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- 2. Draw the product for following reacttons. Propose mechanism for each of reactions. a) DCIA student proposes the following reaction mechanism for the reaction in Model 6. Which step inthis mechanism is least favorable? Explain your reasoning.Draw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CI
- transformation. OH Major synthesis Mini synthesis Draw a synthetic scheme to perform the following LOHdraw the mechanism for all 3 steps Propose a plausible mechanism for the following transformation. This reaction will appear later in this chapter, so practicing the mechanism now will serve as preparation for the rest of this chapter. xs NH CI NH2 Step 0 Correct. These are not acidic conditions, so the mechanism begins with nucleophilic attack and has three steps overall: 1) nucleophilic attack, 2) loss of a leaving group, and 3) deprotonation. Identify the most likely sequence of steps in the mechanism. Deprotonation, followed by concerted Nucleophilic attack and Loss of a leaving group Deprotonation, Nucleophilic attack, Loss of a leaving group Nucleophilic attack, Loss of a leaving group, Deprotonation Concerted Nucleophilic attack and Loss of a leaving group, followed by Deprotonation Step 1 X Incorrect. 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. Use the +/- tools to…5. Glutaraldehyde is a germicidal agent that is sometimes used to sterilize medical equipment. In mildly acidic conditions, glutaraldehyde exists in a cylic form as shown below. Draw a stepwise detailed reaction mechanism for the reaction below. Но OH [H,o*) H. Glutaraldehyde
- Draw all the main products to the reactions. No mechanism needed. Thank you!Match each reaction sequence to a product below. Assume any necessary workup. Answers may be repeated.For the following reaction predict the major product and draw the complete mechanism including the mechanism for the electrophile formation. CF 3 H₂SO4 HNO3