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2-Bromo-3-methylbutane, rearrangement in hydrolysis

Why does the carbocation intermediate in the hydrolysis of 2 bromo 3 methylbutane rearrange by way of a hydride shift rather than a methyl shift ... [Pg.345]

Additional evidence for carbocation intermediates in certain nucleophilic substitutions comes from observing rearrangements of the kind normally associated with such species For example hydrolysis of the secondary alkyl bromide 2 bromo 3 methylbutane yields the rearranged tertiary alcohol 2 methyl 2 butanol as the only substitution product... [Pg.344]

Carbocation Rearrangement in the SnI Hydrolysis of 2-Bromo-3-methylbutane THE OVERALL REACTION ... [Pg.340]

See other pages where 2-Bromo-3-methylbutane, rearrangement in hydrolysis is mentioned: [Pg.1218]    [Pg.1218]    [Pg.322]   
See also in sourсe #XX -- [ Pg.339 ]



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2 Bromo 2 methylbutane

2 Bromo 3 methylbutane rearrangement

2 Bromo 3 methylbutane rearrangement hydrolysis

2 Methylbutane

2- Methylbutan

2-Bromo-2-methylbutane hydrolysis

3- methylbutanal

Hydrolysis rearrangement

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