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Relative Stability of Amides Esters Anhydrides and Acyl Chlorides

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Relative Stability of Amides Esters Anhydrides and Acyl Chlorides

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I want to make a quick correction to the last video
where we introduced the carboxylic acid videos, and
then we can actually compare them in terms of their
relative stability.
And that one mistake I did is when I named the ester, all I
did is I named the main carbon backbone.
I didn't actually tell you how many carbons you have attached
to the oxygen over here.
Acetate really just refers to this part over here, knowing
that it is bonded to-- or maybe I should say it refers
to this part over here.
But you also have to specify how many carbons
you have over here.
So this molecule that we drew over here is
actually methyl acetate.
Or if you want it's systematic name, it's methyl ethanoate.
And this is where we get the methyl from.
It is methyl ethanoate.
Now, with that out of the way, let's actually compared these
carboxylic acid derivatives, and I'll compare the
derivatives of acetic acid.
So the first one we saw was the amide acetamide.
Acetamide looks just like this.
This is acetamide.
Then the next one we looked at was the ether.
And that's the one I just pointed out the mistake on.
So this was ethyl acetate.
You have CH3 right here.
This is methyl acetate.
This is where the methyl part comes from.
So this is methyl acetate.
And then we will compare that to the anhydride version.
So this is acetic anhydride.
Let me do this in a new color.
Acetic anhydride looks like this.
And finally, we had the acetyl chloride.
Acetyl chloride looked just like this.
And, of course, these are all derivatives of acetic acid,
which we drew at the top of the last video, which is right
over there.
Now, let's think about which of these may or may not be
more stable.
And to think about it, we're going to think about any
resonance structures that these molecules might have. So
if we first focus on acetamide, we know that
nitrogen forms three bonds and then has two extra electrons
that form another lone pair.
And it's actually electron rich, because it's a good bit
more electronegative than the hydrogens here and actually
reasonably more electronegative then the
carbon it's attached to.
So you could imagine a situation where a nitrogen
could donate an electron to this carbon right over here,
and then that carbon can let go of one of the electrons in
a double bond with the oxygen.
And so it could go back to the oxygen and you would have a
resonance structure that would look like this.
Let me actually use the same colors.
This oxygen just gained an electron up there.
And, actually, let me draw the electron.
Well, actually, I'll just put the negative charge due to
that electron.
And then we had this bond right
over here to the nitrogen.
But the nitrogen just a gave an electron to this carbon
right here, the carbonyl, or what was the carbonyl carbon,
and so now we have a double bond over here.
And the nitrogen just to gave an electron, so it now has a
positive charge.
But this is a resonance structure of acetamide, so
pretty stable.
So this is maybe I should even say quite stable.
Now, let's think about an ether here, and we could
probably do something fairly similar.
So if we think about this ether here, oxygen has two
extra lone pairs.
It is more electronegative than the things that it is
bonded to, so it could do a very similar thing to what
this nitrogen did.
It could give an electron to this carbon right over here,
and then that carbon can give back an electron to the
carbonyl oxygen, to that oxygen over there.
And so it's resonance structure
would look like this.
It would have a resonance structure, so it's almost the
exact same thing is as what we saw with the amide.
So it would have a resonance structure.
This oxygen just gained an electron.
Now it will have a negative charge.
This bond to the oxygen is still there, but this oxygen
just gave another electron, formed another bond with what
was the carbonyl carbon.
It actually forms a new carbonyl group, if you want to
view it that way, and so it will look like this.
And this oxygen gave away an electron so now it has a
positive charge.
So this seems like a pretty good resonance structure.
So the question is which of these two are
going to be more stable?
And the answer there really just comes out of
the Periodic Table.
If you look at nitrogen and oxygen, they're right there.
They're both near the top right.
They're both pretty electronegative, but oxygen is
more electronegative.
It is to the right of nitrogen.
So because oxygen is more electronegative, remember,
electronegativity is just the tendency to hog electrons.
How much do you like to hog electrons?
Oxygen likes to hog electrons more than nitrogen likes to
hog electrons.
So it would be less likely, marginally less likely, to
