(5pts) Provide the complete arrow pushing mechanism for the chemical transformationdepicted belowUse proper curved arrow notation that explicitly illustrates all bonds being broken, andall bonds formed in the transformation.Also, be sure to include all lone pairs and formal charges on all atoms involved in theflow of electrons.CH3OHI ICH3O-HHI ①H

Detailed Explanation for the given chemical transformation: Nucleophilic Attack The reaction begins…

Answered: (5pts) Provide the complete arrow…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.21P

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3. The reaction in this experiment contains iron nitrate and potassium thiocyanate as reactants, and iron thiocyanate and potassium nitrate as products. Please draw the Lewis structure for thiocyanate and nitrate. Be sure to show non-zero formal charges. ded to a tathyl violet solutical Dmlain n temof Eplain hed methy violer solt of of Le c sining solid to A solution contain and Terms of Le Chatellsprincple 87
99,00%6 ملا ت مها احمد (A A) B) ma not بوك هلا حد ده A6 99.9999% Br a.) Given our discussions of this mechanism express in a reaction coordinate diagram the two reactions above. * Please exaggerate scale for clarity* +HBr
Solve a and b with detailed explanation
3) Enols are an important class of molecules in organic chemistry, which are utilized for theirability to form carbon-carbon bonds. We will learn about their unique reactivity much later inthe course. Shown below is an enol on the left, whereas the molecule on the right is classifiedas an allylic alcohol. a) Please explain why the structure on the right IS NOT a resonance structure of the enol on theleft. A short statement or illustration is fine, be sure that your rationale is clear. b) Draw the correct resonance structure that can be produced from the enol on the left. Besure to include arrows to indicate the movement of electrons in the left-hand structure andindicate charges in the resulting structure. c) What is the hybridization of the carbon indicated with the red arrow?
6. In an organic chemistry lab, chemists were attempting to convert compound I into compound III via a substitution reaction To their surprise, compound II was the only observed compound after treating compound I with cyanide. "CN observed not observed a. Provide a detailed, stepwise mechaniem for the transformation above that accounts for the formation of product II. Use the curved arrow formalism to show the flow of electrons. Show all lone pairs, intemediates, formal charges, and pertinent resonance structures. b. Explain why product II is formed instead of product III. Use dawings to supportyow answer. C Would you expect compound II to be optically active? Briefly explain. Note The reaction above was run on an enantiomerically pure sample of compound I. CN.
3. An alkene can be converted into an ether in the three mechanistic steps shown below. Complete this mechanism by: Draw curved arrows to indicate the flow of electrons for each step. Lone pairs are omitted for clarity but be sure to include lone pairs on atoms that are involved in bond formation/breaking. Draw the reaction intermediates in the appropriate boxes. Include all nonzero formal charges. Classify each step of the mechanism using the boxes below each arrow as one of the following: acid- base proton transfer (AB), nucleophilic attack (NA), elimination (E), or rearrangement (R). + H-OMe H-OO + MeOH + MeOH + H-OMe H-OO 48
Please don't provide handwritten solution ...
Rewrite the entire reaction in Full Structure Format with the Ending Products [The second image is an example of Full Structure Format ] THANKSSSSSSSSSSSS
Provide a complete curved arrow mechanism that accounts for the transformation below. Be sure to show all arrows, reation intermediates, lone pairs, and formal charges
Rationalize the formation of compound B using the arrow-pushing formalism. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H: EXP CONT Submit Request Answer Br: H UN Br 6:46 PM
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