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Q: + Nal II II IV
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Q: Predict the product for the following SN1 reaction. Nal II IV 0000
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- Can you answer it and explain it? State the mechanism in which through reaction proceeds sn2 or sn1Rank the nucleophiles in each group in order of increasing nucleophilicity. a.−OH, −NH2, H2O b.−OH, Br−, F− (polar aprotic solvent) c.H2O, −OH, CH3CO2−Which compound is more reactive in an SN1 reaction? In each case, you can assume that both alkyl halides have the same stability.
- Rank the following compounds in order of their reaction rates in an SN1 reaction with HOCH3 with 1 being the fastest reaction and 4 being the slowestWhich compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)Consider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:
- From 1 being the least reactive and 4 being the most reactive rank the following alkyk chlorides in terms of increasing reactivity via SN2 reaction mechanism.Predict and draw E2 product a) Base.For each statement below, label it as causing a faster or slower rate for an E1 reaction. If it doesn’t effect rate at all then label it as neither. Stronger base Increase base concentration Switch leaving group from Cl to I Switch leaving group from 2˚ to 3˚