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- Devise a 4-step synthesis of the product from the starting material. CH3 1. reagent 1 2. reagent 2 H3C HO. 3. reagent 3 4. reagent 4 H3C H. Select reagent 1: Select reagent 2: NH, CH,, cat. H,0+ CH, MGB. Select reagent 4: H, Pd NaBH, LIAIH,5. Predict the major product for each of the following reactions. Include stereochemistry when appropriate. Draw the mechanism for each reaction. a. b. C. d. e. Br CI OH CI H₂O NH3 OTS NaCN MeCN KOPh acetone5. Predict the major product for each of the following reactions. Include stereochemistry when appropriate. Draw the mechanism for each reaction. a. b. C. d. e. CI Br OH Lor CI LOTS OTS H₂O NH3 NaCN MeCN KOPh acetone
- 5. Predict the major product for each of the following reactions. Include stereochemistry when appropriate. Draw the mechanism for each reaction. a. b. C. d. OH H₂O NH3 NaCN MeCN KOPh acetoneIdentify the reagents needed to come up with the given compounds. Pls Separate the reagents with a comma and a space. (ex. HNO3, H2SO4). For a multi-step reaction, separate the reagents with a semi-colon. (ex. HNO3, H2SO4; CH3Cl, AlCl3) There should be 9 reagentsMatch each reaction with its type. H,0* + CH,NH, но Choose.. Choose... E2 H,O* Nucleophilic Acyl Substitution OH но H,0 Nucleophilic Addition SN2 Electrophilic Addition HCI E1 heat None of the above SN1
- 3. Provide the product(s) or reagent(s) as appropriate. CI ? 1. H₂O, H₂SO4 2. H₂CRO4 1. NaOH 2. H₂CRO4 ? ? ? H1. Give the major product(s) of the following reactions as needed. Include any stereoisomers. NaOEt 1. Br NaOH Br 2. NaOtBu 3. A MEOH 4. Br 2. Which reaction will proceed faster A or B? H,S H2S "CI .... вDetermine 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 + CH3CH₂OH
- reactions. Draw mechanis.mandspecify What are the products fallowing the their slereachemistry CH3 H20215. Predict the product for the following reaction and 16. provide a stepwise, curved arrow, mechanism for the formation of the product. CH3OH H₂SO4 || = ||| IV ABCD A. B. C. Which of the following reactions would not yield propyl butanoate as major product? ===> OH NH₂ LOH H₂SO4 OH pyridine OH OH H₂SO4Match each reaction to a product. Answers may be repeated. Assume any necessary workup. Chiral products are racemic. D stands for deuterium, an isotope of hydrogen. OH a. b. OH d. e. not a.-d. NABD, Choose. BD3 NaOOH Choose.