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![Write a detailed mechanism for the following reaction.
OEt
H'
OEt
2 EIOH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa4390ff9-be31-4b08-a24a-9b9fb60c73a7%2F269d9bbd-a473-4236-a774-90f89a4f3aa7%2Ffqd9t96_processed.jpeg&w=3840&q=75)
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- Complete the following reaction with mechanism and a major product: O₂N- -CHCO₂Et CO₂Et PhCH₂Cl K₂CO3Draw the mechanism for the following reaction: conc. H,SO4 Нat (c) "OH Practice Problem 07.69b1 Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. H CH3 CH3 CH3 -CH3 + H H. OH Edit DrawingDraw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO
- NH 1) xs Mel 2) Ag2O, H2O, A 2. Complete the following reaction. Show the intermediate, and propose a mechanism for the second step.Draw the mechanism for the reaction of an alkyl halide with sodium azide followed by reduction. Complete the mechanism of the initial step of the reaction, then identify the key intermediate and the product. Step 1: Draw curved arrows. o z + Na + || : z: I Step 2: Complete the intermediate. Na +For the following reaction predict the major product and draw the complete mechanism including the mechanism for the electrophile formation. CF 3 H₂SO4 HNO3
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