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Give detailed mechanism Solution with explanation needed don't give Ai generated solution avoid handwritten Solution
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- Finish the indicated reaction by filling in and starting materials, reagents or products as needed Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. H3O+Please help me with a drawn mechanism for the reaction shown.
- Please show a drawn mechanism, including intermediates where necessary for the reaction shown below. A drawn mechanism showing arrows and the movement of charges/electrons aids in understanding more than just walls of text.Draw the structure of the major organic product of the reaction. O CH3 CI 1. LiAlH4, ether 2. H₂0* • You do not have to consider stereochemistry.2. The following carbocation is generated as an intermediate in the addition of H-Br to an alkene. Draw the structure of all possible alkenes that could have formed this intermediate.
- 2) Draw all products formed in the following SN1 reaction. Br CH;CH2OHClassify the reaction below as an oxidation, a reduction, or neither.(CH3)2CHCH2OH → (CH3)2CHCHOA) oxidationB) reductionC) neitherThe pictured reaction shows an alkyl bromide being converted into an alkene. Choose all reagents that would produce the pictured alkene as the major product. A) NaOH/H2O B) H2O C) tBuOK/tBuOH D) EtONa/EtOH
- Draw an energy diagram for the addition of hydrobromic acid to pent-1-ene. Two products formin this reaction; draw the curves for both. Label the positions of the reactions, intermediates,and products. What is the name of the product that forms from the curve that has the higher-energy carbocation intermediate? What is the name of the product that forms from the curvethat has the higher-energy first transition state?The product of both the higher-energy carbocation intermediate and higher-energy first transitionstate is 1-bromopentane.Which is true of a free energy diagram for an SN1 eaction? It shows one transition state. It always shows that the reaction is net exothermic. It never shows intermediates. It always shows that the reaction is net endothermic. It always includes multiple energy barriers.Suggest a reasonable mechanism for the reaction shown Br here. HO CH;CH,OH