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SUMMARY OF REACTIONS BY TYPE, CHAPTERS

Sn2 Chapter 6 See Section 6.14 for a summary of nucleophiles mentioned in early chapters inversion 1°, 2°,benzylic(l°or2°), or allylic (1° or 2°) leaving group (e.g., halide, tosylate, mesylate) strong nucleophile polar aprotic solvent [Pg.301]

Radical substitution racemization (via radical) 3°, benzylic, or allylic hydrogen  [Pg.301]

Type Stereochemical/Regiochemical Result Favoring Conditions [Pg.301]

E2 (dehydrohalogenation) elimination to form the most strong base [Pg.301]

Section 7.6 elimination) with small bases KOH/EtOH, tert-BuOK/rerr-BuOH)  [Pg.301]

See other pages where SUMMARY OF REACTIONS BY TYPE, CHAPTERS is mentioned: [Pg.301]   


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