Nitration of pseudocumene (1,2,4-trimethyl-benzene) produces 5- and 6-nitropseudocumenes in the ratio 9:1 under conditions where there is evidence that both C-5 and C-6 are activated sufficiently to react upon encounter, showing the necessity for including in the kinetic scheme an intermediate preceding Wheland intermediate formation.
R. B. Moodie, K. Schofield and J. B. Weston, J. Chem. Soc., Chem. Commun., 1974, 382 DOI: 10.1039/C39740000382
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