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starting with ethyl acetoacetate and formaldehyde as your only source of carbons synthesize the following
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- Synthesize the following compound from cyclohexanone and any other organic and inorganic reagents you need.Propose a step-by-step mechanism AND the products for the following reactions.Synthesize the following syntheses starting from the starting compounds using the necessary organic and inorganic reagents.
- The following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium acetate, the protonated form of pyrrolidine. Draw the product of this reaction, assuming that a dehydration reaction takes place.What reagents are required to carry out the following synthesis?Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexene
- Propose a synthesis for the following compound start with any reagents with four carbons or fewer.Complete the following multistep syntheses by showing the major products and the reagents nessesary for each stepShow how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents.
- Synthesize the products shown below starting from the reactants provided and using any other necessary reagents. Clearly draw out all reagents and intermediates on the pathway to the product.What is the series of reactions for the following synthesis?Complete the following multi step synthesis by showing the major intermediate products and the reagents nessesary for each step