9.17 Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone. (a) ▸ Details (b) ▸ Details (c) (d) ▸ Details Br محمد or or Br ог ог Ха Br
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- 9.64 Draw the products of each reaction, and indicate the stereochemistry where appropriate. CH;CO, f. OH TSCI pyridine (1] N2OCH, h. (2] H,0Draw the mechanism for each of the following reactions shown below. Show all steps in the reaction with the intermediates formed at each step, and use curved arrows to track the glow of electron.G.60.
- (80) What is the major organic product for the following reaction?(55) For the following is a 3-step synthesis problem, you are given: the Starting Material and the Product; a scheme of the expected conditions/intermediates and a list of 21 possible conditions and intermediates. Put the correct conditions/intermediates in the correct order to achieve this transformation.Which nucleophile in each pair is more reactive?
- In the following Sn1/E1 reaction three elimination products are formed. Which El product do you think would have the highest yield? 1. B C CI CH,CH,OH major E1 product heat 1) 2) 3) 2. 3. A8.77 Substitution vs. Elimination: Identify the major and minor productis) for each of the following reactions: ? 1-BUOK (a) OTs NAOH он conc. H,SO, ? NaCi Нeat (d) OTs DMSO (c)8.18a Modify the given carbon skeleton to draw the major product of the given reaction. Use the single bond tool to interconvert between double and single bonds. 1) Вн, THF 2) HO, NaOH H,C CH2 * Edit Drawing Save for Later Attempts: 0 of 15 used Submit Answer 3:04 PM P Type here to search 15°F A G 40 ENG 2/5/2022
- (63) For the following is a 3-step synthesis problem, you are given: the Starting Material and the Product; a scheme of the expected conditions/intermediates and a list of 21 possible conditions and intermediates. Put the correct conditions/intermediates in the correct order to achieve this transformation.79 3. Complete the following reaction and write a mechanism for both the substitution and elimination products (both substitution and elimination products occur simultaneously). Discuss all criteria including stereochemistry when a chiral secondary primary alkyl halide with (S) configuration reacts with methanol a weak nucleophile. Draw energy profile for this reaction. (4 points) CH2CH3 CH₂O-Na+ + Br H3C (S) no 1999b 02.907 90 +20110Please Write SteP by Step Answer Otherwise I give you DISLIKES !