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- Attached compounds undergoes E2 elimination with strongbase? For compounds that undergo elimination, draw the product. Forcompounds that do not undergo elimination, explain why they are unreactive.What is the best way to remeber the differences between Sn1, Sn2, E1 and E2 reations?Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2
- Attached compounds undergoes E2 elimination with strongbase? For compounds that undergo elimination, draw the product. Forcompounds that do not undergo elimination, explain why they areunreactive.Draw the major product and state wheter the reaction is SN2, E2, SN1, or E1Using resonance structures of the intermediates, explain why bromination of biphenyl occurs at ortho and para positions rather than at meta.
- Why is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + water1. Draw a reasonable arrow-pushing mechanism for the transformation shown along. 2. Identify nucleophiles and electrophiles 3. Name any type of reactions taking place like E2 or E1 4. Account for any regio- or stereoselectivityDraw the major product of this reaction. Ingore any organic byproducts