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- NH 1) xs Mel 2) Ag2O, H2O, A 2. Complete the following reaction. Show the intermediate, and propose a mechanism for the second step.Draw a mechanism for the reaction below. SHOW ALL BOND-FORMING AND BOND- BREAKING STEPS. SHOW ALL INTERMEDIATES. Но. [H*] HOProvide a complete mechanism for the reaction, including all lone pairs, formal charges, and curved arrows. CI O OH
- OH OH ∞∞ BF3 Et₂O This reaction takes place via a pinacol rerrangement. Please, draw curved arrows to show the movement of electrons in this SPECIFIC step of the reaction mechanism. +BF3 HO: :OH OH (BF3OH)5) Fill in the missing reagents for the total synthesis below. For the final step, propose a mechanism for the transformation. NC MeO₂C OMe OMe OMe OMe Me Me OHC Me MeO2C Me Me Me Me Me Me .OH Me -x-x-- Me HO₂C MeO2C OMe BBr3 Me Me Me Me Me Me H Me Me Me CH₂OH Me H OH CH₂OTS Me H MOH CH₂OTS Me H --- Me H Me Me Me H Me Me Me H Me "Me Me H Me H NH2 Me H * - * - Ø H Me Me Me H Me Me Me H Me Me Me Me H H Me Me Me HComplete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3
- Instructions: a,ß-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Use this information to answer the following question(s). + Nu-H Nu H Refer to instructions. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.Draw the simplest mechanism possible for the reaction below. You may need to re-draw structures to show bond lines or lone pairs. 0 Ö S он, H₂N-C- + H C-H H ОН Н H₂N-C-C-H H H + + H olo ArOH CH3OH HⓇ OCH 3 In the space provided below please show a detailed, stepwise mechanism for the transformation shown above. You must show all intermediates (including proton transfer