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- For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Which of the alkyl halide bromide below is/are capable of reacting by E2 elimination?Make an experimental step-by-step procedure with regards to the synthesis of Butyl Acetate shown below. Please make it detailed and tell the equipment used in the process. Thank you!
- In greater details, give at least one method you can use to idonate benzene?Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following question. Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed. The attached image contains the schemeFind the products for these two reactions. Make sure to include relevant hydrogens, deuteriums and stereohemistry.
- Bringing together your knowledge of the reaction chemistry of substituted benzenes, suggest a preparative route for conversion of compound A to compound B shown belowOutline a multi-step laboratory synthesis of the target shown below starting from indicated moleculesI need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important！！devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis
- Under basic conditions, the following substrates can undergo a [4+2] cycloaddition with regio- anddiastereo- control. Rationalize mechanistically how the reaction occurs as well as the regio- and stereochemical outcome with each base.Draw two complete elimination reactions including mechanisms (Zaitsev and Hoffman products) of 2 - fluoro-2-methylpentane. Indicate the reaction productsand provide the detailed justification regarding which reagents (bases) you chose for each product and why.Write a essay summarizing details and analysis of proofs for identification test for Qualitative Tests for carbonyls and Unknown carbonyl resulting in the finalUnknown, which is benzaldehyde.