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- Devise synthetic schemes for the following reactionPropose a detailed curved-arrow mechanism for the following transformation. Thank you!Be sure to answer all parts. Draw all constitutional isomers formed in the E2 reaction below and predict the major product using the Zaitsev rule. OH The tetrasubstituted product is: draw structure . The trisubstituted product is: draw structure.. The disubstituted product is: draw structure. The major product is the (select) substituted product.
- 9) Provide a synthesis for the given product with the starting materials below, be sure to account for the stereochemistry of the epoxide. OTMS Starting Materials ProductPropose an efficient synthesis of (C) and (D) of the following transformations1 Complete the following reaction scheme. Give all product(s) and indicate major or minor and any relevant stereochemistry.
- The following compound has extra stability in its enol form. Explain the reason that may lead to this extra stability and show by drawing the relevant structure. & CH3 CH3Propose a detailed mechanism for the following conversion4. Give the structure of compounds A to E in the following reaction sequence.