2. Starting with any alcohols (≤4C) and any inorganic reagents required make the target molecule. Show the retrosynthesis (show synthons only when breaking C-C bonds) and synthesis. retrosynthesis: TM OCH,
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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).1-Complete the reaction in the first picture. 2-Show the synthesis of ethyl propyl ether by using suitable reagents via Williamson ether synthesis?.The name for Reaction 1 is _______ Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation The reagent/s for REACTION 1 is/are ______ Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromide
- Starting with any alcohols (SIC) and any inorganic reagents required make the target molecule. Show the retrosynthesis (show synthons only when breaking C-c bonds) and synthesis.Propose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)Please give the appropriate reagents FOR 3 and 4 to complete the following synthesis. ******** Keep mind, H2/PD does NOT go into 3 and KMNO4 does NOT
- Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.What is reaction 1 and 2 called? Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation What are the reagents for reaction 1 and 2? Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromideProvide a retrosynthesis (with complete reaction conditions) of the followingcompound from alkyl halides containing 6 carbons or less. The starting materials may be any type of alkyl halide (primary, secondary, or tertiary). You may use any other reagents you find necessary.
- I 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 synthesisCould you please help with synthesis and a retrosynthesis for each of the attached. Need to show reagents and intermediate structures?The name for Reaction 1 is _____ while Reaction 2 is called _____. Choices: A. Williamson Ether synthesis, B. Hydration, C. Epoxidation, D. Acidic cleavage The reagent/s for REACTION 1 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. H2O/H3PO4, C. H3O+, D. HI The reagent/s for REACTION 2 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. water in acidic medium, C. dilute acid, D. hydroiodic acid