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The presence of a prominent peak at <jats:italic>m\/z<\/jats:italic> 121 for an elimination of a dihydrogen molecule renders the ortho\u2010isomer spectrum markedly different from those of its meta and para congeners. Investigations carried out with deuterium\u2010labeled isotopologues of the ortho isomer verified that the labile hydrogen atom on the hydroxyl group and one of the benzylic hydrogen atoms are specifically removed in the formation of the <jats:italic>m\/z<\/jats:italic> 121 ion. The ortho\u2010isomer spectrum also showed a prominent peak at <jats:italic>m\/z<\/jats:italic> 93. Experimental data indicated that the <jats:italic>m\/z<\/jats:italic> 93 product ion originates either from a two\u2010step H<jats:sub>2<\/jats:sub>and CO elimination mechanism or from a direct loss of a HCHO molecule from the precursor anion. The intensity ratio of the <jats:italic>m\/z<\/jats:italic> 93 and 94 peaks in the spectrum recorded from the <jats:italic>m\/z<\/jats:italic> 124 ion generated from a sample of <jats:italic>o<\/jats:italic>\u2010hydroxybenzyl alcohol dissolved in D<jats:sub>2<\/jats:sub>O supported the notion that the direct HCHO loss is the more dominant pathway for the generation of the phenolate ion under low activation conditions. In contrast, the two\u2010step mechanism becomes the more dominant pathway under high collisional activation conditions. The spectrum also showed a weak peak at <jats:italic>m\/z<\/jats:italic> 105 for a water loss. Based on computational data, the <jats:italic>m\/z<\/jats:italic> 105 ion generated in this way appears to be a composite generated from a common ion\u2010neutral complex intermediate in which a hydroxyl anion is positioned equidistantly between one of the benzylic hydrogens and a nearby hydrogen atom of the benzene ring. Upon activation, the complex dissociates to form either a phenide or a quinone methide anion. The reaction forming a carbon dioxide adduct under ion\u2010mobility conditions was used to support the proposed water\u2010loss mechanism.<\/jats:p>","DOI":"10.1002\/jms.4829","type":"journal-article","created":{"date-parts":[[2022,4,9]],"date-time":"2022-04-09T07:08:14Z","timestamp":1649488094000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Fragmentation pathways of deprotonated <i>ortho<\/i>\u2010hydroxybenzyl alcohol"],"prefix":"10.1002","volume":"57","author":[{"given":"Meenu","family":"Kumar","sequence":"first","affiliation":[{"name":"Center for Mass Spectrometry, Department of Chemistry, Chemical Biology and Biomedical Engineering Stevens Institute of Technology  Hoboken New Jersey USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhaoyu","family":"Zheng","sequence":"additional","affiliation":[{"name":"Center for Mass Spectrometry, Department of Chemistry, Chemical Biology and 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