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Which compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)
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- 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 eliminationWhy is this E2 reaction wrong?How do you identify if a reaction is Sn1 Sn2 E1 or E2? Draw a flowchart to identify if reactions are SN1 SN2 E1 or E2.
- Consider the following E2 reaction.a.Draw the by-products of the reaction and use curved arrows to show the movement of electrons. b.What happens to the reaction rate with each of the following changes? [1] The solvent is changed to DMF. [2] The concentration of −OC(CH3)3 is decreased. [3] The base is changed to −OH. [4] The halide is changed to CH3CH2CH2CH2CH(Br)CH3. [5] The leaving group is changed to I−.Identify the correct transition state for an E2 reaction.Make a table with the main conditions for each mechanism: E1, E2, SN1, SN2.
- Draw the structure (including stereochemistry) of an alkyl chloride that forms each alkene as the exclusive E2 elimination product.Which compound would undergo carbocation rearrangement during an SN1 reaction? A B C DThe molecule, 2-bromo-1,3-diethyl-1,4-dimethylcyclohexane undergoes an SN1/E1 reaction in the solvent ethanol. i) Draw the intermediate resulting from the first step of this reaction. ii) Draw the two most favorable intermediates resulting from carbonation iii) From the intermediate(s) in (ii) draw all the possible E1 products and circle the product(s) that is(are) most favorable. iv) Name the most favorable product(s). v) Draw an SN1 product from an intermediate in (ii).