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Predict the products of the following elimination reaction and indicate which is the major product
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- I’m currently trying to write a lab report for the synthesis of dimolybdenum tetraacetate [Mo2(O2CCH3)4] from the reaction of molybdenum hexacarbonyl, Mo(CO)6 in glacial acetic acid and acetic anhydride under a nitrogen atmosphere, involving the difficult formation of a quadruple bond and requires high heat and long reaction time (approximately 20 hours). But these are the question I’m stumped on: 1. Why need the reaction be done under nitrogen? We also added dichlorobenzene and hexanes during the reaction. 2. Explain the purpose of dichlorobenzene and hexanes. 3. Why does the reaction take 20 hrs?In light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:(ii) The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products. Draw a mechanism for the reaction which produces the major organic elimination product and provide a rationale as to why that is the major product.
- Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)22- Give one example for the hydration of Alkene: That is the Addition of H2O byoxymercuration. Give the proper Mechanism if possible.23- Give one example for the hydration of Alkenes: that is: the addition of H2O byHydroboration.1. Write equations, using displayed formulae, to show the conversion of but-1-eneinto:a) polybut-1-eneb) 1,2-dibromobutane 2. a) Explain why alkenes tend to react with electrophiles.b) Show the mechanisms for the following reactions:i) ethene with bromineii) but-2-ene with hydrogen bromidec) Explain how bromine can behave as an electrophile. 3. Reaction of but-1-ene with HBr gives two products in unequal amounts. In eachcase, identify the two products, state which is the major product, explain why it isthe major product and give the mechanism for its formation.
- Fill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.(ii) The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products. Draw a mechanism for the reaction which produces the major organic elimination product and provide a rationale as to why that is the major product.(with explanation)The following halide reacts differently with hydrogen sulfide as shownshown in the attached image reactions. For each reaction, show the mechanism, draw the energy diagrams for the formation of each product and write the rate equation for the formation of each product. PD: mechanisms are SN1,SN2,E1 etc
- The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?Pls solve this question correctly in 5 min i will give u like for sure Balance the chemical equation of a reaction formed by the bromination of trans-cinnamic acid if we started with 0.3088 grams of trans cinnamic acid and 1mL of bromine. The product of this reaction is 2,3 - dibromo - 3- phenylpropanoic acid20- Show and write the correct reactions of the addition of 2 moles of HBr to 1-Hexyne.21- Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-Butene?