• Each?peak?in the mass spectrum corresponds to a certain?fragment?with a particular?m/e?value
• The peak with the highest?m/e?value is the molecular ion (M⁺) peak which gives information about the?molecular?mass?of the compound
• The molecular ion is the entire molecule that has lost one electron when bombarded with a beam of electrons

• The?[M+1]?peak is a smaller peak which is due to the natural abundance of the isotope carbon-13
• The height of the [M+1] peak for a particular ion depends on how many carbon atoms are present in that molecule; the more carbon atoms, the larger the [M+1] peak is
  • For example, the height of the [M+1] peak for an hexane (containing six carbon atoms) ion will be greater than the height of the [M+1] peak of an ethane (containing two carbon atoms) ion

Worked example: Analysing mass spectra

Answer

The mass spectrum corresponds to propanal as the molecular ion peak is at?m/e?= 58

Propanal arises from the CH₃CH₂CHO⁺?ion which has a molecular mass of 58

Butanal arises from the CH₃CH₂CH₂CHO⁺?ion which has a molecular mass of 72

• The molecular ion peak can be used to identify the?molecular mass?of a compound
• However, different compounds may have the same molecular mass
• To further determine the structure of the unknown compound,?fragmentation?is used
• Fragments may appear due to the formation of?characteristic?fragments?or the?loss?of?small?molecules
  • For example, a peak at 29 is due to the characteristic fragment C₂H₅⁺--
  • Loss of small molecules give rise to peaks at 18 (H₂O), 28 (CO), and 44 (CO₂)

Alkanes

• Simple alkanes are fragmented in mass spectroscopy by breaking the C-C bonds
• M/e?values of some of the common alkane fragments are given in the table below

m/e?values of fragments table

Mass spectrum showing fragmentation of alkanes

Halogenoalkanes

• Halogenoalkanes often have multiple peaks around the molecular ion peak
• This is caused by the fact that there are different isotopes of the halogens

Mass spectrum showing different isotopes of the halogens in the molecular ion

Alcohols

• Alcohols often tend to lose a?water molecule?giving rise to a peak at?18 below the molecular ion
• Another common peak is found at?m/e?value 31 which corresponds to the CH₂OH^+-- fragment
• For example, the mass spectrum of propan-1-ol shows that the compound has fragmented in four different ways:
  • Loss of H??to form a C₃H₇O⁺?fragment with?m/e?= 59
  • Loss of a water molecule to form a C3H6+?fragment with?m/e?= 42
  • Loss of a??C₂H₅?to form a CH₂OH⁺?fragment with?m/e?= 31
  • And the loss of??CH2OH to form a C₂H₅⁺?fragment with?m/e?= 29

Mass spectrum showing the fragmentation patterns in propan-1-ol (alcohol)

Worked example: Ion fragmentation

Answer

The correct answer is?4?as bromomethane (CH3Br) will fragment into 3 peaks

• • CH₃⁸¹Br → [CH₃⁸¹Br]⁺?+ e^??at m/e 96
  • CH₃⁷⁹Br → [CH₃⁷⁹Br]⁺?+ e^??at m/e 94
  • CH₃Br → [CH3]⁺?+??Br at m/e 15

The last two peaks (which correspond to the molecular ion peak) therefore are equal in size and occur at?m/e?values of 94 and 96

Worked example: Alcohol fragmentation

Answer

The correct answer is?4?because a line at m/e = 43 corresponds to an ion with a mass of 43 for example:

• • [CH₃CH₂CH₂]⁺
  • [(CH₃)₂CH]⁺

2-butanol is not likely to have a fragment at m/e = 43 as it does not have either of these fragments in its structure.