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Give evidence and prove that E2 reactions are predominantly anti-elimination, and there is a relation between conformation and reactivity.
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- Give evidence and prove that E2 reactions are predominantly anti-elimination.For this Sn1 reaction, why are there inversion? And are there any other stereochemistry consequences occurring? If you could please explain in detail, I would really appreciate it. Thank you!Explain the Summary of Alkyl Halides and SN1, SN2, E1, and E2 Mechanisms ?
- . Discuss the truth of the following statement. Explain why it is true or false Every SN1 reaction produces racemic mixtures in the productsConsider the following statement in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To which mechanism(s), if any, does the statement apply? Is greatly accelerated in protic solvents of increasing polarityConsider the following statement in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To which mechanism(s), if any, does the statement apply? Substitution at a stereocenter gives predominantly a racemic product
- Consider the following statement in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To which mechanism(s), if any, does the statement apply? Involves retention of configuration at the site of substitution.Consider the following statement in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To which mechanism(s), if any, does the statement apply? Involves inversion of configuration at the site of substitution.After E2 elimination, will the following molecule contain deuterium? Why or why not?
- 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 = Brady(i) Explain with the aid of a reaction mechanism why the synthesis is highly diastereoselective. (ii) Draw the structures of the enantiomer, and one epimer of J, and give definitions of these terms.Give detailed answer- Provide example of compound that fulfil each criteria below. Explain why-A)1,2-disconnectionB)1,4-disconnectionC)1,5-disconnectionD)1,6-disconnection