6. How many intermediates are present/formed from the diatomic halogenation (Br₂) of 2-butene? A. 0 B. 1 C. 2 D. 3 E. 4

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6 How Many Intermediates Are Present Formed From The Diatomic Halogenation Br Of 2 Butene A 0 B 1 C 2 D 3 E 4 1 (359.94 KiB) Viewed 11 times

6. How many intermediates are present/formed from the diatomic halogenation (Br₂) of 2-butene? A. 0 B. 1 C. 2 D. 3 E. 4 7. Which of the following compounds will generate the most stable carbocation upon initial protonation with an acid (H+)? A. B. C. D. E. 8. Which of the following is true. A. Diatomic halogenation undergoes a "syn" reaction mechanism. B. Hydrohalogenation and hydration undergo carbocation-based mechanism. Hydrogenation reactions undergo a "syn" reaction mechanism. D. Both (B) and (C) are correct. E. (A), (B), and (C) are incorrect. 9. What is the expected major product of the following acid-catalyzed hydration reaction? (No stereochemistry has been shown purposely for this problem) Me B. HCI H₂O OH C. HO. D. OH OH E. None are correct