Predict the reagent(s) needed to produce this regiochemistry in this elimination reaction. my OH Q A B C D CH3OH CH3OH heat (CH3)3COK heat H3O+ heat =1 E ↓- H3O+
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Q18. 30 minutes left please help!!
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- Consider the following mechanism of reaction: CH3 CH, CH3 CH;C CH, + H-CI CH;CCH, + C: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic HCl and CI" are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI" are both electrophilic The alkene and CI" are both nucleophilic AMeving to another question will save this responseProvide reagents and reaction conditions for each stepGive the product of the following reaction. H₂SO4 H₂O -OH -OSO₂H ? O There is no reaction under these conditions or the correct product is not listed.
- Please answer the following questions in detail (show all the steps)What is the relationship between the products formed in the SN1 reaction below? Options: Structural isomers Enantiomers Diastereomers Identicaldraw and explain the mechanism of this reaction OH CH₂ PhCOCI in py CH3 KOH in py 3 C OH H₂SO, in 0000 CH, CON
- Draw the structure of the major organic product of the reaction below. ● + CHCI3 MILL KOH Use the wedge/hash bond tools to indicate stereochemistry where it exists. Show stereochemistry in a meso compound. If the reaction produces a racemic mixture, just draw one stereoisomer. ▼ n [F ? ChemDoodleⓇConsider the following reaction. CH3CH₂CH=CHCOH HCI CH3CH₂CH CHCOH c₁ CH3CH₂CH- H O CHCOH H CI this product is not observed Account for the fact that this reaction yields only a single product by drawing the carbocation intermediate leading to the observed product.Complete 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