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- Based on the following seven-step synthetic scheme, answer the questions below. Indicate, in the schematic, the reagents you would use in each are available in the following inventory reagents from an FDA lab. NaCl, CH3OH, terbutanol, K, Na, K2SO4, THF, TsCl, NaOCH3, B2H6, H2O, H3PO4 85%, H2O2, H2O nanopura, PCC, K2Cr2O7, H2SO4, Mg, CH3Br, Cl2, NaOH, HBr 5%, HBr conc., fenolftaleína, dextrina, NaF, KMnO4, HCl 1%, CaCO3, C2H2, C6H6, H2, Pt, CCl4In a paragraph form, provide the experimental procedures of The second stage is the 3-benzoylpropionic acid reaction of Clemmenson, which results in 4-phenyl butanoic acid. Clemmensen reaction is observed in the presence of zinc amalgam and hydrochloric acid.please quickly thanks ! 3.Please write out the major reaction and side-reaction in the preparation of ter-butyl.chloride, and write out the key points to use separation funnel in this process.
- ANSWER ASAP Please show the electron-flow mechanism of nitrobenzene to aniline. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.PLEASE, I DO NOT UNDERSTAND IT, AND NOTHING IS HELPING. STEPS LEADING TO THE CORRECT ANSWER WOULD BE HELPFUL! BOND LINE DRAWINGS FOR ALL 5 PLEASE. Question: Draw the missing products or reagants in the following multistep synthesis. Ignore any inorganic byproducts.Synthesis of 3-Methylbutyl Ethanoate by an Acid Catalysed Esterification (FischerEsterification) & Purification by Simple Distillation Can you explain the details of what's going on this reaction please Specifics please i'll also leave a good review if you can help thank you
- 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).Question #16a. Please provide the missing reactants, reagents, or products for the following reaction sequences below. If a sequence leads to a race mic mixture you should indicate +enantiomer.- 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.
- 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!The sodium iodide test is used to identify primary alkyl halides and it also takes place via a substitution reaction.Describe the test including the reactions that explain the full mechanism. Explain whether this reaction follows aSN1 or a SN2 mechanism.Is the reaction shown a valid method to synthesize phenylacetylene from benzene and acetylene? Explain why or why not.