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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?Sodium borohydride (NaBH4) can be used to reduce cyclohexanone to cyclohexanol. How could one us IR to determine if all the starting material has been consumed?Predict the major products formed when 2- methyl-1-butene reacts with: H2, Pt/25°C. Show the reaction mechanism the given alkene reactions
- In light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:Does the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? YES OR NOW AND WHY The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane product was trans-1,2-dibromo-1,2-diphenylethaneAcetylene is a very weak acid; however, it will react with moist silver(I) oxide and form water and a compound composed of silver and carbon. Addition of a solution of HCl to a 0.2352-g sample of the compound of silver and carbon produced acetylene and 0.2822 g of AgCl. (a) What is the empirical formula of the compound of silver and carbon? (b) The production of acetylene on addition of HCl to the compound of silver and carbon suggests that the carbon is present as the acetylide ion, C22-. Write the formula of the compound showing the acetyl ide ion.
- Acid-catalyzed hydrolysis of a nitrile to give a carboxylic acid occurs by initial protonation of the nitrogen atom, followed by nucleophilic addition of water. Review the mechanism of base-catalyzed nitrile hydrolysis in Section 20-7 and then predict the products for each reaction below and write all of the steps involved in the acid-catalyzed reaction, using curved arrows to represent electron flow in each step.20- 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?We react 2-propanone with 1º NaCN, H+, 2º LiAlH4 and 3º H3O+. Indicate the final product. Comment reactions.
- When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.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.Chemistry Give the products of the reaction of 1 mole of 2-methy1-1,3-pentadiene with 1 mole of HBr. Whichproduct(s) will predominate if the reaction is under kinetic control? Which products) will predominateif the reaction is under thermodynamic control?
