Draw the major organic product generated in the reaction below. Pay particular attention to 1) regio- and stereochemical detail. CH3. -CH3 KMN04 (warm, conc.) CH3 H
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- draw the major organic product generated in the reaction below. Pay attention to Regio and stereochemical detailAssign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).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).
- Please complete all these reactions in handwritten! I will upvote you!The molecules below react in a displacement reaction. Determine the products) and assign configuration (R/S) to any stereogenic centers in the product. The Cahn-Ingold - Prelog rules can be used to assign priority to the four different groups on a stereogenic center.For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
- (a) A compound known to be a substituted cyclohexanone derivative has lamda max of 235 nm. Could this compound be a conjugated dienone? explain (b) (i)For this compound, how many nm must be accounted for by substituents? (ii) What are the substituents and the points of substitution that may occur having accounted for the 20nm?2. In not more than three (3) sentences, explain why terminal alkynes are acidic.3. What impurities are removed when acetylene gas is made to pass through an acidifiedsolution of CuSO4?4. Explain the difference in the rate of free radical bromination reactions of toluene and cyclohexane.b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bondcleavage and bond formation.
- Nitrating methyl benzoate. 1.Describe the mechanism of EAS clearly and in detail 2. What is the effect of subtituent of the outcome of EAS;include 3 classes of subtituentsFor each reaction shown, determine which substitution mechanism (SN1 or SN2) is likeliest to predominate, and provide two reasons to support your answer.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.