Q3: 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 D
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reaction rate.
a)
CI
Cl
فيكم
H3C-Cl
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B
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- Arrange these species from fastest SN2 reaction rate to slowest SN2 reaction rate. CH₂CH₂I CH₂CH₂OH CH₂CH₂Cl Fastest Slowest Answer BankRank the following substrates in order from slowest SN2 reaction rate to fastest. Br Br Br H3C Br A B DBased 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 solvent
- Rank 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 VDraw a reasonable reaction mechanism.The cis isomer of 1-bromo-4-tert-butylcyclohexane undergoes E2 elimination about 1,000 times faster than the trans isomer. Explain why the cis isomer reacts faster. Hint: It is not because of steric hindrance. Br + NaOH Fast (H3C),C (H3C);C Br + NaOH Slow (H3C);C' (H3C);C
- From the following reaction are step 1 and 2 correct?, explain why or why not and draw the whole mechanismIdentify the best conditions to complete the SN2 reaction shown below. A) CH3I, THF B) CH3CH₂I, THE C) CH3CH₂CCNa, THF D) CH3CH₂CCNA, CH3OH E) KI, THFWhich of the following compounds will undergo the fastest SN1 reaction? A B IV || C) III E Both I & IV || Br E IV Br
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