Let's try to come up with the reaction of when we have this
molecule right here reacting with sodium methoxide in a
methanol solution, or with methanol as the solvent.
Just so we get a little practice with naming, let's
see, this is one, two, three, four carbons.
So it has but- as a prefix and no double bond or triple
bonds, so it's butane.
And we have a chloro group here.
So if we start numbering at the side
closest to it, one, two.
So it's 2-chlorobutane.
Let's think about what might happen here.
The first thing-- let me just redraw the
molecule right there.
The first thing you need to realize is this sodium
methoxide is a salt.
When it's not dissolved, it's made up of a
positive sodium cation.
Let me draw them right here.
It's a positive sodium cation and a
negative methoxide anion.
Let me draw the methoxide part right here.
It normally would have just two pairs, but now we have
three pairs here.
The oxygen has an extra electron.
Actually, let me draw another electron
as the extra electron.
This'll be useful for our mechanism.
It could be any of them.
The oxygen has an extra electron.
It has a negative charge.
In solid form, when they're not dissolved, they had formed
an ionic bond and they form a crystal-like structure.
It's a salt, but when you dissolve it in something, in a
solution, in this case, we have methanol as the solution,
they will disassociate from each other.
And what you have right here is this methoxide right here.
This is a very, very, very strong base.
This right here is a strong base.
And if you use the Lewis definition of a base, that
means it really, really, really wants to give away this
electron to something else.
If you use the Bronsted-Lowry definition, this means that it
really, really, really wants to take a proton off of
something else.
In this situation, that is exactly what it will do.
I'll actually give you the most likely reaction to occur
here, and we'll talk about other reactions, and why this
is the most likely reaction in future videos.
So it wants to nab a proton.
It is a strong base.
It wants to give away this electron.
Let's say that it gives away this electron to this hydrogen
right over here.
Now, this hydrogen already had an electron.
If it's getting an electron from the methoxide anion, the
methoxide base, then it can give away its electron to the
rest of the molecule.
It can give away this electron to the rest of the molecule.
Now, carbon won't need the electron.
Carbon doesn't want to have a negative charge.
Maybe simultaneously that electron goes to that carbon
right over there.
But once again, this carbon doesn't want it.
It already has four bonds, but what we see is we have this
chloro here.
This is a highly electronegative group.
The chlorine is very electronegative, so the whole
time, the chlorine was already tugging on this
electron right here.
Now, all of a sudden, it's all happening simultaneously, when
an electron becomes available to this carbon, this carbon
doesn't need this electron anymore.
The chlorine already wanted it, so now the chlorine can
take the electron.
And just like that, in exactly one step, let's think about
what happened.
If all of these simultaneous reactions occurred, what are
we left with?
Let me redraw my two chlorobutanes.
I'm going to have to change it now.
So now, the chlorine has disappeared.
So we clear it.
That's disappeared.
The chlorine has now left.
This chlorine is now up here.
It has left.
It had this electron right over there, which is right
over there.
The other electron it was paired with that was forming a
bond with is now also on the chlorine.
It becomes a chloride anion.
Let me draw the rest of the valence electrons.
One, two, three, four, five, six, and it has the seventh
one right here.
One, two, three, four, five, six, seven, eight, so it now
has a negative charge.
This electron up here-- let me clear this part out as well.
Now, this electron right here, this magenta electron, this is
now given to this carbon.
Let me draw it here.
That magenta electron is now given to that carbon.
And if we look at the other end, the one that it was
paired with, that it was bonded with, it still is
bonded with it, so that green electron is now still on that
carbon and now they are bonded.
Now, they're forming a double bond.
This all of the sudden has become an alkene and now the
methoxide took the hydrogen.
Let me redraw the methoxide.
OCH3, the oxygen had one, two, three, four, five.
It had six.
Actually, it had seven valence electrons, one with the carbon
and then all of these six unpaired ones.
Neutral oxygen has six.
But now it gave one of them away to a hydrogen.
It gave that green electron there to the hydrogen-- I'll
make this hydrogen the same color-- to this hydrogen right
over here, so now this hydrogen is
now bonded with it.
So what are we left with?
We have a chloride anion, so this is chloride.
We now have methanol.
This was a strong base.
Now it has become its conjugate acid.
So now we have methanol, which is the same as the solvent, so
it's now mixed in.
And now we're left off with one, two,
three, four, still four.
We still have four carbons, but now it's an alkene.
We have a double bond, so we could call this but-2-ene, or
sometimes called 2-butene.
Let's think about what happened here.
It all happened simultaneously.
Both reactants were present.
There was actually only one step so this is the
rate-determining step.
If we would try to name it, it would probably
have a 2 in it someplace.
And something got eliminated.
The chloride, or I guess you could call it the chloro
group, got eliminated.
It left.
It was a leaving group in this situation.
So this was eliminated, and this type of reaction where
something is eliminated and both of the reactants are
participating in the rate-determining step, and we
only had one step here so that was the rate-determining step,
is called an E2 reaction.
And once again, E stands for elimination.
And the 2 stands for that both reactants were involved in the
rate-determining step.
We had one reactant and two reactants.
They were both involved with the rate-determining step.
E2, just like Sn2.
It's obviously not the same reaction, but in Sn2, we had
substitution.
The leaving group left, nucleophile came.
It was substitution using a nucleophile so that's
the S and the n.
And then the 2 was we had both reactants.
It was all happening simultaneously.
I'll leave you there.
We're going to go into more detail on the different types
of each reactions, which ones are favored, and then we'll
talk a little bit about E1.
You could maybe guess what that's going to be based on
our experience with Sn2 and Sn1.