give away an electron than nitrogen would be, so this
resonance structure is a little bit less likely, or
when you think of it probabilistically, it's going
to happen a little bit less frequently than
this resonance structure.
So this one right here, this is going to stabilize it less.
So this is going to be a little bit less
stable then the amide.
So if we called this quite stable, I'll just say this is
just stable over here.
Now let's think about what's going to
happen with the anhydride.
The anhydride, once again, we have an oxygen right here.
It's got its spare electrons.
It's more electronegative than the things
that it's bonded to.
So it seems like you could do something very similar to what
we saw with the actual ether.
It could donate an electron to this bond right over here, in
which case, you would have a resonance structure
that looks like this.
And if it donates an electron to this carbon over here, then
an electron can be taken away from the carbon and given back
to that oxygen.
So that would give us a resonance structure that would
look like this.
That guy now has a negative charge.
We now have a double bond to this oxygen.
it still has another bond to the other acyl
group, just like that.
And now this oxygen gave away an electron, so it has a
positive charge.
So it seems like a very similar situation to what we
saw with an ether.
But there's another resonance structure here.
You could also have a situation where instead of the
electron being donated to this carbon bond and that
happening, you could have a situation like this, where the
electron gets donated to that carbon bond and then this
electron gets taken back by that oxygen, so you would have
this situation.
You would have a situation where this acyl group still
looks the same bonded to this oxygen, but now we have a
double bond over here.
This guy took away an electron.
So one of the bonds in the double bonds goes away.
It now has a negative charge, and then you have the rest of
the molecule.
So you actually have these two resonance structures.
And, of course, this is now a positive charge since it gave
away electron.
So you might say, hey, more resonance
structures, more stability.
But the key here is to realize that both resonance structures
are dependent from the same oxygen.
They essentially have to share this oxygen's electrons.
So each one of these individually is less likely to
occur than just what occurs with the ether.
You can kind of view it as both of these bonds have to
share what in the ether this one gets on its own.
And we even saw that this is still less likely to occur
than this over here.
So in this situation, in an anhydride, if one guy's
getting the double bond, the other guy's-- if there's a
resonance structure on one side of the anhydride, the
other side is still reactive.
If there's a resonance structure on the left side,
then the right side is still reactive, so we'll call this
less stable.
This right here is less stable.
Then finally, you have your acetyl chloride.
And acetyl chloride, there really is no resonance
structure here.
Chlorine is so electronegative that it is unlikely to give
away an electron.
It is sitting pretty with eight electrons.
That's actually true from these other
characters right here.
But chlorine is very, very unlikely to contribute a
resonance structure here.
So this gets no stability, so this is the least stable of
the carboxylic acid derivatives that
we're looking at.
Now, why am I even bothering with all of this hierarchy of
stability for carboxylic acid derivatives?
And I'm bothering with it because we know-- or we don't
know quite yet, but I've already shown you some
mechanisms that can take us from a carboxylic acid to an
ether or carboxylic acid to an acyl halide.
And, in general, you can go between all of these and a
carboxylic acid.
But since we know their relative stabilities, we know
that if you start with an acetyl chloride, you're much
more likely to go to an acetamide if you have the
proper ingredients in there.
If you have some amides floating around than the other
way around.
You're much more likely to go from that to that, because
this is much less stable than that, then you are to go from
acetamide to acetyl chloride.
Likewise, you're much more a likely to go from a carboxylic
acid to-- let me put it this way.
You're much more likely to go from a carboxylic acid to an
acetamide, and I haven't drawn the carboxylic acid here, but
this has better resonance than even its original carboxylic
acid than the other way around.
Or you're much more likely to go from an
anhydride to an ether.
So that's why I'm doing this hierarchy.
You're much more likely to go from something on the right to
something on the left.
And we'll explore some of those mechanisms in the next
few videos.

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Relative Stability of Amides Esters Anhydrides and Acyl Chlorides

Relative Stability of Amides Esters Anhydrides and Acyl Chlorides