IR Spectroscopy — Transcript
Full transcript
- 0:00hey it's professor Dave, let's talk about IR spectroscopy
- 0:10a lot of times when we do chemistry we face a very big challenge and that is that we cannot see
- 0:14molecules, so we might do some chemical reaction, get a product, and we need some
- 0:19way to be sure that what we got is what we think it is because we can't
- 0:22we can't see the structure of the molecule so we haven't we have a number
- 0:26of techniques that fall under the umbrella term of spectroscopy.
- 0:30spectroscopy is the study of the interaction of light and matter and so
- 0:35there's a lot of forms of spectroscopy that we can use to gather data about
- 0:39what the structure of a molecule might be and so right now if you look at IR
- 0:43spectroscopy IR stands for infrared as in infrared light so what we're gonna do
- 0:48is say we do reaction we have some molecule, we wanna figure out what the molecule
- 0:52is, we irradiate the sample with infrared light, that light is
- 0:58going to interact in some way with the compounds in the sample and
- 1:01then it'll eventually reach a detector so some light will be absorbed by the
- 1:05sample, some will not, some will pass through and this is information that we
- 1:09can use to figure out something about the structure of the molecule. the reason
- 1:13that we use infrared light is because different molecules, we already
- 1:17know that molecules move around, they have translational motion, we know
- 1:22that heat energy is converted into kinetic energy of motion so molecules
- 1:26that, say in a gas or even in a liquid are moving around with respect to one
- 1:31another, and through conformational analysis we also know that bonds are
- 1:35rotating all the time so there is rotational motion for all the all of the
- 1:39sigma bonds but chemical bonds are also doing other things. as it happens they
- 1:44can do these other things that occur specifically when they are
- 1:47irradiated with a very specific wavelength of infrared light. they can do
- 1:52something like a symmetric or asymmetric stretch so let's say my body is the
- 1:56central atom and these are two atoms that it is bound to and so my arms are
- 2:01covalent bonds and so this would be a symmetric stretch, the covalent bonds
- 2:05can
- 2:06actually be contracting and expanding at a particular vibration depending on
- 2:12whether it has absorbed this particular photon of UV light. so this is a symmetric
- 2:16stretch this would be an asymmetric stretch and we can also have a
- 2:20symmetric bend or asymmetric bend in plane so that would look like this, this
- 2:24would be symmetric or we could have asymmetric and we can actually have
- 2:28twisting, we can have it like this which would be symmetric or it would be, I can't
- 2:32even do it, it's very difficult to do but the point is we have all of these
- 2:35different kinds of vibrational motions happening in a molecule and they occur
- 2:40at very particular energies so they will occur when a wavelength of very specific
- 2:47infrared light is absorbed and it will vary depending on the functional group
- 2:51so the identity of these atoms will affect the photon absorption so this is
- 2:58information that we're going to use to generate an IR spectrum, so let's look
- 3:03at what that looks like right now
- 3:07ok so what I've done here is i've drawn a sample IR spectrum so let's take a look at what
- 3:12these look like and try to understand what we can use them for. so let's look at the
- 3:16axes, first on the bottom here we have the wavenumber. the wavenumber is
- 3:20telling us about the very particular energy of infrared light, so infrared
- 3:25light is a certain band, it's a certain part of the electromagnetic
- 3:28spectrum all the way from this wavelength to this wavelength so there
- 3:32are many energies of infrared light in between and so we're irradiating our
- 3:35sample with all of this infrared light of all of these different wavelengths
- 3:39and so the wave numbers here are the way we differentiate between those
- 3:42individual energies of IR radiation. on this axis we have the transmittance or
- 3:49the percentage of that particular wavelength or that particular wavenumber
- 3:53rather that reaches the detector so if we get, if we have information at a
- 3:59hundred percent or near a hundred percent transmittance that means that
- 4:04IR light that corresponds to that wave number is all getting through, it's all
- 4:08getting through the sample it is not being absorbed by the sample it's gonna
- 4:12make it to the detector and then we have peaks here where we have information so
- 4:16let's look at this wave number
- 4:17right here whatever is going on with with IR light of this particular
- 4:21wavenumber it is not making it to the detector we can see that it has a very
- 4:26low percent transmittance and if it is not making it to the detector it is
- 4:31being absorbed by something in the sample so there is a particular
