3. For the following reaction: NaOH DMSO ? a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism(s): d. predict the major organic product by drawing the appropriate mechanism:
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- 1. .CI HC C: Li HC CH LICI 2. -CH3 OH Aqueous HO-S- -CH3 acetone g = SN1 Nucleophilic substitution Electrophilic a = Proton transfer addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from the mechanisms listed. Use the letters a - i for your answers. among 1. 2.Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.1. Give the mechanism and the major product for the reactions below. a. CI 야!!! OH NaOH. EZONLY
- Synthesize the following compound from cyclohexanol using any other organic or inorganic compounds. HO. Part 1 out of 2 Preparation of the Grignard reagent: Book rint rences OH draw structure ... draw structure... Draw the intermediate product formed above and select the correct reagent A. O MgBr, O CH;Br O Brz PB13 Draw the intermediate product formed above and select the correct reagent B. O MgBr O Mgo O O Mgl, O Mg Hint Prev 3 of .8 Next > re to searchDraw the major organic product for each of the hydroboration-oxidation reactions. Disregard stereochemistry. Draw the product of Reaction A. Select Draw Rings More ||||||CH|OB Reaction A. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH Reaction B. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH S 3 Draw the product in reaction B. Select Draw Rings More |||||||||CH|OB Erase Q2Q Erase Q2QIdentify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН
- 1. 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 .... в027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +1. Consider the following reaction. CI EtOH OEt a. Provide a reasonable arrow-pushing mechanism for the following reaction, showing all steps and balancing all charges. b. Predict the stereochemistry of the final product(s). c. Label the electrophilic sites on the molecule and explain why only one of them undergoes substitution.