The mass spectra of twenty‐eight monosubstituted trans‐stilbenes in ortho, meta, para and alpha positions with N(CH3)2, NH2, OCH3, OH, Br, Cl, F, CH3, COOH, CN and NO2 groups as substituents have been studied. A detailed fragmentation pathway is given for stilbene. This fragmentation, characteristic for most of the substituted stilbenes, takes place either from the molecular or from the [M ‐ Substituent] ion. In o‐nitro‐, o‐methoxy‐,α‐carboxyl‐ and α‐methylstilbene, however, rearrangement reactions prior to fragmentation influence the fragmentation pattern.
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Güsten et al. (1974) studied this question.
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