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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- Which of the following carbocations is (are) likely to undergo rearrangement through a hydride shift? CH2 CH3 CH:Payalben. 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-propene[Review Topica) Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown. [References) CH;CH2 H C=C HCI H. CH2CH(CH3)2 • You do not have to consider stereochemistry. • Do not include anionic counter-ions, e.g., I", in your answer. • For cases in which carbocations of the same or similar stability are expected, draw all of the structures. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. C P. opy aste ba 2req = 2req Previous Next Save and Exit APR MacBook Air DII 品留 F4 80 F9 F10 FS F3 & %23 $ %3D 3 4 5 6 8 9 { P E R т Y F G H J K L C V N command oprion -The following reaction conditions gives a mixture of two addition products A and B shown below. CI. HCI Ph Ph Ph Ph Ph A B via rearrangement via rearrangement >Draw< a clear mechanism using electron-flow arrows showing the formation of both products (A and B) from the starting materials. Transition states are not required and ignore the stereochemistry in this question. Do not use any other compounds in your answer except those given. Note that this is not a synthesis question. OYork rk.Unesk 020
- 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 substratePredict 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. +