- 4:34functional group in the molecule that is in the sample that absorbs IR light of
- 4:39that wavenumber and that is information that tells us about what
- 4:43kind of bonds are in that compound. so looking across here we can see
- 4:49here's some important data, here's some important data
- 4:53we should note that this region here around 1500 and below is called the
- 4:57fingerprint region, there's very delicate information there, very
- 5:02complicated to analyze and it goes beyond the scope of this tutorial so we
- 5:05won't talk about the fingerprint fingerprint region right now but what we want
- 5:09to understand is that we have tables, now i've only drawn, only written three
- 5:14things up here but there's long tables of every functional group that we can
- 5:17imagine in a molecule and we can talk about the particular wave number of IR
- 5:23light that is absorbed by that functional group so for example we have
- 5:27the OH sigma bond right here
- 5:31the OH stretch occurs at this wave number so if that oxygen hydrogen covalent bond
- 5:38absorbs infrared light of that particular wavenumber it will begin to stretch like
- 5:43this and if it does, if it is irradiated with light of that wave number it is
- 5:48being absorbed which means it does not get to the detector and that's why we
- 5:53see something like this so we call this the OH stretch and so what this means in
- 5:59terms of data that we can interpret from an IR spectrum if there is an OH stretch
- 6:04there is an 0H group in the molecule that means there is a hydroxyl group
- 6:09somewhere in the molecule. we can look at the spectrum and be very confident that
- 6:13there is a hydroxyl group in this molecule. now there's a couple others
- 6:16we will just look at the three most basic ones. the next one is called the
- 6:20saturated CH stretch so the saturated CH stretch means that there is fully
- 6:27saturated carbon bound to hydrogen meaning this is not an sp2 carbon, is not
- 6:33an SP carbon, this is a carbon this is a fully saturated carbon so it
- 6:39has the maximum bonds to other carbon and hydrogen and so this carbon-hydrogen
- 6:44bond if it absorbs IR light of that wavenumber it will begin to stretch and
- 6:48so it's not all making it to the detector and so that's there and most
- 6:53organic compounds will give you a saturated CH stretch because most
- 6:58organic compounds have some saturated carbon-hydrogen bond in it
- 7:02okay and then lastly let's look at the carbonyl stretch. now this may vary
- 7:08depending on whether it is a carbonyl from an aldehyde, ketone, ester, or
- 7:12what have you
- 7:13but it will generally occur somewhere in this region and it will look somewhat
- 7:17like this and so if we have that stretch we know that there is a carbonyl. now
- 7:23the last thing we wanna point out, a very common error is that people will say well
- 7:27there's a saturated CH stretch, that's the only functional
- 7:31group present, or they will say there's an OH stretch so there can't be some
- 7:36other functional group, all we are trying to understand is that every functional
- 7:40group in the molecule will be represented on the IR spectrum so let's
- 7:44just say hypothetically we had a molecule that gave us this spectrum, we
- 7:49would know that there is saturated carbon-hydrogen bonds, we know that
- 7:52there's a hydroxyl group, and we know that there's a carbonyl of some kind
- 7:55so that could look like anything, it doesn't tell us the precise structure of
- 7:59the molecule, but it could look, say, like this it could have a hydroxyl there and it could
- 8:05have a carbonyl there we're not sure, it's not telling us the precise
- 8:09structure, but the reason this could be useful is that let's say we
- 8:14do some reaction and maybe even know the empirical formula of our product and we
- 8:19know that
- 8:19we know that our
- 8:21compound had as an oxygen atom. well the reason IR would be useful for that
- 8:27is we would say: what kind of oxygen is it? is it a hydroxyl oxygen? is that an
- 8:32ether oxygen? is it a carbonyl oxygen? and we might get an IR spectrum and know just
- 8:38from that at least what kind of functional group the oxygen is
- 8:41participating in. if we saw an OH stretch we would say that oxygen must be
- 8:45a hydroxyl oxygen. if that was not present we would know that it is not
- 8:49that, it is not a hydroxyl oxygen, so the main thing that we want to get from this
- 8:54very basic introduction to IR spectroscopy is that functional groups
- 8:59that absorb IR light at specific wave numbers will provide very specific peaks
- 9:05not only are they occurring at specific wave numbers but they have
- 9:08characteristic shapes, the OH has a nice curvy dip like this, the carbonyl is thin and long
- 9:13and so we can take an IR spectrum and we can know roughly what kind of functional groups are in a molecule
- 9:21thanks for watching guys, subscribe to my
- 9:23channel for more tutorials and as always feel free to email me
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