Conclusions
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1.
Breakdown of derivatives of 2,6-di-tert-butyl-p-benzoquinone under electron impact proceeds, in part, through tert-butyl group splitting and, in part, through specific reactions of position 4 substituents.
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2.
2,6-Di-tert-butyl-p-nitrosophenol exists as a quinoid form in the gaseous phase, while the phenylhydrazone of 2,6-di-tert-butyl-p-benzoquinone exists as a tautomer of 3,5-di-tert-butyl-4-hydroxyazo-benzene.
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Translated from. Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 825–828, April, 1978.
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Krokhin, A.V., Chizhov, O.S., Ershov, V.V. et al. Mass spectra of certain derivatives OF 2, 6-di-tert-butyl-p-benzoquinone. Russ Chem Bull 27, 711–714 (1978). https://doi.org/10.1007/BF00925290
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DOI: https://doi.org/10.1007/BF00925290