxylic
acids and that's called decarboxylation.
Decarboxylation is going to be a very important reaction for the rest of Orgo.
It's really important that you understand how to do it now.
The way that it works is that a beta-carbonyl carboxylic acid can decarboxylate in the presence
of heat.
What this does is it produces CO2 gas as a byproduct.
It evolves out of the material.
Now what a beta-carbonyl carboxylic acid is, it’s just that you have some kind of carbonyl
beta to your carboxylic acid.
When you heat that up, what’s going to wind up happening is that you literally cleave
the entire carboxylic acid off and it becomes CO2 gas, leaving only the carbonyl portion
behind.
Obviously we need to get to the mechanism for this because it doesn't really make sense
just drawn like that.
Let’s do the mechanism.
For this mechanism, it’s going to make a lot more sense if you do one thing, if you
rotate the bonds.
We’re going to rotate this bond up when I draw it because it’s going to make a lot
more sense with the mechanism.
I’m actually going to draw my OH facing like this and my carbonyl down.
But this is still the same exact molecule.
I just rotated it, and you should too.
When I draw this mechanism, it’s actually a series of four arrows and there's right
place to start, or no right place to end.
It’s all concerted.
But I like to start from the oxygen grabbing the H because that’s kind of an easy place
to remember for me.
I would start with the O grabbing this H. It’s going to start off like that.
If I make a bond, I have to break a bond because H can’t have two.
This single bond is going to give its electrons and become a pi bond between that carbon and
that O.
Now, that carbon has four bonds.
Instead of breaking the bonds to the carbonyl though, I’m actually just going to break
the single bond to the carbon completely.
Notice what this is going to do is it’s going to release my C with two O’s on it
because now there's no single bond connecting it to the alkyl group.
Finally, once I make that bond, I have to break this bond.
There you go.
Those are the four arrows.
What we wind up getting, this is a heat-mediated reaction.
I wind up getting something that looks like this.
R with an OH with a double bond, and I’m going to get CO2.
Now it makes sense why I get the CO2 gas.
It should even make sense why the carboxylic acid is gone.
What might be a little confusing for you is that I told you that you’d get a carbonyl
from this, and right now I have an alcohol.
That doesn't seem to make sense.
This is something that we're going to talk about a lot more, if you haven't talked about
it yet.
But there's something special about vinyl alcohols.
Does anyone remember?
What’s special about vinyl alcohol?
They undergo this completely separate special process called tautomerization.
If you want more information on tautomerization, I have an entire video for that.
There's an entire section of your textbook dedicated to tautomerization and enol chemistry.
This is called an enol.
Enol or enolate chemistry is a huge deal.
You’re going to get there if you haven’t yet.
But the whole point being that when you tautomerize, what you do is you switch the locations of
double bond and a hydrogen.
What this actually comes after tautomerization is this.
This is the keto form.
You wind up getting the ketone.
Just take my word for it that it tautomerizes and then you’re fine.
Awesome.
What I want you guys to do is for the next example, go ahead and predict what the product
would look like.
I know it’s a big complicated molecule.
Predict it and then I’ll explain what's going on.