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- 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 149Draw the alkyl bromide and the nucleophilePredict the starting alkyl bromide that would produce the product shown in the SN1 reaction. Assume no rearrangements. Stereochemistry is not considered. Draw Alkyl Bromide Reactant CH3OH
- The Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the alkane. The first steps of the mechanism convert a carbonyl to a hydrazone in a manner similar to imine formation. Draw the mechanism arrows for the reaction from the hydrazone to the alkane. Be sure to add lone pairs of electrons and nonzero formal charges to all species.A single alkyl bromide reactant theoretically yields either of the given products, depending on the reaction conditions. Draw the structure of the alkyl bromide compound.All I need help with, is everything about this process, please send help!
- Complete the following nucleophilic substitution reactions. In each reaction, show all electron pairs on both the nucleophile and the leaving group.In the following electrophilic aromatic substitution reaction, the major product results in the substitution occurring at the 2 position. Starting from each potential carbocation intermediate shown, (a) draw the possible resonance structures and (b) explain why the major product is favored. Br 4 Br2 5 Br major product minor product + Br Br 2. LOClassify the following reaction as an Sn1, Sn2, E1, E1cB, E2 reaction. Can you show me the leaving group and explain how to find a leaving group? And how to identify the other reactions?
- Draw the major and minor neutral organic products that would form when the alkene below undergoes acid-catalyzed hydration. ignore the stereochemistry, so your two products should be regioisomers.Draw curved arrows to show the movement of electrons in this step of the mechanism.Complete the following nucleophilic substitution reactions. In each reaction, show all electron pairs on both the nucleophile and the leaving group.