f) g) h) i) j) Br of CH3 H3C CH3 Br 1. NaOEt 2. H₂, Pd/C Hg(OAc) 2 H₂O, THF -C=C-CH3 -MgBr (xs) Na Ma Dry ether NaBH4 H3O+ H+ - H₂O NH3 (liq) D₂O
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Please solve parts f,g,h,i,j.
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- A student was given from the list of the compounds below A, B and D blindly and asked to identify them all. He treated each of them with Brady's reagent (2,4-ditrophenylhydrazine) and isolated a bright yellow compound for one of them, but the other two gave false negatives. The student reasoned that the false negatives may be due to sterics and, on further thinking, it dawned on him that he might be able to rule out one of the false negatives with the haloform test. What compound did he find compatible with the haloform test? That compound did indeed give a false negative in the Brady test. Which of the other two was positive in the Brady test? A = haloform B = Brady A = haloform D = Brady B = haloform A = Brady B = haloform D = Brady D = haloform A = Brady D = haloform B = BradyCan you assist with predicting the organic product(s) of the last two reactions and provide stereochemistry, if applicable.Give the major organic product(s) of the reaction shown below. Be sure to show all stereoisomers formed, and indicate which isomers are formed in equal and unequal quantities.
- 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).give the organic product/s of the following reactions (include stereochemistry where appropriate) , please help with all partsI 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
- 1. Give the major organic product(s) of the reaction and include all the stereochemistry as appropriate. Identify any meso compounds. 2. Indicate whether a solution of the product would be optically active or no not active and provide a simple reasoning to support your choice. Need the last 2Why does isopropyl benzene gives more para substitution without the cosolventGive only typing answer with explanation and conclusion What is the main product formed in the Friedel-Crafts alkylation reaction of benzene with 1-butene and AlCl3?
- Given the sequence of reactions shown below assume the reactions are stoichiometric fill in the reagents needed for steps A B and C and explain what happens in each step of the reactions, by also nameDraw the products formed by the following acid-base reaction without consideration of the equilibrium position: You do not have to consider stereochemistry. You should include all products. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Separate structures with + signs from the drop-down menu.Define Hemiacetal, Acetal and Ketal. ii. Give the structure of the product from the reaction of propanal with 1M ethanol in dry acid. iii. What happens when Further 1M of ethanol is added to above?