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- Draw an energy diagram for the following SN2 reaction. Label the axes, the starting materials, and the product. Draw the structure of the transition state.The reaction of methylpropene with HBr in ether gives one of the two products below as the major product. Br HBr Br ether Product A Product B Product would have a higher energy transition state for the formation of the intermediate leading to it. O A O B O Both products would have the same transition state.Q11
- 22. Draw all the alkene products that can be prepared in the following E2 reaction. Circle the alkene that you expect to be the major product based on Zaitsev's Rule. Use curved arrows to show how the major product forms. ما "OC(CH) analghaq my2A 16nsiqi UnA 2 ebileria lenims ocation intermediate affect the rate of an El reaction? mainsroom 13 no 101 ws! sbubal .mainsrbM 13 phen Snobia to mzinaroam bevlovni el sisibamish 149Which SN2 reaction will occur most rapidly? (Assume the concentrations and temperatures are all the same.) * CH;0 + ^CI CH3 + CI- CH, B CH,0 + CH + F CH,O + CH, CH,O Br Br DSN1 reactions undergo carbocation rearrangements, but E1 reactions do not because the carbocation intermediate does not last as long during the elimination process. True O False
- Which of the compounds shown below can undergo an SN2 reaction? A OTS Br 1) Compound C 2) Compounds B and D 3) Compounds A, B and D 4) Compounds A and B B C Br Br DDraw the missing reactants/ intermediates in this SN1 mechanism. Include all lone pairs. Ignore byproducts.Ignore stereochemistry. I dissociation I Select to I Draw I I Carbocation Intermediate I Carbocation Rearrangem ent Select to Draw Carbocation Intermediate & NaBr I I I I I I IDoes the following SNAr reaction occur accordingto an addition-elimination or an elimination-addition mechanism? Motivate.
