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- 4Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OHComplete the reactions below, draw the mechanism for each reaction, and determine majorand minor products where applicable.
- Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?can you show the mechanism?Draw the curved arrows for the following mechanisms. Describe what is hap step (mechanism patterns). (Take it one step at a time and note the differences). :0: R CI: H-O-H :Ö:0 :0: :CI: :CI: H2O OH OH2 Br Br H-Br O-H H-8-H :0: OH Br 1 Br H2O H₂O
- Draw 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.Which of the following is an intermediate in the reaction sequence shown in the box? КОН, Н,ОEТОН | ? 1. (CH3)2CULI gentle heat 2. HС, Н,О A) B) ОН D) O A В C O: O: O=(4d) and PhMgBr, followed by reaction with the acid. Please draw that mechanism here! Even though benzoic acid is reformed as the product, a reaction does take place between benzoic acid 1. PhMgBr HO, 2. H30*