Synthesis. reagents, intermediates, >, provide the synthesis for the following transformation. You must include appropriate and formal charges.
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A: Please find the attachment.
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- Which of the following correctly describes a key step of the reaction shown in the box? 1. ELONA 2 2. HаО, НСІ OEt :o: :o: :o: A) Et H3C p: 1 :o: :o: :o: :o: B) H3C Et H3C :o: :o: :0: + C) H2C H3C :o: H :0: :0: :o: D) H3COEt H3C OEt O A O B OD O=24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IVDrow the next reaction product. (b) please!
- Part A Predict the product and propose a mechanism for the elimination reaction that results when (S)-(1-chloropropylibenzene, - CH, is heated in the presence of HOCH, CH,, Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron-fiow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H. BrShow all He steps necessay, inorder to make each of the followring compoundS, Starting with benzene Br BrOChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.
- of the molemles from the phato and draw a dedalled Pick a synthetic route to one pushing a proposed syntheses.(ie. you only need to show the mechanism arow mechanism CS) to erplein al Steps for one of the propsed syntheses of the disubsdituted benzene mole.cmles )Question 6. Predict the product of the following reaction and draw the mechanism. Includes all steps, including the formation of the electrophilic species if required, and justify your answer (substitution position) using resonance structures. CI AICI3A student proposed the following syntheses. Explain why they would notwork as written.