Q3: Arrange each group of compounds from fastest SN2 reaction rate to slowest SN2 reaction rate. CI Cl H3C-Cl CI a) A B C D Br Br b) A B C Br H3C-Br D
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- Arrange these species from fastest SN2 reaction rate to slowest SN2 reaction rate. CH₂CH₂I CH₂CH₂OH CH₂CH₂Cl Fastest Slowest Answer BankQ3: Arrange each group of compounds from fastest SN2 reaction rate to slowest SN2 reaction rate. a) CI Cl فيكم H3C-Cl A B C D Br Br b) A B C Br H3C-Br DRank the following molecules relative reactivity from slowest to fastest under SN1. Br A [Select] [Select] Br B Br [Select] [Select] C Br Hy D H V
- Rank the following molecules in order of increasing relative rate of SN1 reaction with methanol, CH3OH (slowest to fastest reacting). Br Br CH3-Br 1 X X X Br Br 2 5 4 3 C) 5<4<3<2<1 A) 1<2<4<3<5 D) 4 <2<3<5<1 B) 5 < 1<2<4<3 E) 1<2<5<3 <4Based on the structure of the transition state for this reaction, sort the following items based on whether they will increase or decrease the rate of the SN2 reaction. Changes (5 items) (Drag and drop into the appropriate area below) Effect on Rate No more items Increase Use (CH3)30 instead of CH3O¯ change Decrease branch adjacent to I CH3CH2 to CH3 CH3OH as solvent acetone as solventA H2N. Figure 9: Multi-step reaction sequence
- Draw a detailed arrow pushing mechanism for the following reaction. In the rate-determining step unimolecular (SN1) or bimolecular (SN2)Draw a reaction coordinate for the following two SN2 reactions. Label each reaction in the reaction coordinate graph and contrast the two reaction pathways. Clearly label the rate limiting step, any intermediates generated, and the transition state for each step. CI: NaCN, DMSO CI: NaCN, DMSO SN2None