What is the most likely product distribution for the reaction shown below? Na HS Br DMSO SH C S Compounds B and C (approx. 1:1 mixture) Compound C dominant Compounds A and D (A dominant) Compound B dominant
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- Provide the curved arrow mechanism for the reaction of the compound shown below treated with Cl2/FeCl3. Include transition states and the major product. I apprecitate the helpInterestingly, reduction of the complex shown above mostly gives thealcohol enantiomer shown below after workup. a. Draw the other minor diastereomeric alcohol product. b. Briefly explain the diastereoselectivity of the reduction – why is oneenantiomer heavily favored? Draw a structure or structures to support youranswer.Show the stepwise mechanism for the entire reaction below, including all arrows and intermediates. Your EAS should show at least one resonance form for the sigma complex.
- Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .What is the structure/s of the major organic product/s for the reaction below?Provide the answer if the compounds will react. 1. Which compound/s will react with Br2 in water under light conditions? (explain each compound; answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (explain each compound; answers may be one or more)
- (Give clear handwritten solution) give reaction mechanism and major product for the all three subparts (a,b and c) solution.Arrange the alkyl halides in order of increasing reactivity in an SN2 reaction with KI in acetone (least first). I, IV, III, II II, III, I, IV IV, I, III, II III, II, IV, IFor each reaction shown, determine which substitution mechanism (SN1 or SN2) is likeliest to predominate, and provide two reasons to support your answer.