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Part III - Mechanism (14 marks] A. Use the curved arrow notation to draw the step-wise...
Please explain with mechanism I'm so confused what mechanism I should have to use. Part III - Mechanism (14 marks] A. Use the curved arrow notation to draw the step-wise reaction mechanisms that account for the formation of the products shown in the transformation below. All reactants are shown. (8 MARKS] MeOH осна + -TsOH
A. Use the curved arrow notation to draw the step-wise reaction mechanisms that account for the formation of the products shown in the transformation below. All reactants are shown. (8 MARKS] OES=0 MeOH w осн. -TsOH
A. Products and Mechanism 1. Draw a detailed step-wise mechanism using curved arrow notation for the following reaction: EtO E t 1. xs PhMgBr 2. HCI, H,0
Part III - Mechanism cont'd B. Using curved arrow notation, draw the reaction mechanism and predict the product the reaction below. Show all reaction intermediates and account for stereochemical requirements. [6 MARKS] or EtoNa / EtOH ? OTS Heat
16. [10 pts) Use curved-arrow notation to write out a detailed, step-wise mechanism for the following transformation. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. (If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken!)
5. [5 pts] Use curved-arrow notation to write out a detailed, step-wise mechanism for the reaction listed below. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken! HBr r Mechanism: +4 +
Draw the curved arrow notation for each elementary step of the mechanism described below. In each step, be sure to include all relevant electron pairs, reactants, and products. NOTE: you are showing a mechanlsm. Therefore, the product from elementary step 1 is the starting materlal for 2, the product from 2 is the starting material for 3, and so on. 2. 1) proton transfer involving HCI 2) heterolysis OH 3) carbocation rearrangement 4) electrophilic addition involving benzene (CgHg) 5) electrophilic.elimination
I need some help with part b in the question please (a) Propose a one-step mechanism using curved arrow notation for the formation of styrene oxide from styrene using MCPBA, as shown below. (b) Propose a step-wise mechanism using curved arrow notation for reaction of styrene oxide with (CH_3)_2 CHNH_2 that includes the structure of the expected product. To simplify the mechanism, do not show formation of enantiomers.
4 4) Write the reaction product and use the curved arrow notation to draw a mechanism that accounts for the formation of product upon oxymercuration/ reduction of cis-4-hexenoic acid in aqueous THF. (8 points) a) Write the reaction. 1) Hg(OAC), aq, THE 2) NaBH, aq. THE HO cis-4-hextenoic acid b) Write a mechanism.
B. Using curved arrow notation, draw the reaction mechanism and predict the product the reaction below. Show all reaction intermediates and account for stereochemical requirements. [6 MARKS) EtOna / EtOH ? OTS Heat