#9). Other picture is the instructions on how the arrows must be shown. Specifying Hotspot End Position InstructionsMake the ends of your curved arrows specify the destination of the reorganizing electron(s) as exactly aspossible. Keep in mind that not all hotspots are interchangeable; for example, an arrow starting/ending at theinterior of an atom (represented by an atomic symbol) is not the same as an arrow starting/ending at a lone pair.correctH-ti:incorrectcorrectHH₂CC+incorrectHCH3H₂C-C+CH3CH3CH3-H*-H*H*H*H₂C=H₂C=CCH3CH3CH3CH3 OHH3C-ofHHO:H3C-C -H-HHOAcAcO-OAC*Dess-Martin periodinane provides means to oxidize a primary alcohol to an aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond isformed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be recovered.Draw curved arrows to show the movement of electrons in this step of the mechanism.Arrow-pushing InstructionsAOC XTACOOAcH3C-OAcH-AcoCH3H-OAcHOAC

here is given a step involved in oxidation reaction of alcohol, where -OH group of alcohol attacks…

OH TH -H H N H3C- Dess-Martin periodinane provides a means to oxidize a primary alcohol to an aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be recovered. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions HỌ: →XT OAc AcO OAC a d H3C H3C-C-H H ACO OAc -OAC ACO HO CH3 -OACH OAC

OH TH -H H N H3C- Dess-Martin periodinane provides a means to oxidize a primary alcohol to an aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be recovered. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions HỌ: →XT OAc AcO OAC a d H3C H3C-C-H H ACO OAc -OAC ACO HO CH3 -OACH OAC

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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