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- 9. For the following carbocations: 1) determine if they rearrange, and 2) if they rearrange, draw the expected product and the curved arrows to complete the rearrangement.Draw the structure of the expected rearrangement product for eachwhy does this carbocation go through rearrangemnt by a hydride shift?
- Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. Do not include the halide anion. Let Marvin JS adjust the number of hydrogens automatically as you use the charge tool to specify formal charge. + HCI Marvin JS - Troubleshooting Marvin JS - Compatibility9. Predict whether each of the following carbocations will rearrange. If so, draw the expected rearrangement using a curved arrow, and draw the resulting carbocation. A. B. C.reaction of this alkene to the different reagents written above and below the arrows
- What other alkene is also formed along with Y in Sample Problem 9.3 (Attached) ? What alkenes would form from X if no carbocation rearrangement occurred?1. Draw the mechanism for the following reaction. Include all intermediates, formal charges, and arrows. ol CH3CH₂NH2 H*, -H₂O3. Draw all possible monobromination products (including stereoisomers) for the following molecule and circle the major product(s). II CI NBS hv
- at product will result from the reaction shown? (Just mention the class of compound not the nomenclature) CH3 HOCH,CH,OH CH;CHCH,CH,CH,C-H H+7. Draw the complete, detailed mechanism (curved arrows) for each of the following reactions occurring under SN1 conditions and under SN2 conditions. Pay attention to the stereochemistry of the product. al + SN1 mechanism SN2 mechanism Br SN1 mechanism + KBr SN2 mechanism NaOH CI + NaOCH3 SN1 mechanism SN2 mechanismRank the following carbocation in order of increasing stability?