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Deuterium has a nuclear spin of 1; causes the C-13 signal to be split into a triplet at 77.0 ppm

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Q: Why chloroform appeared as triplet in carbon 13 nmr?
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Why does a triplet occurs in C 13 nmr spectra with CDCl3?

In this case, carbon nuclei can couple with deutrium one and the spin quantum no. (I) of deutrium is 1. So according to the famous formula to find the multiplicity of a signal (2nI+1) in NMR, it comes out to be 3 i.e. triplet.


Why does a triplet occurs in C-13 nmr spectra with CDCl3?

In this case, carbon nuclei can couple with deutrium one and the spin quantum no. (I) of deutrium is 1. So according to the famous formula to find the multiplicity of a signal (2nI+1) in NMR, it comes out to be 3 i.e. triplet.


How do you calculate nmr j value for triplet and for multiple?

for a triplet. You have to take the (difference between the middle and one of the outer frequencies)* the frequency in MHZ


How will you distinguish between chloroform and carbon tetrachloride?

Well, they smell different, but boiling point, index of refraction, NMR or IR spectrum would be safer and more reliable methods.


In chemistry for a proton NMR what does an apparent triplet mean?

As far as I'm aware, it means that it looks like a triplet, but you don't expect a triplet. It's "really" a doublet of doublets, but the two coupling constants are too similar, so it looks like a triplet, as the two inner peaks merge.


Is chloroform a legal substance and if so where can you purchase it?

you will have to order it from a chemical supply catalog. It is legal, its used all the time as a solvent in analysis with NMR.


What is the primary advantage of 3D-NMR over 2D-NMR?

One more D.It's difficult to answer this question exactly, since it's not always necessarily true that 3D NMR is better than 2D NMR (or even than 1D NMR). It really depends on what information you're looking for. In fact, sometimes information that theoretically couldbe used to add an extra dimension is intentionally supressed (example: carbon-13 CP-MAS, where the proton spins are deliberately blasted to decouple them from the carbon nuclei), because the spectroscopist is not interested in that.


What are the application of NMR?

The main applications of NMR stereoscopy are the elucidation of the carbon-hydrogen backbone of organic compounds and the determination of the relative stereochemistry of the same molecule. See the link below for more details.


What has the author LeRoy F Johnson written?

LeRoy F. Johnson has written: 'Carbon-13 NMR spectra' -- subject(s): Carbon, Isotopes, Nuclear magnetic resonance spectroscopy, Spectra 'Interpretation of NMR spectra' -- subject(s): Nuclear magnetic resonance


In the H NMR spectrum why does 1 2-dichloroethane show up as a singlet and not a triplet?

The molecule is symmetric so all protons are equivilent. Equivilent protons cannot couple with each other, so the spectrum is a singlet.


What is the difference between NMR and FT- NMR instrumentation?

NMR Spectroscopy Use molecule Structure FT NMR Use Different No. of mass Structure


What is the difference between proton and 13C for NMR?

Proton is an elementary particle (hydrogen nucleus) with the mass of approx. 1. Carbon-13 is a carbon natural isotope with the mass of approx. 13.