1) Assign the aromatic signals for both 4-tert-butylphenol and the specific product you formed. g Br2 Br- a OR HO HO HO `Br 2) Explain how you could use NMR to determine what regioisomer formed in this reaction. 3) Draw resonance structures of 4-tert-butylphenol that show which aromatic carbons have high electron density and explain why you obtained your product in this experiment.

1) Assign the aromatic signals for both 4-tert-butylphenol and the specific product you formed. g Br2 Br- a OR HO HO HO `Br 2) Explain how you could use NMR to determine what regioisomer formed in this reaction. 3) Draw resonance structures of 4-tert-butylphenol that show which aromatic carbons have high electron density and explain why you obtained your product in this experiment.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 54AP: The 1HNMR spectrum shown is that of 3-methyl-3-buten-1-ol. Assign all the observed resonance peaks...

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