- 1 2 B Na Oet H C C C Li A Proton Transfer Lewis Acid Base D Electrophilic Addition E E1 Elimination C Radic 1 (218.7 KiB) Viewed 12 times
1. 2. b Na OEt H₂C-C=C: Li a = Proton transfer = Lewis acid/base d = Electrophilic addition e = E1 Elimination C = Radical chain f = E2 substitution Elimination g = SN1 Nucleophilic substitution h = SN2 Nucleophilic substitution OEt + NaBr Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. LiBr
1. 2. a = Proton transfer b = Lewis acid/base Br₂ Cl₂ 180° hv d = Electrophilic addition e = E1 Elimination c = Radical chain f = E2 substitution Elimination ta Br Br e g = SN1 Nucleophilic substitution + h = SN2 Nucleophilic substitution HCI Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. HBr
Draw a structural formula for the substitution product of the reaction shown below. ▼ H3C • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Center If more than one stereoisomer of product is formed, draw both. do-8 Separate multiple products using the + sign from the drop-down menu. MAVIL Br / CH3OH ? ChemDoodle n[F Previous Next
Draw a structural formula for the substitution product of the reaction shown below. ● CI X111. MAVIL CH3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one stereoisomer of product is formed, draw both. H₂O Separate multiple products using the + sign from the drop-down menu. ? O. Sn [F Previous Next