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- in this E2 reaction what is the major productWhich reaction can be used to carry out the following transformation? A. B. 1. AICI 3 AIC13 2. HCI, Zn(Hg) C. Either is okay D. Neither will workSECTION 6: Show the mechanism of each reactions with arrows and intermediates form as in a. b. C. HBr Br₂ Cl₂, H₂O Br Br CI Br OH
- 4. Circle the electrophilic and nucleophilic atoms in each substitution reaction below. Provide the neutral organic product; where a stereocenter is created, use a wavy bond to indicate a mixture of configurations or wedges/dashes for stereospecific reactions. Also, provide the dominant reaction mechanism (Sn2 or SN1) somewhere in each box. A. Br NaSEt DMF В. ELOH C. .SO2NHNA Cl + D. NaH Br- HO, DMFThe 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.Can someone show a detailed reaction mechanism for this problem?
- Provide the missing intermediates and final product in the following synthesis. 1. LDA (excess). A 2. Н,о Br2 1. NaH В 2. C H,/Pd CI4 Lindlar catalyst ВА 1. CH,MgBr H,CrO4 D E 2. NH,CI, H,O F G3. Draw the reaction mechanism for the following reactions. When possible, label nucleophiles/electrophiles, carbocations, and oxonium ions. H* CI. a) H. + H2O + НОCHЗ H* OH H* H;CDo it clearly...