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- The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Arrange the following according to INCREASING reactivity towards E2: 1st ( least reactive)? 2nd? 3rd? 4th (most reactive)?Which of the following undergoes SN1 reaction at the fastest rate? Explain.
- please explain clearly and in detail. thank you! 2-butene reacts with NBS yields and forms two products, 1-bromobut-2-ene and 3-bromobut-1-ene. explain how this happens using mechanisms.Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)Please Answer the following question with proper explanation and mechanism with Chemdraw!
- what mechanism is involved? SN1, E2, E1, or SN2Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2The substitution reaction below forms two ethers (which are consitutional isomers). Which ether is the major product and why?
- Show the detailed mechanism of this in 3D structure, and predict the major regioisomer and the major stereoisomer with a stepwise explanation. show the final major product in Newman projection.Rank the following compounds in order of their expected reactivity towardSN2 reactions and explain your order. CH3Br, CH3OToS, CH3CCl, CH3CHClHello. Kindly help me understand if this is a possible schematic of the reaction. The specific question is in Organic Chemistry Principles and Mechanisms by Joel Karty 2nd Edition, Problem 12.11 on page 614. I believe the predicted major product should come as well as with its enantiomer hence 4 products predicted for this reaction as there is no easy rotation about the cyclic structure