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- You were told that is best to use a methyl halide or a primary alkyl halide for the reaction of an acetylide ion with an alkyl halide. Explain why this is so.Write the mechanism for the nucleophilic acyl substitution reaction in Figure 40.Write the mechanism for the nucleophilic acyl substitution reaction in Figure 40. Generate a SMILES -notation for the first reactive intermediate in the mechanism.
- Please answer questions 7 and 8 on the attached sheet. Please provide the major and any minor products for both the SN1 and E1 reactions and explain how they were calculated. Thank you.What can be the combination of reagents/conditions that could be in the box (step 9)What are the important mechanisms that should be highlighted in this image? How do they work together to create the final product?
- - The reaction that will be carried out in the lab will convert 9-fluorenol to 9-methoxy fluorene usinga nucleophilic substitution reaction. Question: Why is concentrated sulfuric acid used in this reaction and not aqueous acid? Draw the reaction and show the equilibrium that is dependent on the acid.Write the synthesis steps of the reaction given below.Write what products A, B, C, D and E were in the reactions below.
- In this experiment a reactive aromatic compound, acetanilide, will be brominated using molecular bromine (generated in situ from hydrobromic acid and potassium bromate) as the electrophilic reagent. Based on this information, please answer questions 2 and 3.The structure below represents a tetrahedral alkoxide-ion intermediate formed by addition of a nucleophile to a carboxylic acid derivative. Draw both the starting acid derivative and the ultimate carboxylic acid derivative product. Do not include the product formed by the leaving group.Please help me with the organic chemistry question below: 1) Show the mechanism for the linkage of two pyrroles with a benzaldehyde.