Table 1.
Possible oxidative structures of tested monoterpenes related to observed molecular ions.
Molecular ion | Formula | Change in MW | Oxidative product | Explanation |
---|---|---|---|---|
132 | C10H12 | M-4 | − 4[H] | Loss of 4 hydrogens to form two double bonds from two –CH2–CH2− group |
134 | C10H14 | M-2 | − 2[H] | Loss of 2 hydrogens to form an double bond from –CH2–CH2− |
136 | C10H16 | M | Parent compound or its isomers | |
138 | C9H14O | M + 2 | + [O] and −[CH2] | Replacing –CH2- group with an oxygen |
150 | C10H14O | M + 14 | + [O] and − 2[H] | Formation of C=O group from –CH2− |
152 | C10H16O | M + 16 | + [O] | Insertion of oxygen between C and H in –CH2− CH2− group to form hydroxyl group, or addition of oxygen to a double bond to form epoxide group |
154 | C10H18O | M + 18 | + [O] and + 2[H] | Addition of OH and H to a double bond |