Provide the complete mechanism using Curved Arrow Formalism to show the reaction of p-t-butylaniline treated sequentially with i) acetic anhydride; ii) HNO3 @20 degrees C. ) Provide the 1H NMR data for the product generated above in Question #10. Redraw the compound here and clearly label which 1H is being reported. You must report the data in the format of chemical shift, integration, multiplicity (eg 8 1.0, 3H, triplet). Tell how many signals would be visualized in the 13C NMR spectrum for the compound.

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Provide the complete mechanism using Curved Arrow Formalism to show the
reaction of p-t-butylaniline treated sequentially with i) acetic anhydride; ii) HNO3 @20
degrees C.
Provide the 1H NMR data for the product generated above in Question #10. Redraw
the compound here and clearly label which 1H is being reported. You must report the data
in the format of chemical shift, integration, multiplicity (eg 8 1.0, 3H, triplet). Tell how
many signals would be visualized in the 13C NMR spectrum for the compound.
Transcribed Image Text:Provide the complete mechanism using Curved Arrow Formalism to show the reaction of p-t-butylaniline treated sequentially with i) acetic anhydride; ii) HNO3 @20 degrees C. Provide the 1H NMR data for the product generated above in Question #10. Redraw the compound here and clearly label which 1H is being reported. You must report the data in the format of chemical shift, integration, multiplicity (eg 8 1.0, 3H, triplet). Tell how many signals would be visualized in the 13C NMR spectrum for the compound.
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