flashcards - Definition Face of Card: Flash Card, Type II:...

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R-Cl R--OH + PCl 3 1 o , 2 o , 3 o R-Cl 3 o R-OH + conc. HCl R-Cl ZnCl 2 R-OH + conc. HCl 2 o 1 o ZnCl 2 R-Cl R-OH + conc. HCl 1 o , 2 o , 3 o R-Cl + SO 2 + HCl R--OH + SOCl 2 Back of Card: R-Cl R-OH Flash Card, Type I: Reagent(s) for functional group transformation Face of Card: Flash Card, Type III: Sources of functional groups Face of Card: Back of Card: R-H + Br 2 R-OH + conc. HBr light or heat Free radical chain; selectivity Polar reaction mechanism R-OH + PBr 3 heat No mechanism given R 2 C=CR 2 + conc. HBr Electrophilic addn mech Back of Card: Flash Card, Type IV:
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Unformatted text preview: Definition Face of Card: Flash Card, Type II: Reaction Mechanism Face of Card: Electrophilic Addition to Alkene Back of Card: Constitutional Isomers Molecules having identical molecular formulae but different atomic connectivities, i.e., bonding patterns R-Br E Nu Nu-E Nu +-E E-Nu: :B E + E E-Nu: Examples of "E-Nu:" are HCl (aq) (= H 3 O + Cl-), Cl 2 . In case of Br 2 , cyclic bromonium ion , rather that open carbocation is formed....
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This note was uploaded on 09/26/2008 for the course CH 318N taught by Professor Willson during the Spring '08 term at University of Texas at Austin.

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