1. 2. Ph 1. Ph 2 OH AlBrs a = Proton transfer b = Lewis acid/base c = Radical chain substitution NMe₂ H₂SO4 Ph Ph NMe₂ Tamoxifen anti (brest) cancer drug AlBr J Ph Ph C d = Radical chain addition e = Electrophilic addition f = E1 Elimination NMе₂ Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution iSN2 Nucleophilic substitution

1. 2. 1. -CH3 H Ph HO 2. + E2 Elimination aqueous H₂SO4 a = Electrophilic addition b = C = SN1 Nucleophilic substitution f = Carbonyl nucleophilic addn Submit Answer NaOH Retry Entire Group OH CH3 d Ph = SN2 Nucleophilic substitution g e Electrophilic aromatic substitution h = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. = 6 more group attempts remaining Nucleophilic subs at carbonyl(acyl Xfer) Conjugate (nucleophilic) addn

10:08 AM Thu Mar 23 ← Problem 35 of 23 Draw the major product of this reaction. Ignore inorganic byproducts. + AICI 3 > @ 66% O Submit

1. 2. Å 1. N-Br a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. H₂SO4 DMSO / H₂O OH love Br ..OH d = Radical chain addition e= Electrophilic addition f = E1 Elimination + Een N-H Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

1. 2. H₂C 1. MeO 2. -CH3 H₂O a = Proton transfer b = Lewis acid/base c = Radical chain substitution H3PO4 80° MeO CH3 H₂COM₂ CH3 d = Radical chain addition e = Electrophilic addition f = E1 Elimination H₂O Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g = E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

1. 2. Br 1. + H₂O a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. NaOH Aqueous acetone OH + OH 앳 H OH + + HBr d = Radical chain addition e = Electrophilic addition f = E1 Elimination Nal Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

2. OH 1. Mg2+ Br 2. a = Proton transfer b= Lewis acid/base c = Radical chain substitution H₂SO4 140⁰ H₂SO4/ H₂O Submit Answer [Review Topics] H₂O + H₂O + Mg2+ Br d = Radical chain addition e= Electrophilic addition f E1 Elimination [References] Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Retry Entire Group 9 more group attempts remaining HSO g=E2 Elimination h = SN1 Nucleophilic substitution i= SN2 Nucleophilic substitution Previous Next Sho

1. 2. Ph 1. Ph OH a Proton transfer b = Lewis acid/base c = Electrophilic addition 2. + Na CN NMe₂ DMF H₂SO4 Ph Ph H3C H CH3 H CN OH NM²₂ Tamoxifen anti (brest) cancer drug Ph d E1 Elimination = e = E2 Elimination Ph NMe₂ The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a- g for your answers. f = SN1 Nucleophilic substitution gSN2 Nucleophilic substitution

1. 2. HO a = Proton transfer b = Lewis acid/base 1. f 2. toto. H₂SO4 Submit Answer -CH3 Aqueous acetone e = Electrophilic addition f = E1 Elimination g=E2 Elimination OH H₂O Retry Entire Group 1 more group attempt remaining K ...OH = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. + HO-S -CH3 h SN1 Nucleophilic substitution i SN2 Nucleophilic substitution j = Electrophilic aromatic substitution

1. 2. ~ 1 OH 2. Ph NaBr Submit Answer 8 a = Proton transfer b = Lewis acid/base c = Radical chain substitution d = Radical chain addition 00 100⁰ Ph H₂SO4 Retry Entire Group H₂ th polystyrene Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a answers. e = Electrophilic addition f = E1 Elimination g = E2 Elimination H₂O 8 more group attempts remaining h SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution j = Electrophilic aromatic substitution Previ Email Instr