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Let's remind ourselves a little
bit of what we already
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know about orbitals and I've
gone over this early on in the
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regular chemistry playlist.
Let's say that this is the
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nucleus of our atom, super
small, and around that we have
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our first orbital,
the 1s orbital.
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The 1s orbital, you can kind
of just view it as a cloud
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around the nucleus.
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So you have your 1s orbital and
it can fit two electrons,
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so the first electron will go
into the 1s orbital and then
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the second electron will also
go into the 1s orbital.
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For example, hydrogen has
only one electron, so it
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would go into 1s.
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Helium has one more,
so that will also
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go into the 1s orbital.
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After that is filled, then you
move onto the 2s orbital.
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The 2s orbital, you can view
it as a shell around the 1s
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orbital, and all of these, you
can't really view it in our
-
conventional way of thinking.
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You can kind of view it as a
probability cloud of where you
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might find the electrons.
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But for visualization purposes,
just imagine it's
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kind of a shell cloud around
the 1s orbital.
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So imagine that it's kind of
a fuzzy shell around the 1s
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orbital, so it's around the
1s orbital, and your next
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electron will go there.
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Then the fourth electron will
also go there, and I drew
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these arrows upward and downward
because the first
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electron that goes into the 1s
orbital has one spin and then
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the next electron to go into
1s orbital will have the
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opposite spin, and so they keep
pairing up in that way.
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They have opposite spins.
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Now, if we keep adding
electrons, now we move to the
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2p orbitals.
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Actually, you can view it as
there are three 2p orbitals
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and each of them can hold two
electrons, so it can hold a
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total of six electrons
in the 2p orbitals.
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Let me draw them for you just
so you can visualize it.
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So if we were to label our axis
here, so think in three
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dimensions.
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So imagine that that right
there is the x-axis.
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Let me do this in different
colors.
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Let's say that this right
here is our y-axis and
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then we have a z-axis.
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I'll do that in blue.
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Let's say we have a z-axis
just like that.
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You actually have a p orbital
that goes along
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each of those axes.
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So you could have your
two-- let me do
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it in the same color.
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So you have your 2p sub x
orbital, and so what that'll
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look like is a dumbbell shape
that's going in the
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x-direction.
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So let me try my best attempt
at drawing this.
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It's a dumbbell shape that goes
in the x-direction, in
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kind of both directions, and
it's actually symmetric.
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I'm drawing this end bigger than
that end so it looks like
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it's coming out at you a little
bit, but let me draw it
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a little bit better than that.
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I can do a better job.
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And maybe it comes
out like that.
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Remember, these are really just
probability clouds, but
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it's helpful to kind of
visualize them as maybe a
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little bit more things that we
would see in our world, but I
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think probability cloud is the
best way to think about it.
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So that is the 2px orbital,
and then I haven't talked
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about how they get filled yet,
but then you also have your
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2py orbital, which'll go in this
axis, but same idea, kind
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of a dumbbell shape in the
y-direction, going in both
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along the y-axis, going in that
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direction and in that direction.
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Then, of course, so let me do
this 2py, and then you also
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have your 2pz, and that goes
in the z-direction up like
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that and then downwards
like that.
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So when you keep adding
electrons, the first-- so far,
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we've added four electrons.
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If you add a fifth electron, you
would expect it to go into
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the 2px orbital right there.
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So even though this 2px orbital
can fit two electrons,
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the first one goes there.
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The very next one won't
go into that one.
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It actually wants to separate
itself within the p orbital,
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so the very next electron that
you add won't go into 2px,
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it'll go into 2py.
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And then the one after that
won't go into 2py or 2px,
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it'll go into 2pz.
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They try to separate
themselves.
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Then if you add another
electron, if you add-- let's
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see, we've added one, two,
three, four, five, six, seven.
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If you add an eighth electron,
that will then go into the 2px
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orbital, so the eighth electron
would go there, but
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it would have the
opposite spin.
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So this is just a little bit of
review with a little bit of
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visualization.
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Now, given what we just
reviewed, let's think about
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what's happening with carbon.
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Carbon has six electrons.
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Its electron configuration, it
is 1s2, two electrons in the
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1s orbital.
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Then 2s2, then 2p2, right?
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It only has two left,
because it has a
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total of six electrons.
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Two go here, then there,
then two are left
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to fill the p orbitals.
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If you go based on what we just
drew and what we just
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talked about here, what you
would expect for carbon-- let
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me just draw it out the
way I did this.
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So you have your 1s orbital,
your 2s orbital, and then you
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have your 2px orbital, your 2py
orbital, and then you have
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your 2pz orbital.
