Please draw it out, thank you с 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 or Cl or Br or or 10 Ха Br
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- 2) Rank the following compounds in order of their reaction rates in an SN1 reaction with NaF with 1 being the fastest reaction and 5 being the slowest. OTs Br CIExamine the following reactions, then label each with the mechanism that is mostlikely to occur: ( circle correct choices)attack under the given reaction conditions? carbon is most likely to undergo a nucleophilic (A) II is more likely to be attacked because it has a larger partial positive charge. (B) I is more likely to be attacked because it has a larger partial positive charge. ***** (C) II is more likely to be attacked because it has less steric hindrance. (A) (D) I is more likely to be attacked because it has less steric hindrance. 47. Which alkene will generate the product of this reaction sequence? (C) ? 1. 1) CH₂CH₂MgBr 2) H O R O H 2.00 CN OH (B) (D) K 48. Which are possible enol tautomers of 7-methyl-3-pentanone? HO Et 겨 Et racemic OH H CN OH
- PO-13. Rank from slowest to fastest rate of SN1 substitution. Br Br Br II III (A) Iqu7 I cannot understand why the directions have been changed Why does a is a Sn2 even thought it is a tertiary carbons?Which nucleophilic substitution reaction (s) should occur readily? A) B) C) D) E) I only Il only III only Both II and III I, II, & III I II III 0 NH₂ i + CH3OH + CH3OH i G + CH3OH OCH 3 OCH 3 OCH 3 + NH3 + HCI + HOẠc 16Which is the major substitution product of the reaction shown? (A) OEt (C) (E) no reaction Br NaOEt © 2019 ProtonGuru.com (B) (D) OEt (F) a mixture of more than one9.17 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 BrGive detailed Solution with explanation needed..give correct answerIdentify the best conditions to complete the SN2 reaction shown below. A) CH3I, THF B) CH3CH₂I, THE C) CH3CH₂CCNa, THF D) CH3CH₂CCNA, CH3OH E) KI, THFdon 13. (1) Draw the (E)- and (Z)- isomers of 1,3-dichloro-2-methylbut-2-ene. Using curved arrows, draw (a) an SN2 mechanism and (b) and SN1 mechanism for the substitution reaction shown below. Br ) Draw the organic product(s) formed in the following reactions: 1)0, by 2) Zn. H,0 MShow a sequence of reactions that could be used to synthesize the following compound. You must start from 3-pentanol. No mechanisms needed (HINT: You wil need to bring together more than one of the reactions you have seen in Modules 3 and 4]Give correct answer to all parts?SEE MORE QUESTIONS