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- b).. .. Under each potential product of this E2 elimination, write "major product," "minor product," or "not formed." Me Br H Me Me OH Me Ph Ph H Me H Et Me Me Me Ph Ph Me Me Etla . Rank the following substrates from most (1) to least reactive (3) in an Sn2 reaction. Explain the reason for your choice Br Br Br В A lb. Rank the following substrates from most (1) to least reactive (4) in an SN1 reaction. Explain the reason for your choice Br Br Br Br A B C DWhat is the predicted major product of the reaction sequence shown? он KMпO,/NaOH/H20 1. NaOHЛ2 сH,ОН 2. H,O* H2SO4 CH3 III IV ОН OII OIV
- In the given reactions both E1 products went through carbocation rearrangements before elimination occurred. Does the mechanism in each reaction involve a hydride shift or a methyl shift? O Hold and drag to reorder 1. = Hydride shift 2. = Methyl shift = Hydride shift = Methyl shift Br CH,CH,OH 1) heat CH,CH,OH heat Br 2)How does doubling [B:] affect the rate of an E1 reaction?2. Complete the E1 reaction and answer the following questions. Cl Reagent: AH> 0 a. Draw a mechanism of the reaction above. Major El product: b. Draw an energy diagram of the reaction. Provide the structures of the starting material, intermediates, product, and all transition states.
- Draw the structure of the product of the reaction below. B 0 + 人 + H₂N.Draw the products of the two step reaction sequence shown below. Ignore inorganic byproducts. If the reaction results in a mixture of ortho and para isomers, draw only the para-product. HNO3 (1 equiv) cat. H2SO4 ✔ Please select a drawing or reagent from the question area3. Both El and E2 reactions are possible with 3° alkyl halides. Which elimination mechanism would be favored by the base NaOH? Show the curved arrow mechanism leading to both regioisomers. Draw the energy diagram for this reaction and include the transition state structure leading to each of the possible products. Indicate which one would be favored and use the energy diagram to explain your reasoning. How would you favor the other regioisomer? Br z odd NaOH