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If you just go straight from
the electron configuration,
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you would expect carbon, so the
1s orbital fills first, so
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that's our first electron,
our second
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electron, our third electron.
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Then we go to our 2s orbital,
That fills next, third
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electron, then fourth
electron.
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Then you would expect maybe
your fifth electron
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to go in the 2px.
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We could have said 2py or 2z.
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It just depends on how
you label the axis.
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But you would have your fifth
electron go into one of the p
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orbitals, and then you
would expect your
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sixth to go into another.
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So you would expect that
to be kind of the
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configuration for carbon.
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And if we were to draw it--
let me draw our axes.
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That is our y-axis and then
this is our x-axis.
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Let me draw it a little
bit better than that.
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So that is the x-axis and, of
course, you have your z-axis.
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You have to think in three
dimensions a little bit.
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Then you have your z-axis,
just like that.
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So first we fill the 1s orbital,
so if our nucleus is
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sitting here, our
1s orbital gets
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filled with two electrons.
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You can imagine that
as a little
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cloud around the nucleus.
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Then we fill the 2s orbital
and that would be a cloud
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around that, kind of a
shell around that.
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Then we would put one electron
in the 2px orbital, so one
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electron would start kind of
jumping around or moving
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around, depending how you want
to think about it, in that
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orbital over there, 2px.
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Then you'd have the next
electron jumping around or
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moving around in the 2py
orbital, so it would be moving
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around like this.
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If you went just off of this,
you would say, you know what?
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These guys, this guy over
here and that guy
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over there is lonely.
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He's looking for a opposite
spin partner.
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This would be the only places
that bonds would form.
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You would expect some type of
bonding to form with the
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x-orbitals or the y-orbitals.
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Now, that's what you would
expect if you just straight-up
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kind of stayed with this model
of how things fill and how
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orbitals look.
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The reality of carbon, and I
guess the simplest reality of
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carbon, is if you look at a
methane molecule, is very
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different than what you
would expect here.
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First of all, what you would
expect here is that carbon
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would probably-- maybe it
would form two bonds.
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But we know carbon forms four
bonds and it wants to pretend
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like it has eight electrons.
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Frankly, almost every atom wants
to pretend like it has
-
eight electrons.
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So in order for that to happen,
you have to think
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about a different reality.
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This isn't really what's
happening when carbon bonds,
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so not what happens
when carbon bonds.
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What's really happening when
carbon bonds, and this will
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kind of go into the discussion
of sp3 hybridization, but what
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you're going to see
is it's not that
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complicated of a topic.
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It sounds very daunting, but
it's actually pretty
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straightforward.
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What really happens when carbon
bonds, because it wants
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to form four bonds with things,
is its configuration,
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you could imagine, looks
more like this.
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So you have 1s.
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We have two electrons there.
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Then you have your 2s,
2px, 2py and 2pz.
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Now what you can imagine is it
wants to form four bonds.
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It has four electrons that are
willing to pair up with
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electrons from other
molecules.
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In the case of methane, that
other molecule is a hydrogen.
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So what you could imagine is
that the electrons actually--
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maybe the hydrogen brings this
electron right here into a
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higher energy state and
puts it into 2z.
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That's one way to
visualize it.
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So this other guy here maybe
ends up over there, and then
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these two guys are over
there and over there.
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Now, all of a sudden, it looks
like you have four lonely guys
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and they are ready to bond,
and that's actually more
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accurate of how carbon bonds.
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It likes to bond with
four other people.
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Now, it's a little bit arbitrary
which electron ends
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up in each of these things, and
even if you had this type
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of bonding, you would expect
things to bond along the x, y,
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and z axis.
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The reality is, the reality of
carbon, is that these four
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electrons in its second shell
don't look like they're in
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just-- the first one doesn't
look like it's just in the s
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orbital and then the p and y
and z for the other three.
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They all look like they're a
little bit in the s and a
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little bit in the p orbitals.
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Let me make that clear.
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So instead of this being a 2s,
what it really looks like for
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carbon is that this looks
like a 2sp3 orbital.
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This looks like a 2sp3 orbital,
that looks like a
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2sp3 orbital, that looks
like a 2sp3 orbital.
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They all look like they're kind
of in the same orbital.
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This special type of--
it sounds very fancy.
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This sp3 hybridized orbital,
what it actually looks like is
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something that's in between
an s and a p orbital.
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It has a 25% s nature
and a 75% p nature.
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You can imagine it as being a
mixture of these four things.
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That's the behavior
that carbon has.
