Proton NMR & Analyzing NMR Spec - What to Do?

  • Thread starter Thread starter Moogie
  • Start date Start date
  • Tags Tags
    Nmr Spectroscopy
AI Thread Summary
Protons that are hydrogen-bonded to functional groups such as -OH, -COOH, and -NH2 may not appear in proton NMR spectra due to exchange with protic solvents, which can lead to discrepancies in integration values compared to the empirical formula. In this case, the empirical formula C9H8O2 suggests the presence of a carboxylic acid or alcohol. Additionally, factors such as different T1 relaxation times among proton types, improper pulse angles in multi-pulse experiments, and phase correction issues can affect integration accuracy. For more precise results, conducting a single pulse experiment with a non-exchangeable solvent like CDCl3 and a 45-degree pulse is recommended.
Moogie
Messages
167
Reaction score
1
Hi

Are there any protons that do not show up on proton NMR as I am analysing an NMR spec (of a known molecule but I don't know what it is!) and I can't get my integration to equal the number of Hs in the empirical formula of the molecule

Many thahks
 
Chemistry news on Phys.org
If a proton is hydrogen bonded to another molecule (-OH-groups, COOH, even -NH2) it may not show up on the spectrum.

Check for example the spectra of ethanol, acetic acid and ethyl amine.

What is the empirical formula?
 
Many times, if you are using protic solvents, acidic protons, like the proton is -OH, -COOH, and -NH2 groups will not show up in proton NMRs because they are being exchanged with the solvent.
 
It must be some kind of alcohol or acid then. I didnt know some protons didn't show up. I'll be ok now :) The empirical formula is C9H8O2. Perhaps some sort of carboxylic acid from the 2 x oxygen.
 
depending on the number of missing protons, it might be a carboxylic acid, ether alcohol or diol. It might even be a hydroperoxide, who knows?
 
Moogie said:
It must be some kind of alcohol or acid then. I didnt know some protons didn't show up. I'll be ok now :) The empirical formula is C9H8O2. Perhaps some sort of carboxylic acid from the 2 x oxygen.

In addition to exhcangeable protons (protons alpha to a carbonyl haven't yet been mentioned) you can have other effects. If your sample has several proton types that have significantly different T1's you can saturate those with the longer T1's in a multi pulse experiment. If you use too large of a tip angle, that becomes problematic in multi pulse experiments. If the offset frequency is for some reason off to one side or the other, integrations are affected. I've seen bad phase correction affect integration for protons near the low and high sides of the spectrum.

If you want to get as accurate as you can, perform a single pulse experiment on a sample of 33% concentration using a non-exchangeable solvent like CDCl3. Use a 45 degree pulse.
 
I want to test a humidity sensor with one or more saturated salt solutions. The table salt that I have on hand contains one of two anticaking agents, calcium silicate or sodium aluminosilicate. Will the presence of either of these additives (or iodine for that matter) significantly affect the equilibrium humidity? I searched and all the how-to-do-it guides did not address this question. One research paper I found reported that at 1.5% w/w calcium silicate increased the deliquescent point by...
Back
Top