QUESTION 10 [12] Propose mechanisms for the following reactions. нуло до (a) NH2 H. O (b) Ph-C-CI (c) Ph-C-OCH3 (CH3)2CHOH NaOH H₂O Ph-i-oc Ph-C-OCH(CH3)2 Ph-8-8 Ph-C-+ CH3OH
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- Please help with the following... Draw the bond line structured for the reactants and the products obtained in the following reactions: 1. m-tertbutyl benzoic acid + 3-methyl-1butene, HF 2. 3-chloro-2,6-dinitrotulene + sodium ethoxide, ethanol 3. o-methylanisole + isobutanol, BF3I’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 the presence of acid such as H2SO4, 3,4-dimethyl-1-pentene undergoes isomerization to 2,3-dimethyl-2-pentene (shown below). Write a complete mechanism, showing all steps and using curved arrows to explain this observation.
- Predict and draw the structural formal of the product(s) of each of the reactions below. Butanone+H2 -------> PtExplain and detail the reaction mechanism: NaBr + H2O + n-butyl alcohol = ?OCHEM... Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with methanol. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also, indicated which step is likely to be rate-determining.
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