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Q: Draw the Zaitsev product formed when 2,3‑dimethylpentan‑3‑ol undergoes an E1 dehydration.
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Q: 6. Identify the reagents in the following reaction scheme: OH Br -CH3 CH3 CH3 CH3 CH3
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Q: 3. Indicate the reagent that would accomplish each of the following reaction: СООН ċ-0-C-CH3
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Q: H3C CH3 KMNO4 CH3
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- Acetal product formation is difficult, since hemiacetals are stable while acetals are not stable. True FalseWrite the step(s) needed to convert CH3CH2Br to each reagent: (a) CH3CH2Li; (b) CH3CH2MgBr; (c) (CH3CH2)2CuLi.Show a stepwise mechanism by pushing arrows and drawing all intermediates. Draw a detailed mechanism for the addition of H2O to 2-methyl-2-pentene in the presence of H2SO4.
- Provide the reagents necessary to achieve each transformation. Draw the intermediate structure(s).Illustrate Dehydration of 2° and 3° ROH—An E1 Mechanism ?Acid-catalyzed bromination of pentan-2-one (CH3COCH2CH2CH3) forms two products: BrCH2COCH2CH2CH3 (A)and CH3COCH(Br)CH2CH3 (B). Explain why the major product is B, with the Br atom on the more substituted side of the carbonyl group.
- 1,2 addition of Br2 to an alkene results in a _______________. A. alcohol B. vicinyl dihalide C. alkyl halide D. geminal dihalideDraw the major product of this reaction. Ignore inorganic byproducts. 1. LiAIH4 2. Neutralizing work-upDraw the Zaitsev product formed when 2,3‑dimethylpentan‑3‑ol undergoes an E1 dehydration.
- N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes and alkynes. Keeping this in mind, draw a stepwise mechanism for the following addition to but-2-yne.Primary and secondary alcohols can be converted to alkyl chlorides via treatment with thionyl chloride. The reaction proceeds via an SN2 mechanism with inversion of configuration at the chiral carbon.Draw curved arrows to show the movement of electrons in this step of the mechanism.The sequence for the synthesis is shown, Draw the "intermediate product" after the reaction with reagent 10.