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predict the major product of the following reaction and then draw a curved arrow mechanism for its formation,.
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- 4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3When phosgene is treated with excess methanol, a product is formed whose "H NMR spectrum shows one peak-a singlet at 3.8 ppm. Provide a complete, CH,OH ? CI CI detailed mechanism for this reaction. PhosgeneQ.11
- Payalbena,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.On a scrap piece of paper, draw a curved arrow mechanism for the following reaction. Once you have determined the major product, draw it in the space provided below. م سيد NH₂ CH₂O, HCl(cat.)
- 4) Provide a synthesis of the following compounds using the given starting material and any other reagents. starting material final product CI starting material final product OH OH OH starting material final product 5) Provide an arrow-pushing mechanism for the following reaction to get to the product shown. HON OH H₂O*, H₂O НО مله1) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors (structures), the regiochemistry that results in each case. OMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3Draw a detailed mechanism for the following reaction and include the major product
- Draw a step-wise mechanism for the following substitution reaction. Be sure to add lone pairs and charges where relevant. CI H₂OC Show the complete mechanism and the product formed. AlCl3 ?On a scrap piece of paper, draw the curved arrow mechanism for the following reaction. Once you have determined the major product, draw it in the space below. 1) Ph MgCl, Et₂O 2) NH,C, H,O