Which reagent(s) would transform propyl alcohol into propyl bromide? A. Concentrated HBr and heat. B. PBr3 C. NaBr/H₂O and heat D. answers A and B E. All will accomplish this transformation.
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Give detailed mechanism Solution with explanation needed..don't give Handwritten answer...
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- What would the final product look like? What regents and or solvents/temperature belong above and below the arrows. Draw the final product of the third step after treatment with KMnO4, KOH, and heat followed by aqueous acidic workup.What would the final products look like? Pls specify stereochemistry if needed
- a) Write a description of the compounds involved in the synthesis (functional groups, specific features). b) Describe the steps involved in the synthesis and the role of each step. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis.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 synthesisAnswer all questions. ai. Give the structure of the product formed from the reaction of propanal with 1M ethanol in dry acid. ii. What happens when Further 1M of ethanol is added to the reaction in i above?
- 1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above 2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10 3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above 4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2 5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the aboveFor 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).Find the products for these two reactions. Make sure to include relevant hydrogens, deuteriums and stereohemistry.
- Draw the main organic products of the reaction. Indicate the stereochemistry, including all hydrogen atoms, at each stereocenter. Omit byproducts such as salts or methanol.The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Fill in the missing reactants, reagents and products. Include the stereochemistry if necessary. Unless otherwise stated, assume the reagents are in excess.