2. Provide a complete retrosynthetic analysis and a complete forward synthetic scheme to make the following target molecule from the given starting material. You may use any other reagents necessary. Br
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- (a) Provide a synthesis for the target molecule. All the carbons in your target must come from methyl acetate. H3C OCH3 methyl acetate Target (b) Provide a second synthesis of the same target that does not use LDA (iPr₂NLi) or an equivalent reagent.Please don't provide handwritten solution ...From naphthalene and any other organic or inorganic reagent synthesize the following molecule.
- 4. Provide a retrosynthetic analysis and forward synthesis for the following molecule. (Provide the reagents to carry out the following reactionQ6 Complete the retrosynthetic analysis. Supply all reagents and precursors, for both parts: A and B. Fewest possible reaction paths should be choiun. Part A V Part B Mi
- Provide step by step total synthesis of the following target compounds using the starting material provided.Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from the given starting material (on the right). (any reagents maybe usedPlease don't provide handwrittin solution....
- US 4. Provide a synthetic route / strategy, leading to the synthesis of compound (D) via electrophilic aromatic substitution (EAS). (D) CH2CH3 CH2CH3Give clear handwritten answer with explanation needed..please explainWhich reagents can be used to achieve synthesis of the indicated target molecule? Conc. KMNO4/ H* / acetone 1) O3/ Zn/H* 2) PCC/CH2Cl2 O 1) Conc. KMNO4 /H* 2) LIAIH4/THF 4) H3O* 1) Conc. KMNO4, 2) HBr, 3) Mg/ether, 4) CO2 O3/ Zn/H*