What prpduct would you expect from the reaction of cyclopentene with NBS and water? show the stereochemistry? Please draw up the reaction and all the chemistry formed.
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What prpduct would you expect from the reaction of cyclopentene with NBS and water? show the stereochemistry?
Please draw up the reaction and all the chemistry formed.
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- Treatment of propylbenzene with NBS + hv affords a single constitutional isomer. Suggest a structure for the product and a reason for its formation.a. What is the major product obtained from the reaction of propene and Br2 plus excess Cl-? b. Indicate the relative amounts of the stereoisomers that are obtained.Drawing on what you know about the stereochemistry of alkene addition reactions, a. write the mechanism for the reaction of 2-butyne with one equivalent of Br2. A. predict the configuration of the product of the reaction.
- Drawing on what you know about the stereochemistry of alkene addition reactions, a. write the mechanism for the reaction of 2-butyne with one equivalent of Br2. b. predict the configuration of the product of the reaction.Give the balanced equations of the reaction of hexene/cyclohexene with the following in: • dilute KMnO4 • combustionWhat would be the expected major product when cyclooctene reacts with Cl2 in aqueous solution with H2O as the solvent?
- what are the reagents used to covert butane into (e)-2-butene and then into C4H8O? How would C4H8O be structured?What organic product is formed when 1‑methylcyclopentene is treated with NMMO in the presence of H2O and a catalytic amound of OsO4? Clearly show stereochemistry by drawing a wedge and dashed bond for each chiral carbon. Only draw one stereoisomer if more than one can be formed.Chlorobenzene give reaction with kmno4 or not??
- A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactionsWrite out all the isomers of the compound with molecular formula C4H10O . Select the normal/ primaryisomer and treat it with conc. H2SO4 and heat. Identify the reaction and give the product ‘A’ from it. 2. When ‘A’ is treated with HBr in the presence of a peroxide, give the name and structure of the product.The bicyclic alkene P can be prepared by thermal electrocyclic ring closure from cyclodecadiene Q or by photochemical electrocyclic ring closure from cyclodecadiene R. Draw the structures of Q and R, and indicate the stereochemistry of the process by which each reaction occurs.