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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- Provide a retrosynthetic analysis and forward synthesis for the compound shown below. H- and any other reagent of one carbon or less.(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.Provide a synthesis for the following transformation.
- Please don't provide handwritten solution ...Draw the reaction scheme. Use one arrow direct from starting materials to products.Provide the reagents necessary to carry out the following conversion using a Stork enamine synthesis. O LO -O; H3O+ CH3NH/H₂SO4; NaOCH 3; (CH3)2NH/H2SO4; (CH3)2NH/H2SO4; CH3NH/H₂SO4; =O; H3O+ =O; H3O+ -O; H3O+ FO; H3O+
- A) Suggest two possible syntheses for the following target molecule (TM), starting with any aldehyde (start each synthesis with a different aldehyde). It may help to first consider a retrosynthesis of the TM. он CH3. CH-C-CH2CH2CH2CH3 CH3 Hint! Possible aldehyde starting materials: тв для Ph TMProvide the retrosynthetic analysis and synthetic route for the following Compound.4. Provide a retrosynthetic analysis and forward synthesis for the following molecule. (
- 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....