Draw the curved arrow notation and products for each elementary step described by the sequence shown here. Note: The products of each step should be used as reactants in the subsequent step. 1. Electrophilic addition of HO ? 2. 1,2-Methyl shift 3. Electrophile elimination of H®
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- From the following reactions couples Which of them will go faster ? ExplainDraw the curved arrow notation and products for the each elementary step described by the sequence shown here.Note that the products of the first step should be used as the reactants in the second step, and remember to click on each box to see step-specific instructions.Draw the mjor product of both question with mechanism asap
- Drawing the Product(s) of a Mechanistic Step. For the reactions that have TWO starting materials, indicate/label which species is the nucleophile and which isthe electrophile. Then, by following the curved electron-pushing arrows, draw the product(s) of the following reaction steps. Finally, identify and label what type of elementary step is represented for each mechanism.Draw the curved electron pushing arrow for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making stepsWhat reaction out of each pair is faster?????
- Sometimes carbocation rearrangements can change the size of a ring.Draw a stepwise, detailed mechanism for the attached reaction.Draw a detailed mechanism using curved arrow notation that leads to the formation of the pinacol rearrangement product shown below. (TsOH = H+)Which of the following would proceed with the fastest rate? Why? Options: top reaction due to stronger base bottom reaction due to stronger base top due to less hindered substrate bottom due to more hindered substrate
- The reaction shown here is an example of a deiodination. Without AlCl3 present, no reaction occurs. Draw a complete, detailed mechanism forthis reactionDraw the complete mechanism of each pair of reactants including any favorable rearrangements and all important resonance structures of all intermediates. a. Which reaction has a lower PE carbocation intermediate? b. Draw an energy diagram showing the reaction profiles of both reactions in the previous question. Use a dotted line for the first pair of reactants and a solid line for the second pair of reactants. (Assume the energy of the starting materials and products are the same for both pairs and the reactions are neither uphill nor downhill on net. c. Mark points on the energy diagram corresponding to each carbocation in your mechanisms.Draw the curved arrow notation and products for the each elementary step described by the sequence shown here.Note that the products of each step should be used as the reactants in the next step, and you may need to draw in additional reagents as directed.Remember to click on each box to see step-specific instructions.