If you like us, please share us on social media, tell your friends, tell your professor or consider building or adopting a Wikitext for your course.
This page explains how to find the relative formula mass (relative molecular mass) of an organic compound from its mass spectrum. It also shows how high resolution mass spectra can be used to find the molecular formula for a compound.
When the vaporised organic sample passes into the ionisation chamber of a mass spectrometer, it is bombarded by a stream of electrons. These electrons have a high enough energy to knock an electron off an organic molecule to form a positive ion. This ion is called the molecular ion.
The molecular ion is often given the symbol M+ or - the dot in this second version represents the fact that somewhere in the ion there will be a single unpaired electron. That's one half of what was originally a pair of electrons - the other half is the electron which was removed in the ionisation process.
The molecular ions tend to be unstable and some of them break into smaller fragments. These fragments produce the familiar stick diagram. Fragmentation is irrelevant to what we are talking about on this page - all we're interested in is the molecular ion.
In the mass spectrum, the heaviest ion (the one with the greatest m/z value) is likely to be the molecular ion. A few compounds have mass spectra which don't contain a molecular ion peak, because all the molecular ions break into fragments. That isn't a problem you are likely to meet at A'level.
For example, in the mass spectrum of pentane, the heaviest ion has an m/z value of 72.
Because the largest m/z value is 72, that represents the largest ion going through the mass spectrometer - and you can reasonably assume that this is the molecular ion. The relative formula mass of the compound is therefore 72.
Finding the relative formula mass (relative molecular mass) from a mass spectrum is therefore trivial. Look for the peak with the highest value for m/z, and that value is the relative formula mass of the compound. There are, however, complications which arise because of the possibility of different isotopes (either of carbon or of chlorine or bromine) in the molecular ion. These cases are dealt with on separate pages.
So far we've been looking at m/z values in a mass spectrum as whole numbers, but it's possible to get far more accurate results using a high resolution mass spectrometer. You can use that more accurate information about the mass of the molecular ion to work out the molecular formula of the compound.
For normal calculation purposes, you tend to use rounded-off relative isotopic masses. For example, you are familiar with the numbers:
To 4 decimal places, however, these are the relative isotopic masses:
The carbon value is 12.0000, of course, because all the other masses are measured on the carbon-12 scale which is based on the carbon-12 isotope having a mass of exactly 12.
Two simple organic compounds have a relative formula mass of 44 - propane, C3H8, and ethanal, CH3CHO. Using a high resolution mass spectrometer, you could easily decide which of these you had. On a high resolution mass spectrometer, the molecular ion peaks for the two compounds give the following m/z values:
You can easily check that by adding up numbers from the table of accurate relative isotopic masses above.
A gas was known to contain only elements from the following list:
The gas had a molecular ion peak at m/z = 28.0312 in a high resolution mass spectrometer. What was the gas?
After a bit of playing around, you might reasonably come up with 3 gases which had relative formula masses of approximately 28 and which contained the elements from the list. They are N2, CO and C2H4. Working out their accurate relative formula masses gives:
The gas is obviously C2H4.
An NSF funded Project