I was looking at this example in my textbook and saw that there is a small peak at the end for an m/z of 59 and 60 for both propanal and propanone? How did this arise if the relative molecular mass of both molecules are 58?
I was looking at this example in my textbook and saw that there is a small peak at the end for an m/z of 59 and 60 for both propanal and propanone? How did this arise if the relative molecular mass of both molecules are 58?
The presence of hydrogen isotopes and other isotopes.
I was looking at this example in my textbook and saw that there is a small peak at the end for an m/z of 59 and 60 for both propanal and propanone? How did this arise if the relative molecular mass of both molecules are 58?
Probably due to carbon 13 and other O isotopes rather than H isotopes.
On consideration, I see that you are quite right. Carbon 13 makes up over 1% of naturally occurring carbon, while deuterium is only about 0.02%.
My first thought was that as there are many hydrogen atoms in the structures the deuterium would also be significant, but even with butane this only has a minor contribution compared to 13C.
On consideration, I see that you are quite right. Carbon 13 makes up over 1% of naturally occurring carbon, while deuterium is only about 0.02%.
My first thought was that as there are many hydrogen atoms in the structures the deuterium would also be significant, but even with butane this only has a minor contribution compared to 13C.