Part 2. Predict the Organic Products. Predict the major organic product(s) for each of the following reactions. Be sure to show stereochemistry when appropriate. 1) BH3/THF 2) H₂O₂/NaOH/H₂O
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- 1. Write organic products of the following reactions. Show stereochemistry where appropriate. Br₂ H₂O H₂O H₂SO4 1. BH3: THF 2. H₂O2, NaOHAlcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.Chemical Reactions. Give the structure of the major organic products formed in each of the following reactions Br Br CH₂ONa CH₂OH t-BuOK DMSO +H₂N- 《》-NH,
- Part 2. Predict the Organic Products. Predict the major organic product(s) for each of the following reactions. Be sure to show stereochemistry when appropriate. α 1) 03 2) (CH3)2SThis is a multistep syntheses. More than one reagent/reaction will be necessary to produce the product. Provide all necessary reaction conditions (HBr, HgSO4, etc.) and the products produced after each step of the synthesis.Provide the principle organic product for the following reactions. If more than one product is formed indicate which one you expect to be the major product.
- 3) A common practice that organic chemists work on is a process known as retrosynthesis. In this a chemist will take known reactants and devise a synthetic pathway to produce the desired products using reactions that they know. As you proceed through organic chemistry you will be tasked with thinking about this process. How would you make the desired final product starting from the alkyne. It will take a couple of reactions. Please show the reagents necessary. And for your last step please show the arrow pushing. Starting material Br Product Br ...Provide the major organic product of the following reaction. + { A1C13CH3 གོན་ནི། ཡོན་ Br₂, H₂C CH₂Br H3C CH3 H₂C CH3 Aldehydes and ketones can be halogenated at their a-position by reaction with Cl₂, Br2, or 12, under acidic conditions. Using Br₂ under acidic conditions, an intermediate enol is formed which adds bromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less favorable. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :0: :OH н-он H-OH₂ H₂O H₂C. H3C. CH3 CH3 H3C CH3 H3C CH3 Σα
- Predict the major product for this reaction. Ignore inorganic byproducts. 1. dicyclohexylborane 2. H2O2, NaOHPart 2. Predict the Organic Products. Predict the major organic product(s) for each of the following reactions. Be sure to show stereochemistry when appropriate. Mil m-CPBA CH₂Cl2SCHAU Instructions: Use a separate sheet of paper when necessary 1. Draw structures, including all necessary conditions for the following reactions: Organic Reactions Part 2 a) the production of cyclobutyl benzoate from its starting compounds. b) the dehydration of 3-bromohexan-1-ol. c) the condensation of 3-pentanoic acid and N-ethylethanamine. 2. Starting with butene, show how you could prepare butanoic acid in three reaction steps. 3. Write a reaction that shows the production of isopropylbenzene (cumene) from benzene and the appropriate isopropyl derivative. 4. Propose a 2-step mechanism to produce the following compound from the appropriate alcohol. d. Alcohol b. What difficulty would you expect to encounter during this synthesis? 5. Complete the following reactions by filling in the blanks with appropriate structures and/or conditions. H₂O H₂C- NHẠCH, OH malom H₂C H₂O