Naturalproductman’s Blog

Hey, is that a natural product?!

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.

About these ads

3 Responses to “Why is CDCl3 a Triplet?”

  1. I’m currently analysing 13C spectra and really enjoyed reading your blog entry! :) quite helpful and enlightening!

  2. Sina said

    This question was asked in my organic exam last week and it’s only know that I found the answer! Thank you :)

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Connecting to %s

 
Follow

Get every new post delivered to your Inbox.

Join 49 other followers

%d bloggers like this: