If we look at methane, we have four equivalent protons. So we would expect one signal on an NMR spectrum. And here's the signal for the protons on methane. So this signal occurs at approximately one part per million. And remember from the first few videos on proton NMR, what that signal is talking about.
It's talking about the energy difference between the alpha between the alpha and the beta spin states. So this is the alpha spin state and this is the beta spin state. There's an energy difference between those two spin states, and this energy difference corresponds to a frequency because E is equal to h nu.
And the energy difference also corresponds to the effective magnetic field felt by a proton. So if I draw in a magnetic field here, so the effective magnetic field controls the energy difference. So let's think about this.
If I have a certain effective magnetic field, I get a certain difference in energy between the alpha and the beta spin states. The energy corresponds to a frequency that's absorbed, and so this, this signal is a certain frequency. Alright, we said before this was a lower frequency, this is a lower frequency signal right here. So this is a lower frequency signal. And in an earlier video we talked about how to Compare frequency to chemical shift.
So a low frequency gives a low chemical shift. So one is a low chemical shift here. And so the protons in methane are shielded compared to the protons in chloromethane.
So let's look at chloromethane next down here. So for chloromethane we have three equivalent protons, so one signal on our NMR spectrum. and this signal occurs just past three, so approximately 3.1 parts per million.
And let's see if we can understand why this occurs. So we now have an electronegative atom, right? Chlorine is much more electronegative than carbon, so chlorine is going to withdraw some electron density.
And so the chlorine gets partially negative, we give the carbon partial positive here. So the chlorine's withdrawing electron density from these protons. So these protons are deshielded from the applied magnetic field.
Alright, so here we have deshielded protons. Alright, so deshielding protons, if the protons are deshielded from the applied magnetic field, that means those protons experience a greater effective magnetic field. So let me go ahead and draw this in.
I'm just gonna exaggerate to get the point across. So a greater effective magnetic field for a proton. means a greater difference in energy between your alpha and your beta spin states.
So alpha and beta spin states here. Now, since we have a deshielded proton, we have a greater difference in energy between our spin states, and energy corresponds to frequency. So a greater effective magnetic field means a greater energy difference, which means a larger frequency, so a higher frequency absorbed.
And so this, This would be a higher frequency compared to the previous example. So everything is relative here. So a higher frequency signal compared to the protons in methane.
And therefore, we get a higher value for the chemical shift. So let's just sum this up really quickly. So a shielded, shielded protons are going to give you a lower frequency signal and therefore a lower value for the chemical shift.
A deshielded proton is gonna give you a higher frequency signal and a higher chemical shift. Alright, so once again, just comparing these two things, that's what electronegativity does, right? So the more, here we have an electronegative atom that's deshielding the protons, giving a higher chemical shift.
So that's the idea, and let's apply this to a chart that has a bunch of different functional groups here, and let's think about the different chemical shifts for protons in different environments. Alright, so we just said, that if you deshield a proton, you're gonna get a higher frequency signal and therefore a higher chemical shift, and this is called downfield. So the left side of this NMR spectrum, these are more deshielded protons. To the right side of the NMR spectrum, we're talking about more shielded protons, therefore a lower frequency signal, therefore a lower chemical shift, and you could use the older term upfield if you wanted to as well.
So we just talked about methane. So we're talking about an alkane type environment here. So the proton on a carbon in an alkane type environment, the chemical shift, this is a shielded proton. So we would expect a low frequency signal or a low chemical shift.
So somewhere in the range of 0.5 to 2 is where we would expect the signal for a proton in an alkane type environment. So somewhere in that range. Alright, so those are more shielded.
Next we talked about chloromethods. In chloromethane we had an electronegative atom on a carbon that was bonded to our proton. So that's this situation. Let me use yellow for this.
So here we have y as an electronegative atom. So you could think about something like chlorine or fluorine, so a halogen. Or you could think about oxygen, also electronegative.
