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- 3. 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 NaOH18. Draw a reasonable mechanism and product(s) of the following E1 reaction. CH3NH₂ ElDraw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore any inorganic byproducts. H CH3 H Br Ph CH2CH3 NaNha M
- SN1 reactions undergo carbocation rearrangements, but E1 reactions do not because the carbocation intermediate does not last as long during the elimination process. True O FalseTertiary alkyl halides will react by E2 under neutral conditions under acidic conditions under basic conditions will not react by E2Draw the product of the E2 reaction shown below. Include all lone pairs. Ignore byproducts. :Br: I I I I I 00: :O-CH3 CH3OH heat Select to Draw the E2 Product I
- Ⓒ What is the major product of the following E2 reaction? >? LiTMP --B2 E2 م عامل های مترDraw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore any inorganic byproducts. H CH3 H Br NaNH2 Ph CH2CH3 ك5) Only one product is observed in this reaction. Draw the product and briefly explain why. Hint: It is NOT due to the Zaitsev rule. H3PO4 OH H₂O
