is) Using retrosynthetic analysis, provide a synthesis for the reagents next to the arrows and the necessary intermediate in the box provided. 1. 2. MeO 0 NH 1. 2. 23 3. MeO OMe
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- Which of the following are a major product of the reaction sequence shown belo (1) Br2, FeBr3 (2) Mg/ether он он (A) (B) (3) (4) dil H* /H;O (C) (D) он Compound C Compounds B and D OCompounds A and B Compound D1) Provide a synthesis for the product shown below given the starting material. ? OMeRetrosynthesis For each of the following, perform a retrosynthetic analysis and then design a synthesis to go from the reactant(s) to the product(s). You are free to use any reagents or reactants as long as the listed reactant is incorporated or unless otherwise specified. 15) Synthesize: From:
- please answer both, will rate. 24) What is the product of the following reaction? C6H5CO₂Et + CH3CH₂CO₂Et A) CH,CCH₂CH₂COET 00 || B) CH,CCHCOÉt A) B) CH3 A) A O A) A B) B c)C. D) D 25) Which of the following is the conjugate base of ethyl butanoate? :0 B) B C) C 0 0 C) CH₂CH₂COCC6H5 (1) NaOCH₂CH3 (2) H₂0* 00 D) CH₂CHCOCC Hs CH3 C) D) el D) DProvide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. Please include both a retrosynthesis and a forward synthesis (that includes the product and reagents of each individual step in your synthesis).(b) Show how to synthesize the molecule at right, using the molecule at left as a carbon source, plus any other reagents without restriction. KOH H₂ EtOH Pd/C
- 29. Provide a potential retro-synthesis of the following molecule in a detailed scheme. Label all steps, include all reagents and arrow pushing.provide both a retrosynthesis and a synthesis for the following molecule showing full steps and reaction mechanismsProvide the reagents to carry out the following reactions A. |–
- Provide a synthesis for the following molecule, starting from the given compound and any other reagents needed.Please provide the retrosynthetic analysis of the compounds below. Include the appropriate starting reagents and solvent use. Write a detail forward reaction scheme for the following synthesis OTwo possibilities for a Wittig synthesis of the compound below involve using: 1)cyclohexanone and ethyl bromide or 2) bromocyclohexane and ethanal. Is either routebetter, and if so, why is one superior? Be specific and explain where the difficulty lies forthe inferior route