Are the statements (I-III) true descriptions of the reaction shown? Use the dropdown menu to give your answers. BH3, THF I The reaction does not involve rearrangement IL The reaction is stereospecific III The boron atom acts as a nucleophile I: choose your answer... II: choose your answer... II: choose your answer...
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- Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?Please help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.this is not graded quesiton; the reactions are all covered in Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise. Chapter 15-17; why is this violating the term of use??? i dont't understand. this is not a graded quesiton
- quesition 1; image questions 2; What type of reaction is this?Choose one: bimolecular /homolytic /substitution/initiation/coupling/SN2/addition2A---> 2B + C (Kp1) 2D---> 2E + C (Kp2) Now find the corresponding Kp3= f(Kp1, Kp2) = ?for this reaction: D + B----> A + E elaborate throughly with every step and annotationThe electrophilic addition reaction shown below involves a carbocation rearrangement. For the mechanism step below, draw curved arrows to show electron reorganization. Use the arrow tool to specify the origin and the destination of the reorganizing electrons. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond. I understand how it's supposed to be laid out. I'm just unsure of where the first arrow comes from as there are a lot of positions. I have attached examples on what positions I mean. Thank you.
- help me please. all the reactions shall be covered in Chapter 12-15 from Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise. please make sure your answer fits the question; thank you! I posted the same question before and someone gave same answers to all of the questions :(organic chemistry 1 Provide an overall order of carbocation stability, including every type of carbocations. (Not just primary< secondary<tertiary!) please help me this question, thank you!help me please. all the reactions shall be covered in Chapter 12-15 from Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise.
- Please complete reactions in clear handwritten of all subpartsPredict the major organic product formed when the compund shown below undergoes a reaction with H2O2 and then is heated in H2O. The 2nd photo is what I thought was the answer, but when I put it into Mastering Chemistry, it was counted as wrong and my feedback was, "What configuration is the C=C bond expected to haev?" I'm confused as to what this is referring to, so I appreciate any help given.Finding/figuring out what is a major product is something I struggle with, please send the help for understanding every step of what this reaction should be with the major products for my complete understanding!