Summary

This document provides information on electrophilic addition reactions to alkenes and alkynes, describing different reagents, regioselectivity, stereo selectivity, and intermediates. It includes details on various conditions and products formed.

Full Transcript

7 – Alkenes & Alkynes Alkenes Nomenclature -ene suffix -E/Z Electrophilic Addition Reactions to Alkenes Reagents What’s Regioselectivity Stereo Intermediate Rearrange Added...

7 – Alkenes & Alkynes Alkenes Nomenclature -ene suffix -E/Z Electrophilic Addition Reactions to Alkenes Reagents What’s Regioselectivity Stereo Intermediate Rearrange Added selectivity ments HBr (or HCl, HI) H+ and Br- Markovnikov - carbocation Possible H3O+ H+ and OH- Markovnikov - carbocation Possible + H , ROH H+ and OR- Markovnikov - carbocation Possible Br2/CCl4 Br+ and Br- - Anti bromonium No (or Cl2) ion Br2/H2O Br+ and OH- Markovnikov Anti bromonium No Cl2/H2O Cl+ and OH- ion Br2/ROH Br+ and OR- Markovnikov Anti bromonium No Cl2/ROH Cl+ and OR- ion (1) Hg(OAc)2, H2O H+ and OH- Markovnikov Anti mercurinium No (2) NaBH4 ion (1) Hg(OAc)2, ROH H+ and OR- Markovnikov Anti mercurinium No (2) NaBH4 ion (1) BH3.THF H+ and OH- Anti-Markovnikov Syn - No - (2) H2O2, OH , H2O H2/catalyst H and H - Syn - No (Catalyst = Pd/C, Pt/C, or Ni) HBr/ROOR (peroxide) H. and Br. Anti-Markovnikov - radical No RCO3H (MCPBA) O - Syn - No (1) RCO3H (MCPBA) OH and OH - Anti - No (2) H3O+ (1) OsO4 OH and OH - Syn - No (2) H2O2 KMnO4 (cold, dilute)/ OH- OH and OH - Syn - No Chiral Usual # Centers of products Formed 0 1 1 2 2 Syn = 2 Oxidative Cleavage of Alkenes Anti = 2 Reducing Conditions None = 4 (1) O3, -78C (2) (CH3)2S or Zn/H2O Oxidizing Conditions (1) O3 (2) H2O2 KMnO4 (hot, concentrated)/OH- (or with H3O+) ChadsPrep.com 19

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