- Proton nuclear magnetic resonance questions
- Magnetic resonance imaging (MRI)
- Introduction to proton NMR
- Nuclear shielding
- Chemical equivalence
- Chemical shift
- Electronegativity and chemical shift
- Diamagnetic anisotropy
- Spin-spin splitting (coupling)
- Multiplicity: n + 1 rule
- Coupling constant
- Complex splitting
- Hydrogen deficiency index
- Proton NMR practice 1
- Proton NMR practice 2
- Proton NMR practice 3
Predicting splitting patterns based on the molecular structure. Finding coupling constants from the peaks in a multiplet, and using roofing to figure out which protons are splitting each other. Created by Jay.
Want to join the conversation?
- At2:43, how do you know that the red proton is attributed to the peak with the lower chemical shift than the blue proton which has a peak with a higher chemical shift?(11 votes)
- I'm not entirely sure, but I think that this is the case because the blue proton is closer to the OSi(Me)3 group which is electronegative, thus it is more deshielded and experiences a higher magnetic field and thus a higher chemical shift. It is relatively closer to the OSi(Me)3 group because it is cis to it rather than the other hydrogen which is trans.(13 votes)
- At5:36: Did you determine the distance between the peaks by adding the two peak numbers together, so 4 + 3 = 7? Or was it determined in another way with a scope outside of this video?(4 votes)
- Coupling constants are values that must be memorized (or will be provided) and depend on the relative position of protons and their near neighbors. These are independent of the number of peaks, and 3+4=7 was just a coincedence(13 votes)
- I don't understand how the two hydrogens are chemically different. Can someone explain this to me more in depth? Is it only when there is a double bond?(1 vote)
- No, it's not only when there is a double bond.
Two hydrogens are chemically different if, when you replace them separately with an X group, to get a different compound.
In CH₃CH₂CH₃, replacing an H with X on C1 or C3 gives CH₃CH₂CH₂X, so those six H atoms are chemically identical
Replacing one of the H atoms on C2 gives CH₃CHXCH₃, so those two H atoms are chemically identical but chemically different from the other six H atoms.(10 votes)
- so if there was rotation about the double bond, the protons would be equivalent?(2 votes)
why we use Hz as a unit of coupling constant ? this video says that it is because of different spectrometer's frequency, but even with different spectrometer frequency we still can calculate the same chemical shift δ right ?(2 votes)
- We use δ for chemical shift because the frequency varies with spectrometer frequency.
We use Hz for coupling constant because it is a constant.
If J = 7 Hz on one spectrometer, it is the same on every spectrometer.(4 votes)
is there any way to determine the coupling constant from the spectrum? or has it to be given?
could you please explain me what is the difference between the spectrum of first order and higher ones?
Thank you :)(3 votes)
- Does the molecule Chloroethyl acetate show only two signals on a proton-NMR spectra? Or should it be three signals when the protons on the first carbon are also considered?(1 vote)
- I think the CH2 next to the Cl will have a peak, but it will only be a singlet since it has no hydrogen neighbors(2 votes)
- What is an NMR operating frequency? We send short pulses of different frequencies keeping the magnetic field constant, so why is there any specific frequency, say 300 MHz, associated with an NMR machine?(1 vote)
- [Voiceover] If you look at the red and blue protons, they're both attached to this carbon, and if we see this double bond here, we have these different groups attached to this double bond, and since there's no rotation around the double bond, the red and the blue protons are locked into different environments, therefore, they are NOT chemically equivalent, and since those protons are not equivalent, they can couple together, and since this is occurring on the same carbon, we call this geminal coupling, so geminal coupling here, so geminal, referring to the fact that both protons are on the same carbon, and coupling can occur, so those protons are close enough where they can affect each other. So let's think about first, the NMR spectrum with no coupling, so we would expect one signal for the blue proton, and one signal for the red proton. So here's the spectrum with no coupling, but we know that the red proton's magnetic moment can align either with the external magnetic field, or against the external magnetic field, and that causes the signal for the blue proton to be split into two, so if I go down here, so we actually see a doublet for the signal for the blue proton. Same thing for the blue proton. The magnetic moment can be aligned either with the external magnetic field, or against it, and that splits the signal for the red proton into a doublet, so two peaks for the signal for the red proton. I went into much more detail about this in the spin-spin splitting/spin-spin coupling video. In this video, we're more concerned with the idea of the coupling constant, and the coupling constant refers to the distance between the peaks of a signal. So if you think about the distance between the two peaks of this signal, that is the coupling constant, and the coupling constant is the same for both of these signals, because these protons are splitting each other. They are coupled together. The coupling constant is measured in Hertz, so it turns out to be 1.4 Hz, and if it's 1.4 Hz for this one, it must be 1.4 Hz for this one, because those protons are coupled together. The reason why we use Hertz, is because it's the same coupling constant no matter what NMR spectrometer you're using, so it doesn't matter what the operating frequency is. You're going to get the same coupling constant. Alright, if we look at the actual NMR spectrums, over here is a zoom-in of the actual NMR spectrum. The signal for the red proton is right here, and the signal for the blue proton is over here. So, when I looked at the spectrum with interaction, the spectrum with coupling between the protons, we just assumed that the heights of these two peaks were the same, but if I look at the actual NMR spectrum, they're not quite the same. So this one right here is a little bit higher, and if you draw an arrow pointing towards the higher peak, that arrow points towards the signal of the proton that's causing the splitting. So that arrow is pointing to the right, and that's where we find the signal for the red proton, which is causing the splitting of the blue proton. So the doublet points towards the proton with which it is coupled, and the same thing for this signal. So this peak's a little bit higher, so we draw an arrow pointing towards the higher peak, and so the doublet points toward the proton with which IT is coupled, and so you get this situation where you get these doublets with like a roof over their head. So if you could imagine this roof over them like that. So, sometimes you'll see this on an NMR spectrum, and if you think about that they're pointing towards the proton with which it is coupled, sometimes it can help you when you're trying to understand what's going on in your NMR spectrum. Alright, let's look at another example for a coupling constant, so let's look at this molecule, and let's focus on the ethyl group. So, over here, this carbon has two protons, so we expect one signal for those protons, and then over here, this carbon has three protons, so we would expect another signal for these protons. Let's focus in on the protons in blue. So how many neighboring protons do we have? Well, those protons in blue are attached to this carbon. The next-door carbon is this one. So how many neighbors? One, two, three, so three neighboring protons, so n is equal to three. I'm using the n plus one rule. We expect n plus one peaks, so three plus one is equal to four, so we would expect a signal with four peaks, so we would expect a quartet. So let me go ahead and draw that down here, so we would expect a quartet for that signal, so this is supposed to represent what you would see on an NMR spectrum. Next, let's do the protons in red here, so how many neighboring protons do they have? Well, they're all attached to this carbon, and the next-door carbon is here, and we have two protons on the next-door carbon, so we have two neighbors, so n is equal to two, and so we'd expect two plus one peaks, so three peaks, or a triplet. So let me see if I can draw in a triplet here. So this would be the signal for these protons. Since the red and the blue protons are splitting each other, the coupling constant is the same. So the distance between the peaks should be the same, so it turns out to be 7 Hz, so this distance should be 7 Hz, the same with this distance, so we just have to pretend like they're all equivalent here, and the same for this one, so a coupling constant of 7 Hz. Same for this signal. So this distance should be 7 Hz, and also for this one, so hopefully this just gives you an insight into the idea of a coupling constant, which you'll need, to understand more complex splitting, which we'll talk about in the next video.