b. Discuss the mechanism for any two of the reactions shown in Figure 4. Include all curly arrows, as well as any relevant stereochemistry considerations in your answer. (i) (ii) (iii) H Ph Br OH NaCN HO HCI MeOH NEt3 C4H7NO + NaCl A H₂SO4 catalyst C8H8O2 + Br B ✪ HNEt3 C7H1402 + H₂O C
b. Discuss the mechanism for any two of the reactions shown in Figure 4. Include all curly arrows, as well as any relevant stereochemistry considerations in your answer. (i) (ii) (iii) H Ph Br OH NaCN HO HCI MeOH NEt3 C4H7NO + NaCl A H₂SO4 catalyst C8H8O2 + Br B ✪ HNEt3 C7H1402 + H₂O C
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 54AP
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CH2023 Q2 (b)
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VIEWStep 2: A) Propanal reacting with NaCN in HCl to give propylcyanihydrine
VIEWStep 3: B) Phenylbromide reacting with methanol using triethylamine to give ester formation (methyl phenyl e
VIEWStep 4: C) Ethanoic acid reacting with 4-methylpentanol to give ester formation:
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