So if y is an electronegative atom, y withdraws electron density from this carbon. and that deshields this proton that's directly on that carbon. So deshielding the proton gives you a higher chemical shift, and so you'd expect this shift to be approximately 2.5 to 4.5. So if you see a signal in 2.5 to 4.5 range, it could be a proton that's on a carbon that's directly bonded to an electronegative atom, like a halogen or like oxygen.
Alright, so in between those two examples, So the signal for this proton right here, this proton would show up approximately two to 2.5. And so this proton is directly bonded to a carbon, but this carbon is not directly bonded to an electronegative atom. But it is bonded to this carbon, which is a carbonyl here. So this oxygen is more electronegative.
This oxygen withdraws some electron density. But not quite as much as in this example with this electronegative atom directly on this carbon. And so the signal, the chemical shift is in between here.
So a proton that's on a carbon that's next to a carbonyl, look for that approximately two to 2.5. Again, all of these are just approximate ranges here. So I tried to give nice, easy numbers to remember.
Next let's look at the proton on alcohol, so right here. Well, alcohols have hydrogen bonding, and hydrogen bonding has a deshielding effect. So increased hydrogen bonding, increased deshielding.
The problem is the amount of hydrogen bonding depends on things like concentration and temperature, and since those things can vary, you get different amounts of hydrogen bonding, you get different amounts of deshielding. you get a different range, a pretty broad range here for your possible signal. So approximately two to five for the signal on an alcohol.
But it might not even be in that range. So just think about two to five for the proton on an alcohol as an approximate region. Next, let's look at the proton on a double bond here. So proton bonded to a carbon. a proton on a double bond, the shift is approximately 4.5 to 6.5.
So let's see if we can understand why. One way to think about it is using electronegativity. And so if we think about this carbon here, this carbon is sp2 hybridized. And if we compare that carbon to this carbon, this carbon is sp3 hybridized.
Remember from hybridization videos that an sp2 hybrid orbital has more S character than an sp3 hybridized orbital. Therefore, the electrons are held closer to the nucleus. So you can say that an sp2 hybridized carbon is more electronegative than an sp3 hybridized carbon.
So if you want to think about it that way, that's one way to think about it. And so this sp2 hybridized carbon is withdrawing more electron density from this proton. Let me use a different color here. So this sp2 hybridized carbon is withdrawing more electron density, deshielding this proton, and giving you a higher chemical shift than for a proton bonded to an sp3 hybridized carbon.
So that's one way to explain this, but it doesn't, that line of reasoning isn't exactly, that doesn't hold up completely, because if we next look at a proton on a triple bond here, so if I draw a triple bond in this proton right here, So you might think, okay, well, this carbon is sp hybridized. And I know that sp hybridized carbon, an sp hybridized orbital has even more s character than an sp2 hybridized orbital. So therefore, you could think about an sp hybridized carbon being more electronegative, and these electrons are closer to this carbon.
And so you might think, oh, that's going to deshield. That's going to deshield this proton, and we would expect a signal that's an even higher chemical shift than for this proton. And that's not what we observe. So the proton on a triple bond, actually, this shows up somewhere in this range, so somewhere around two to 2.5 approximately. And so it's not just electronegativity that you have to think about.
So there's another effect. that's causing the chemical shift for this proton that we'll talk about in the next video. And it's the same thing, it's actually the same thing for the proton on a benzene ring. So we'll save that discussion for the next video.
So we'll talk about this and we'll talk about this in the next video. If we move on to an aldehyde, so for an aldehyde we have this carbonyl here. The oxygen's withdrawing electron density away from the proton on the aldehyde. And so it's deshielding that proton, right? Therefore we'd expect the signal for that proton to occur at a higher chemical shift, so somewhere around nine to 10 is where we'd expect the shift for this proton.
Finally, let's look at a carboxylic acid. So the signal for this proton, approximately 10 to 12. So once again we have this carbonyl here withdrawing electron density. We have another oxygen here withdrawing some electron density.
So you could think about electronegativity effects. You could also think about resonance effects. And you could also think about, there's some hydrogen bonding effects. There's all kinds of things going on here with the carboxylic acid.
And pretty much, if you're just looking in the 10 to 12 region and you see a signal, think the proton on a carboxylic acid.