Problem 3: Which alkene would be used to produce the following ? a) Bromocyclopentane b)1-Ethyl-1-iodocyclohexane Br Cl (c) CH3CH,CHCH,CH,CH3 (d)
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- What is major product choose from A, B, C, D , EFrom what alkenes might the following alcohols have been prepared?Compound A has the formula C10HI6. On catalytic hydrogenation over palladium, it reacts with only 1 molar equivalent of H2. Compound A also undergoes reaction with ozone, followed by zinc treatment, to yield a symmetrical diketone, B (C10H16O2). (a) How many rings does A have? (b) What are the structures of A and B? (c) Write the reactions.
- Problem 2: Consider the following reaction. Using mechanism and less than 30 words explain the outcome of this reaction.OChem Help... 1. Draw Fischer projection formulas for ALL steroisomers of 2,3-dimethyl-3-hexanol, giving sterochemical details for each structure. 2. What is the product(s) formed by treating 3,3 dimethyl-1-cyclopentene with Hg(OAc)2 in THF/water followed by treatment with NaBH4 in NaOH(aq)?Problem 4.13 Of the isomeric C5H11^+ carbocations, which one is the most stable?
- show how (s)-4-methylpentan-2-ol can be converted into (s)-2-chloro-4-mehtylpentane thank you18. Which of the following reactions from the products shown? Choose all correct answers.Problem 2. Synthetic Transformations Isobutyl alcohol (2-methyl-1-propanol), (CH3)2CHCH2OH, can be transformed to each of the compounds (1 through 12) listed in the left-hand column. In each case the number of steps needed to accomplish the change is noted, and an answer box is provided for your reagent selections. Fourteen reagents (designated A through N) are listed in the right-hand column.Enter letters designating the reagent or reagents you believe will achieve the desired transformation in the box to the right of the product formula. In the case of a multi-step sequence enter the reagents in the order they are to be used. In some cases you may wish to use a previously prepared compound as a reactant. If so, enter the number (1 to 12) corresponding to the desired compound
- For each reaction below, provide the product(s) that would form and indicate whether the substitution reaction would occur by an SN1 , SN2, E1, or E2 mechanism. Draw all constitutional and/or stereoisomers that would form in each reaction. I need help with this practice problem, thank you!Draw the major organic product of each reaction. Indicate the stereochemistry a. Draw product 1. If the C−OC−O bond breaks, assume inversion of configuration. b. Draw product 2.Tho following cycloalkene gives a mixture of two alcohols on hydroboration followed by oxidation. Draw the structures of both, and explain the result.