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Allylic carbocation, electrostatic stability

Allylic bromination, 339-340 mechanism of, 339-340 Allylic carbocation, electrostatic potential map of, 377, 489 resonance in, 488-489 SN1 reaction and, 376-377 stability of, 488-489 Allylic halide, S l reaction and. 377 S j2 reaction and, 377-378 Allylic protons, ]H NMR spectroscopy and, 457-458... [Pg.1285]

The electrostatic potential maps in Figure 16.2 compare the resonance-stabilized allyl carbocation with CH3CH2CH2, a localized 1° carbocation. The electron-deficient region—the site of the positive charge—is concentrated on a single carbon atom in the 1° carbocation CH3CH2CH2 . In the allyl carbocation, however, the electron-poor region is spread out on both terminal carbons. [Pg.573]

See other pages where Allylic carbocation, electrostatic stability is mentioned: [Pg.82]    [Pg.273]   
See also in sourсe #XX -- [ Pg.488 ]

See also in sourсe #XX -- [ Pg.488 ]

See also in sourсe #XX -- [ Pg.506 ]



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Allylic carbocation, electrostatic

Allylic carbocations

Allylic stabilization

Allyls stabilization

Carbocation stability

Carbocation stabilization

Carbocations allyl

Carbocations stability

Carbocations stabilization

Carbocations stabilized

Electrostatics stabilization

Stability electrostatic

Stabilization electrostatic

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