a) Is this reaction SN1/E1 or SN2/E2 ? b) For the reaction draw a mechanism for the formation of substitution product and elimination product. c) What is the rate law for the substitution reaction? d) Draw the energy profile diagram for the substitution reaction? e) What is the appropriate solvent for the reaction? protic or aprotic solvent.Explain why that appropriate solvent is good for the above reaction?
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- a.) What is the mechanism of the reaction? b.) What is the mechanism when HCl is added to the product?Question: Draw the mechanism of the reaction you will complete in lab. Use the proper arrow drawingconvention to show all bond making and bond breaking steps in the reaction. Background info: A substitution reaction takes place when a nucleophile (Nu:) forms a bond with a carbonatom, displacing a leaving group (L).SN2 reactionLeaving groups are typically weak Bronsted bases that are stable as anions (often halide anions).The precise timing of when the leaving group leaves depends on the structure of the substrate –the molecule bearing the leaving group. Methyl and primary alkyl halides tend to undergo SN2type reactions. In this type of reaction, the nucleophile attacks the carbon from the side oppositethe leaving group and the nucleophile-carbon bond is made simultaneous with the carbon-leavinggroup bond breaking. SN2 reactions are one-step and there is an inversion of stereochemistry atthe carbon bonded to the nucleophile.SN1 reactionIf the carbon undergoing substitution is…An appropriate mechanism for the following reaction.
- Draw generic mechanism for SN2 & SN1 reactions.How is the rate of the reaction affected when concentrations of both nucleophile and alkyl halide are doubled for SN' reaction? (A) rate is doubled B) rate remains the same c) rate is tripled D rate is quadrupled(4 times)Mechanism... Please show all steps including Curved arrow to show flow of electrons and all reagents present.
- Place the appropriate solvent (DMSO or HOCH3) under the reaction arrow for each of the following substitution reactions substitution reactions, so that they proceed in the forward direction. Explain your choice at the right. 6. .CI Nal Solvent? NaCI Solvent?The substitution reaction studied here with Chlorobutane and KOH is known to have a second order rate equation meaning the transition state in the slow step involves both nucleophile and electrophile. Knowing that, which of the following statements are true? Select all that apply. A) Adding more Chlorobutane (the electrophile) will not change the rate of the reaction. B Adding more KOH (the nucleophile) will make the reaction go faster. Adding more Chlorobutane (the electrophile) will make the reaction go faster. D) Adding more KOH (the nucleophile) will not change the rate of the reaction. E Adding more KOH (the nucleophile) will make the reaction go slower.In the given synthetic transformation, which basic reaction type best describes the two reactions? (The number in the answer corresponds to the number of reactions) 1. H2SO4, H2O 2. CrO3, py Step 1: choose your answer... Step 2: choose your answer... choose your answer... Substitution Next Proton transfer Addition Elimination Oxidation