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Advanced Organic Chemistry: Mass spectrum of 1-chloro-2-methylpropane

The mass spectrum of 1-chloro-2-methylpropane

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C4H9Cl (CH3)2CH2Cl mass spectrum of 1-chloro-2-methylpropane fragmentation pattern of m/z m/e ions for analysis and identification of  isobutyl chloride image diagram doc brown's advanced organic chemistry revision notes 

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Interpreting the fragmentation pattern of the mass spectrum of 1-chloro-2-methylpropane

[M]+ is the tiny molecular ion peak (M) with an m/z of 92 corresponding to [C4H9Cl]+, the original 1-chloro-2-methylpropane molecule minus an electron, [(CH3)2CHCH235Cl]+.

Since chlorine has two common isotopes of 35Cl and 37Cl in the ratio 3 : 1, you should observe double peaks in the intensity ratio 3 : 1, two mass units apart for molecular fragments containing a chlorine atom from the fragmentation of 1-chlorobutane.

Two examples of this are quoted in the table below for m/z values of 79 and 77, and 51 and 49, you can see they are roughly in the ratio 3 : 1 in the mass spectrum diagram above.

The very tiny M+1 peak at m/z 93, corresponds to an ionised 1-chloro-2-methylpropane molecule with one 13C atom in it i.e. an ionised 1-chloro-2-methylpropane molecule of formula [13C12C3H935Cl]+

Carbon-13 only accounts for ~1% of all carbon atoms (12C ~99%), but the more carbon atoms in the molecule, the greater the probability of observing this 13C M+1 peak.

1-chloro-2-methylpropane has 4 carbon atoms, so on average, ~1 in 25 molecules will contain a 13C atom.

The most abundant ion of the molecule under mass spectrometry investigation (1-chloro-2-methylpropane) is usually given an arbitrary abundance value of 100, called the base ion peak, and all other abundances ('intensities') are measured against it.

Identifying the species giving the most prominent peaks (apart from M) in the fragmentation pattern of 1-chloro-2-methylpropane.

Unless otherwise indicated, assume the carbon atoms in 1-chloro-2-methylpropane are the 12C isotope.

Some of the possible positive ions, [molecular fragment]+, formed in the mass spectrometry of 1-chloro-2-methylpropane.

m/z value of [fragment]+ 79 77 57 56 51 49
[molecular fragment]+ [CH3CHCH237Cl]+ [CH3CHCH235Cl]+ [(CH3)2CHCH2]+ [C4H8]+ [CH237Cl]+ [CH235Cl]+
m/z value of [fragment]+ 43 42 41 39 29 28 27
[molecular fragment]+ [CH3CHCH3]+ [C3H6]+ [C3H5]+ [C3H3]+ [CH3CH2]+ [C2H4]+ [C2H3]+

Analysing and explaining the principal ions in the fragmentation pattern of the mass spectrum of 1-chloro-2-methylpropane

Atomic masses: H = 1; C = 12; Cl = 35 or 37 (3:1)

Bond enthalpies kJ/mol: C-C = 348;  C-Cl = 338; C-H = 412

Possible equations to explain the most abundant ion peaks of 1-chloro-2-methylpropane

Note the molecular ion peak is very small indicating the molecule fragments very easily.

Formation of m/z 77 and 79 ions:

[(CH3)2CHCH235Cl]+  ===>  [CH3CHCH235Cl]+  or   [CH3CHCH237Cl]+  +  CH3

C-C bond scission to free an end methyl group.

Low probability due to strength of C-C bond, scission of the weaker C-Cl bond more likely.

The ions could also be [CH37ClCH2CH3]+  and  [CH35ClCH2CH3]+.

Mass loss 92 - 15 = 77  and  94 - 15 = 79.

Note the expected 3:1 ratio of intensities expected for chlorine containing fragment ions.

Formation of m/z 57 ion:

[CH3CHClCH2CH3]+  ===>  [CH3CHCH2CH3]+  +  Cl

Formed by the scission of the C-Cl bond, the weakest bond in the 1-chloro-2-methylpropane molecule.

The m/z 57 ion is a secondary carbocation, a stable type of alkyl based ion, the positive charge is stabilised by the +I (inductive) effect of the two alkyl groups.

One reason why the ionised fragments, not containing chlorine, are more likely to be formed, is the more electronegative chlorine tends to make the the chlorine containing fragment retain the electrons.

Formation of m/z 56 ion:

[CH3CHClCH2CH3]+  ===>  [C4H8]+  +  H35Cl  or  H37Cl

Elimination of hydrogen chloride from the parent molecular ion to form an ionised butene fragment.

Mass loss 92 - 36 = 56  and  94 - 38 = 79.

Formation of m/z 43 ion:

[CH3CHClCH2CH3]+  ===>  [C3H7]+  +  CH2Cl

The m/z 43 ion is the base peak ion, the most abundant and 'stable' ion fragment.

C-C bond scission.

Formation of m/z 42 ion:

[?]+  ===>  [C3H6]+  +  ?

Ionised propene molecule formed.

Formation of m/z 41 ion:

[?]+  ===>  [C3H5]+  +  ?

Formation of m/z 39 ion:

[?]+  ===>  [C3H3]+  +  ?

Formation of m/z 29 ion:

[CH3CHClCH2CH3]+  ===>  [CH2CH3]+  +  CH3CHCl

Formation of m/z 27 ion:

[?]+  ===>  [C2H3]+  +  ?

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