Why is CDCl3 a Triplet?
Posted by naturalproductman on May 29, 2009
Ever wonder why when you’re taking a 13C NMR in deuterated chloroform and look at the solvent peak – there are three evenly spaced peaks with equal intensities?
The answer can be found in your good old sophmore organic chemistry textbook (*I recommend the Marc Loudon book) and/or a physical chemistry text. It turns out that 1H has a spin of 1/2 but 2H has a spin of 1. In the case of a proton (1H) the spin state will either be +1/2 or -1/2, and in the case of a deuterium (2H) the spin state will either be +1, 0 or -1. And since we’re not running the 13C NMR in a deuterium decoupled mode – we’ll see the splitting from deuterium onto the carbon. Because there are three states: +1, 0 and -1, then we’ll see the peak split into three lines.
That’s so amazing.
salicylicacid said
I’m currently analysing 13C spectra and really enjoyed reading your blog entry!
quite helpful and enlightening!
naturalproductman said
I’m glad it helped!
Sina said
This question was asked in my organic exam last week and it’s only know that I found the answer! Thank you