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- Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.For SN2 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.can you explain to me how to work this problem step by step please thanks
- PLEASE, I DO NOT UNDERSTAND IT, AND NOTHING IS HELPING. STEPS LEADING TO THE CORRECT ANSWER WOULD BE HELPFUL! BOND LINE DRAWINGS FOR ALL 5 PLEASE. Question: Draw the missing products or reagants in the following multistep synthesis. Ignore any inorganic byproducts.Predict the organic product for the reaction and complete the arrow pushing mechanism. Please use the steps that are given, this would be incredibly helpful.Fill in the missing starting material, reagant, or product where neccessary.
- Please clearly draw the overall reaction taking place between methyl salicylate and sodium hydroxide. Be sure to include all reagents and by-products. Show the mechansim as well.The question is: "Draw the curved arrow mechanism for the reaction between (2S,3S)-3-methylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms" I attached screenshots of the picture of the atoms below. What type of reaction (SN1, E1, SN2, or E2) would the reaction be, and how would these molecules interact? The question asks for multiple steps so I am guessing it is either SN1 or E1, but what is the reaction mechanism?Could you please help me with this question? The reaction shown below does not follow the expected theory. Given what you learned about substitution/elimination, what is the expected mechanism this reaction should follow? Suggest why that is not what happens and give the actual product of the reaction.