Provide the reagents that would complete the synthesis below. Me Me, Me Me HO. "Me но Me Ме 'CI Type your steps and reagents in as your answer. Example: 1. PhMgBr, THF 2. H20, HCI 3. PCC, DCM 4. NABH4, MeOH
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- Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final product-Reactions E1 and E2 with AlcoholsIt develops the following reaction mechanisms and the main and secondary products:Give the reagents necessary for the synthesis above and please show the detailed step-by-step mechanism.
- 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).Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Give the products of the reaction given below and state which reaction willproceed faster?
- Provide the major organic product of the reaction below and a detailed, stepwise mechanisProvide the missing reagents to complete the reactions below, if there is more than one step required, be sure to indicate appropriately.Any help with these would be great! Thanks in advance:) What is the major product of the reactions?