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- Draw the reaction equation of 1-bromobutane reacting with 18 wt. % sodium iodide in acetone.Remember that a reaction equation illustrates the conversion of starting materials into products) and includes a reaction arrow, specitying the conditions for the process. (b) Additionally, indicate whether this reaction follows an Su1 or Sp? mechanism.A full arrow pushung mechanism for the reactions and show their intermediatesFor the dehydrohalogenation (E2) reaction shown, draw the major organic product, including stereochemistry. Select Draw Rings More Erase H CI (CH3);COK (CH3);COH H
- Question 5. (20 points) Consider the following reaction. + PhLi (2 eq.) then water a) Propose a structure for the final product. b) Give a complete mechanism for the transformation. c) Draw an energy diagram of the transformation and briefly comment on the relative energies of the starting material, final product, and any intermediate(s), and about the rate determining step.4. The given mechanism tracks the transformation of a primary hydroxyl FG into an aldehyde carbonyl using the Swern oxidation ([0]) conditions. Examine the details of the mechanism, paying close attention to the lack of lone pairs, and then respond to the following questions. Note that "reaction arrow" refers to the arrows that separate the reaction steps. (a) Draw a box around the pE2 step (reaction arrow) of the mechanism. (b) Draw a star on any addition (Ad) step (reaction arrow) of the mechanism. (c) Draw a circle around any elimination (E) step (reaction arrow) of the mechanism. (d) When the Swern conditions are characterized as NOT over-oxidizing primary hydroxyl FGs into carboxyl FGs, to what step in the mechanism does this refer? (e) What is the leaving group for the pE2 step in this mechanism? What criteria is used to judge what makes this FG a good leaving group? H3C S=0 H3C H3C → OS- H3C CO2 CO CIO CH2 H3C H3C CH3 H3C H3C H3C CH3 H. H3C O CH3 H3C H NET3 H3C H3C H3C R R NET3For the reaction in part "b", please explain which products are the major and minor products. Also explain which are the kinetic and thermodynamic products.
- For each of the following, write the major product(s) and then draw out each step in the mechanism using curved arrows. Show ALL lone pair electrons and formal charges. Redraw ALL molecules as to show explicitly ALL bonds being broken or formed. Identify the molecular orbital (HOMO) of the nucleophile and the molecular orbital (LUMO) of electrophile involved in the nucleophilic attack. MO diagrams are not necessary..3) Show a complete mechanism and predict the product for the reaction shown below. Br₂ / H₂O Please provide perspective diagrams (wedge/dash notation), resonance forms, curved arrows, formal charges, and lone pairs as need for all species involved. With reference to the intermediate(s) involved, comment on both the regiochemistry and the stereochemistry of the process.octane + NOx + hv (assume hydrogen on second carbon bonded the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).
- ochem help please Predict the major product(s) for the following reaction sequences and provide the stepwise mechanism for both steps 1 and 2 .... (see attached image)For the reaction below, give the major produc excess Cl₂ ..) and show the complete stepwise mechanismAnswer the following questions based on the compounds below: (pictures) a) Which compound has the lower boiling point? Explain. b) Draw the SN1 mechanism for the reaction of compound B with sodiumhydroxide, NaOH.