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Kinetics of Isomerizations Involving Arenium Ions

After characterizing the rates of the 1,2-shift of hydrogen and different groups it is reasonable to return to isomerizations of substituted benzenium ions. Isomerization of methylated benzenes In HF—SbFj at 25 °C o- and p-xylenes are present as ions (105) and (106) which are further practically completely converted to a conjugate acid of m-xylene, i.e. ion (JOT). [Pg.164]

By conventional kinetic methods, the rate coefficients for the transformation of ions (105) and (106) into ion (107) is determined. Similarly, one can find the rate [Pg.164]

The rate coefficients for most of the mentioned transformations are listed in Table 53 [Pg.165]

The data obtained from the degenerate rearrangements of benzenium ions testify that the rate coefficients of intraionic 1,2-hydrogen shifts are usually by several [Pg.165]

Reaction 10 k (s- ) AG kcal/mole Stage of 1,2-CH3-shift 10 kcHj (s- ) AOc h, kcal/mole GcHj kcal/mole [Pg.165]


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