Predict which of the following carbocations will undergo rearrangement. For those that will rearrange, show the rearranged structure. For those that don't rearrange, explain why. +
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- . Use to curved arrow notation, propose a mechanism for the following reaction and state whether it is either SN1, E1, SN2, or E2. Give the IUPAC names of all organic reactants and products.Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the resulting structures in each step Step 1 of hydration of 2-methyl-1-propene (Note that the most stable carbocation is formed here) Step 2 of hydration of 2-methyl-1-propene(Note that the most stable carbocation is formed here) Step 3 of hydration of 2-methyl-1-propeneDraw the structure of the product of each step in the three-step synthesis. Show the formal charges, if applicable. As a start, the benzene ring is drawn for you in each product. Although the first step produces a mixture of isomers, the para isomer is isolated as the sole product of interest and used in the second step. Give only the major product for the second and third steps. Br₂ FeBr HNO3 H2SO4 Br₂. FeBra Product 1 Product 2 Product 3 (para isomer) Draw product 1. Select Draw Templates More с H Br Draw product 2. Erase Select Draw Templates More c Q2Q Draw product 3. Select Draw Templates More с H N о Br Erase c Q2 Q + CH N о Br Erase QQQ
- 2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and explain why it's unusual. SCH3 HBr Br SCH3 EN Please be sure to include all structures (use line angle notation or perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermediates, transition states, curved arrows, formal charges, or lone pairs as necessary. Please redraw the substrateIdentify the two diastereomeric hydroboration-oxidation products that can be formed from the following alkene by dragging the product pair to the product bin. Then suggest which product should be the major product or whether they will be formed in equal amounts by dragging the appropriate label to the bin under the products. Note: If one or more labels are incorrectly placed, a single red X will appear on the top left. 1) ВНз, ТHF 2) H-Ог. - ОН он Н Oн Н HI OH Н Он H ОН Н Он H Он Он. Н ОН Он ОН OH major praduct minor product minor product major product approximately equal amountsiPredict the structure of the product of each of these reactions. If no reaction occurs write NR andexplain.
- Arrange the following carbocations in order from least to most stable. First, expand the structures to show all of the carbon and hydrogen atoms, at least in the vicinity of the charge. +For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structures of the minor and major products of the elimination.Determine if the carbocation below is expected to undergo a rearrangement. Write NR if norearrangement will occur. If a rearrangement is expected, write the type of shift above the arrow,show the mechanism, and draw the resulting structure from the expected rearrangement.