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So when you mix them all,
instead of having an s
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orbital, so if this is
a nucleus and we do a
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cross-section, an s orbital
looks like that and the p
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orbital looks something like
that in cross-section.
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So this is a an s
and that is a p.
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When they get mixed up, the
orbital looks like this.
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An sp3 orbital looks something
like this.
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This is a hybridized
sp3 orbital.
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Hybrid just means a combination
of two things.
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A hybrid car is a combination
of gas and electric.
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A hybridized orbital is a
combination of s and p.
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Hybridized sp3 orbitals are the
orbitals when carbon bonds
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with things like hydrogen
or really when
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it bonds with anything.
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So if you looked at a molecule
of methane, and people talk
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about sp3 hybridized orbitals,
all they're saying is that you
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have a carbon in the center.
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Let's say that's the carbon
nucleus right there.
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And instead of having one s and
three p orbitals, it has
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four sp3 orbitals.
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So let me try my best at drawing
the four sp3 orbitals.
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Let's say this is the big lobe
that is kind of pointing near
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us, and then it has a small
lobe in the back.
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Then you have another one that
has a big lobe like that and a
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small lobe in the back.
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Then you have one that's going
back behind the page, so let
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me draw that.
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You can kind of imagine a
three-legged stool, and then
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its small lobe will come
out like that.
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And then you have one where
the big lobe is pointing
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straight up, and it has a
small lobe going down.
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You can imagine it as kind
of a three-legged stool.
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One of them is behind like
that and it's pointing
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straight up, So a three-legged
stool with something-- it's
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kind of like a tripod, I
guess is the best way
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to think about it.
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So that's the carbon nucleus
in the center and then you
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have the hydrogens, so that's
our carbon right there.
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Then you have your hydrogens.
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You have a hydrogen here.
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A hydrogen just has one electron
in the 1s orbital, so
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the hydrogen has a 1s orbital.
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You have a hydrogen here that
just has a 1s orbital.
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It has a hydrogen here,
1s orbital,
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hydrogen here, 1s orbital.
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So this is how the hydrogen
orbital and the carbon
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orbitals get mixed.
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The hydrogens 1s orbital bonds
with-- well, each of the
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hydrogen's 1s orbital bonds
with each of the
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carbon's sp3 orbitals.
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Just so you get a little bit
more notation, so when people
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talk about hybridized sp3
orbitals, all they're saying
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is, look, carbon doesn't bond.
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Once carbon-- this
right here is a
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molecule of methane, right?
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This is CH4, or methane, and it
doesn't bond like you would
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expect if you just want
with straight
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vanilla s and p orbitals.
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If you just went with straight
vanilla s and p orbitals, the
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bonds would form.
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Maybe the hydrogen might be
there and there, and if it had
-
four hydrogens, maybe there and
there, depending on how
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you want to think about it.
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But the reality is it doesn't
look like that.
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It looks more like a tripod.
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It has a tetrahedral shape.
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The best way that that can be
explained, I guess the shape
-
of the structure, is if you have
four equally-- four of
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the same types of orbital
shapes, and those four types
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of orbital shapes are hybrids
between s's and p's.
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One other piece of notation to
know, sometimes people think
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it's a very fancy term, but when
you have a bond between
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two molecules, where the
orbitals are kind of pointing
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at each other, so you can
imagine right here, this
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hydrogen orbital is pointing
in that direction.
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This sp3 orbital is pointing
that direction, and they're
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overlapping right around here.
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This is called a sigma bond,
where the overlap is along the
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same axis as if you connected
the two molecules.
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Over here, you connect the two
molecules, the overlap is on
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that same axis.
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This is the strongest form of
covalent bonds, and this'll be
-
a good basis for discussion
maybe in the next video when
-
we talk a little bit
about pi bonds.
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The big takeaway of this video
is to just understand what
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does it mean?
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What is an sp3 hybridized
orbital?
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Nothing fancy, just a
-
combination of s and p orbitals.
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It has 25% s character, 75% p
character, which makes sense.
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It's what exists when carbon
forms bonds, especially in the
-
case of methane.
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That's what describes it's
tetrahedral structure.
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That's why we have an angle
between the various branches
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of a 109.5 degrees, which some
teachers might want you know,
-
so it's useful to know.
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If you take this angle right
here, 109.5, that's the same
-
thing as that angle, or if you
were to go behind it, that
-
angle right there, 109.5
degrees, explained by sp3
-
hybridization.
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The bonds themselves
are sigma bonds.
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The overlap is along the axis
connecting the hydrogen.