Integration of H NMR Signals - Spectroscopy - Organic Chemistry
This organic chemistry video discusses the integration of H-NMR signals in NMR spectroscopy. It relates the area under the curve with the height of the integral trace to the relative number of protons in the molecule.
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Many thanks for the information. I had one question? How about in the formula below? N-morpholinebutadiene-2,3
I'm confused about your example at
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we thank you for your presentations. but just one observation is that the CH3 must be more downnfied than the (CH3)2 since it is nearer to the oxygen which would deshield it, hence, less effective magnetic field, resulting in smaller chemical shift position.
Please teach kolbe's and Reimer Tiemman reaction
Hello sir ! Thank you for the videos about NMR. I am learning quite a lot. In the second example, I understand it's obvious that the protons B produce the second taller signal. But I do not understand how the protons B which are connected to a primary carbone far from the carbonyl function are more deshielded than protons C closer to the carbonyl function.
nice................1st view and 1st like
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So there are no doublets, triplets,etc when considering integration?
My chemistry professor said the number of hydrogens and height of the peak are not related at all, that it's related to the area under the peak. Which is it? I'm so confused...