G 5% Carbocation Rearrangements 7) Draw the 5 MOST LIKELY carbocation rearrangements of the following intermediate. Bonus: Put an X next to the least likely structure and briefly explain why. alk of
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- Which of the given reactions would form meso product? H₂O, H2SO4 III m CH3 CH₂ONa CH3OH || H₂O, H2SO4 CH3 1. LiAlH4, THF 2. H₂O CH3 IV2. Draw the carbocation intermediates (if any exist) and the products for each reaction. Include any intermediates and products arising from carbocation rearrangements. Be sure to include stereochemistry!!! 1. ВНз 2. Н2О2, NaOн H2SO4 H20 Br2 HO. H2SO4 HOʻWhat reaction out of each pair is faster?????
- In the E2 reaction of 2-bromopentane with sodium tert-butoxide, 1-pentene is favored over 2- pentene. It is based on O the size of base used. O the Zaisev's rule. O the strength of the base used. O the Hoffman product. O the stability of alkeneDraw the major organic product for each of the hydroboration-oxidation reactions. Disregard stereochemistry. Draw the product of Reaction A. Select Draw Rings More ||||||CH|OB Reaction A. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH Reaction B. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH S 3 Draw the product in reaction B. Select Draw Rings More |||||||||CH|OB Erase Q2Q Erase Q2QIn the first box, draw the tetrahedral intermediate involved in this reaction.In the second box, draw the product of the reaction.Include all lone pairs of electrons and nonzero formal charges. Do not add curved arrows.
- draw the product for both reactions...Draw the structure of the major organic product of the following reaction. CH3 CH3CHC=CH2 1. Hg(OAc)2, H₂O 2. NaBH4 CH2CH3 • You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. 44494 ? [F Skip question ExitThe resonance stabilized carbocation formed in step one has two electrophilic centers draw. The final step of the mechanism is in both provided resonance structures.