One of these molecules reacts faster via an E2 reaction. Draw the products from each E2 reaction. Draw one or more chair conformations to clearly demonstrate why one product forms from this reaction. Br: tBuOK A 8 Br tBuOK
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- One of these molecules reacts faster via an E2 reaction. Draw the products from each E2 reaction. Draw one or more chair conformations to clearly demonstrate why one product forms from this reaction. :Br: od HOaM malandboM :Br:1. Using Newman Projections, show how each product can be produced through a periplanar transition state in the following E2 reaction. NaOEtPlease explain the steps from the reactant to product. Are they SN1/SN2/E1 or E2 reactions, good or bad leaving groups.
- SN1 reactions undergo carbocation rearrangements, but E1 reactions do not because the carbocation intermediate does not last as long during the elimination process. True O FalseDraw the final major product(s) for each multistep reaction. MeCI NBS NaOH РСС AICI3 light CH2CI2Consider 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.
- 6. Draw a mechanism for the following Sn2 reaction. H2O OH ye y앤 + H3O+Consider the elimination reaction shown here, which CH3 H3C Base produces a mixture of diastereomers. Based on the stereochemistry of this reaction alone, is it possible to tell whether the reaction takes place via an E1 or an E2 reaction? Explain. H H3C Br H3C CH3 CH36) One of the alkyl halides undergoes E2 elimination much faster than its diastereomer. Why is there a difference in their reaction rates? CI ak * NaOMe (E2 rxn is slow) NaOMe CI (E2 rxn is fast) Only one product formed Two products formed