Question: Example: A. SN2 reaction: I + H3CHCl C-Br B. SN1 reaction H R 100% H3C R 100% C-Br S 50% H CCHCH3 CH3 S 100%

Example: A. SN2 reaction: I + H3CHCl C-Br B. SN1 reaction H R 100% H3C R 100% C-Br S 50% H CCHCH3 CH3 S 100% P27. What is (are) the major difference(s) between the reactions (A) and (B)? Br CII R 50% + Br P28. What must happen mechanistically before the nucleophile can attack if we are to see the R product? P29. This transformation goes through a planar reactive intermediate. As such, what is formed on the electrophilic carbon if it becomes a planar reactive intermediate

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