Complete Assignment M3.4 Use a sheet of paper to answer the following question. Take a picture...
Use a sheet of paper to answer the following question When complete, take a picture of your answer and attach the file to this assignment. The reaction of (2S)-2-chloro-3-methylpentane with sodium iodide yields two products: () 2R)-2-iodo-3- methylpentane, (2) racemic 3-iodo-2-methylpentane. Draw mechanisms to account for the formation of each of these products, giving explanations to support your mechanistic rationale.
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment Draw an isomer of dibromocyclopropane that has (a) one proton environment; (b) two proton environments; (c) three proton environments.
Complete Assignment M 6.2.2 Use a sheet of paper to answer the following question. When complete, take a picture of your answer and attach the file to this assignment. The reaction of (25)-2-chloro-3-methylpentane with sodium iodide yields two products: (2R)-2-iodo-3-methylpentane and racemic 3-iodo-2- methylpentane. Account for the formation of each of these two products. For each product, you should show how it is formed and what that tells you about the mechanism of that specific reaction.
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment The 'H-NMR spectrum of 1-bromopropane shows three signals and the 'H-NMR spectrum of 2- bromopropane shows two signals. Draw these two molecules and determine the relative integrals of each signal.
Complete Assignment M 2.10.6 Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. There are several isomeric alcohols and ethers of molecular formula C5H120. Two of these exhibit the following 'H-NMR spectra. Propose a structure for each of the isomers. Isomer A: 5 = 0.92 (t, 7.8 Hz, 3 H), 1.20 (s, 6H), 1.49 (q, 7.8 Hz, 2H), 1.85 (s, 1H) ppm Isomer B: 5 = 1.19 (s,...
Use a sheet of paper to answer the following question. Take a picture of your answers, insert the image into a Word Doc and attach below. (R)-3-Bromo-3-methylhexane loses its optical activity when dissolved in nitromethane, a highly polar but non-nucleophilic solvent. Explain this observation by providing a detailed mechanism.
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. There are several isomeric alcohols and ethers of molecular formula CsH20. Two of these exhibit the following 'H-NMR spectra. Propose a structure for each of the isomers. Isomer A: 8 = 0.92 (t 7.8 Hz. 3 H). 1.20 (s, 6H), 1.49 (9,7.8 Hz, 2H), 1.85 (s, 1H) ppm Isomer B: 8 - 1.19 (s. 9 H), 3.21 (s, 3H)...
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. From what aldehyde or ketone could each of the following be prepared by reduction with NaBH4 or LiAlH4? ОН То маягаар ОН .. "n h.mic. дело. В , За да се каад ... ... Ek.k React... печат ел- . . тату - - Antarask start а за у, те . ... .. ... тут .. . ...Зам. А ая,...
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. Compound 1 has molecular formula C6H12. It shows three signals in the 1H-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Compound 2 has molecular formula C7H15Br. It shows two signals in the 1H-NMR spectrum, one at 1.08 ppm and...
Use a sheet of paper to answer the following question: Take a picture of your answers and attach to this assignment. Compound 1 has molecular formula CH 12. It shows three signals in the TH-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Compound 2 has molecular formula CH1Br. It shows two signals in the 'H-NMR spectrum, one at 1.08 ppm...