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- a. Draw the structures of all the elimination products. b. The reaction occurs through an E2 mechanism. Using one of your products writethe mechanism of the reaction using curved arrows. c. Is this reaction regioselective? Explain your answer. d. Explain why the reaction is stereoselective.A nucleophilic addition is not considered SN1 or SN2 because: A.) The reaction proceeds through an E1 mechanism or E2 B.) There is no carbonyl substitution when doing the addition to this C.) The solvent for this reaction is non-aqueous D.) The solvent for this reaction is non-polar1. In both SN1 and SN2 tests, why should 2-chlorobutane react more slowly than 2-bromobutane?2. Why is benzyl chloride reactive in SN1? In SN2?3. Why is bromobenzene unreactive in both tests?
- Hydroxy aldehydes A and B readily cyclize to form hemiacetals. Draw the stereoisomers formed in this reaction from both A and B. Explain why this process gives an optically inactive product mixture from A and an optically active product mixture from B.Explain the effect of the structure of the alkyl halide on elimination through E1 and E2.Please fill out for each reaction i.Fill in the missing starting materials, products, or reagents as necessary.If no reaction occurs, write "N.R." and explain why this is the case. ii. Label each transformation as SN1, SN2, or acid/base. iii. Indicate if the product is racemic or a single enantiomer.
- E2 elimination takes place under the same conditions as SN2 substitution and the reactions compete with each other. Which of the following statements is true? a) E2 elimination and SN2 substitution proceed through the same intermediate step b) E2 elimination is only possible for compounds that react with the SN2 mechanism c) In competition, a strong base favors a substitution reaction d) Steric hindrance favors E2 eliminationWhat is the SN1 mechanism between t-Butyl bromide and ethanol?Select the member of each pair that shows the greater rate of SN2 reaction with KI in acetone.