(A) the most stable? (B) (c) (D) (E) 2. Which alkene is a Z-isomer? (A) (B) (c) (D) (E) 3. Which of the following would be obtained from Hofmann elimination of 2-chloro-2-methylpentane?? (A) (B) (C) (D) (E) 4. Which of the following would be obtained from Zaitsev elimination of 2-bromo-2-methylpentane? (A) (B) (C) (D) (E) 5. If allowed to react with Cl2, which alkene would give a product with chiral centers but optically inactive (A) (B) (C) (D) (E) 6. Which alcohol below would undergo acid-catalyzed dehydration with the slowest rate at a given te concentration of acid? OH OH (A) (B) OH (C) (D) 7. What would be the major elimination product obtained from the reaction below? EtONa Br X EtOH (A) OH (B) (c) (D) No reaction is exp
(A) the most stable? (B) (c) (D) (E) 2. Which alkene is a Z-isomer? (A) (B) (c) (D) (E) 3. Which of the following would be obtained from Hofmann elimination of 2-chloro-2-methylpentane?? (A) (B) (C) (D) (E) 4. Which of the following would be obtained from Zaitsev elimination of 2-bromo-2-methylpentane? (A) (B) (C) (D) (E) 5. If allowed to react with Cl2, which alkene would give a product with chiral centers but optically inactive (A) (B) (C) (D) (E) 6. Which alcohol below would undergo acid-catalyzed dehydration with the slowest rate at a given te concentration of acid? OH OH (A) (B) OH (C) (D) 7. What would be the major elimination product obtained from the reaction below? EtONa Br X EtOH (A) OH (B) (c) (D) No reaction is exp
Chapter5: Stereochemistry At Tetrahedral Centers
Section5.SE: Something Extra
Problem 70AP
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