Draw the structures for each of the intermediates in the boxes provided for the synthesis below. 004 HNO F HO CHCO) D Dydre R.SO. 1.1 NO fe HO H.SO. 2. CC1 NOH HO MCL HNO, H.50.
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- The bromination of 2-butene is an exergonic reaction. Br H3C. H;C. Br, CH3 CH3 Br a. Draw the mechanism for the reaction (you may ignore the stereochemistry for this question). 2.6. Provide the product for each of the following reaction. Indicate the type of reaction based on the reaction conditions. Show the complete mechanism for each reaction. Show the energy diagram for the reaction. F3C. CH3 CH3OH 25 °CAnswer all questions please with as much detail as possible!
- None027 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. +Identify the reaction sequence that will make the compound below from benzene. & 01. Br 0 CIN, AICI3 2. Br2, FeBr3 01. Br₂, FeBr3 2. ai AICI 3 , AICI 3 2. Zn(Hg), HCI 3. Br2, FeBr3 i AICI3 2. Br₂, FeBrs 3. Zn(Hg), HCI
- Identify (draw the structure) of the missing reactants or major product in the following transformations.Draw structure of substitution product(s) & major elimination productochem help... What is the product for the following three-step reaction sequence? Also, provide the structures or the major organic compounds formed in steps 1 and 2. (see attached image)
- Q7: For the following reactions, indicate the reaction conditions that would provide the indicated product in a high yield. Note the major reaction pathway that would take place (SN1, SN2, E1, or E2) Note: There may be other products that are not shown. There maybe more than one plausible pathway. Br H3C OH H3C CI ... H3C SCH2CH3 CI i SCH2CH3 ཨ་ Br System Sett1c. What is the nucleophile in the following reaction? .Br CH;CO0 Na LO OCCH3 NaBr ld. What is the electrophile in the following reaction? Br CH;COO Na L0OCCH3 NaBr +Which conditions will most efficiently affect the transformation shown? HO A) PCC B) 1. LiAlH4, 2. H₂O+ C) CrO₂, H₂SO4 D) 1. CH,MgCl, 2. H₂O+ OH
