Classify each of the following organic reactions. Check all that apply for each organic reaction. Classify each of the following organic reactions.reactionHBr1) Hg(OAc)2, H₂O2) NaBH4Cl₂BrCIx = x²Cl₂H₂OCIOHCIOHtype of reaction(check all that apply)dihydroxylationenolationhalogenationhydrogenationhalohydrin formationadditionformation chelationhalogenationadditiondihydroxylationOhalohydrin formationhydrogenationhalohydrin formationdihydroxylationadditionhydrogenationoxyhydrationhalogenationhalohydrin formationdihydroxylationhalogenationdihydrinationhydrogenationaddition×

1st ReactionReaction Type: This is an electrophilic addition reaction where HBr adds across the…

Answered: Classify each of the following organic…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 28VC

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Classify each of the following organic reactions. reaction Hör H₂O 1) Hg(OAc)₂, H₂O aveau Br OH OH type of reaction (check all that apply) Odihydroxylation addition hydrogenation Dhalogenation halohydrin formation. subtraction halogenation hydrogenation addition halohydrin formation inhalation Odihydroxylation addition hydrogenation oxyhydration halogenation
Complete the following reaction of hydrolysis using arrows and drawing the intermediate products Catión estabilizado por resonancia Catión oxonio MeO OMe - MeOH R R Acetal Catión oxonio Catión oxonio Meo OH R- R Hemiacetal MeOH Catión estabilizado por resonancia -H® R R Compuesto carbonilico
Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
The following reactivity order has been found for the saponification of alkyl acetates by aqueous NaOH. Explain. CH3CO2CH3 > CH3CO2CH2CH3 > CH3CO2CH(CH3)2 > CH3CO2C(CH3)3
When cis-2-decalone is dissolved in ether containing a trace of HCl, an equilibrium is established with trans-2-decalone. The latter ketone predominates in the equilibrium mixture. Propose a mechanism for this isomerization and account for the fact that the trans isomer predominates at equilibrium.
Which is the major product from the acid catalyzed hydrolysis of cyclohexene oxide? но OH но он || II IV
Through the use of a mechanism, identify the intermediate and the product of this reaction. Explain any selectivity involved and the origin of such. 요요 i) NaOEt/EtOH H3O+ K C21H2003 LC18H160 Ph Ph OEt ii) H3O+ heat
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Some elimination reactions can undergo cation rearrangements. Given the following reaction conditions, draw three possible elimination products that could form with carbocation rearrangement, or without carbocation rearrangment. Include major and minor products. Br Weak Base
Which of the following undergo decarboxylation upon heating? CO,H OH CO,H CO₂H & & & IV CO,H CO₂H II III CO₂H V CO,H
Can you help identify the missing reagents and products and identify the type of reaction?
i

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