Imine formation is an acid-catalyzed process, however the procedure performed in this does not require the addition of an acid. Suggest a viable source of acid in the carbinolami protonation reaction depicted below. Consult Scheme 8.2 for the complete mechanism. H2N-Ph Carbinolamine (hemiaminal) H :0: H o: H Ö: H 0: H H .Ph Ph PhCH H,Ñ-Ph Ph Ph Ph Ph - H H. нн H2N-Ph non-productive side reaction H* - H H H H-O: H Ph - H20 Ph S Ph Ph Ph Ph :B H. Imine Iminium ion

Imine formation is an acid-catalyzed process, however the procedure performed in this does not require the addition of an acid. Suggest a viable source of acid in the carbinolami protonation reaction depicted below. Consult Scheme 8.2 for the complete mechanism. H2N-Ph Carbinolamine (hemiaminal) H :0: H o: H Ö: H 0: H H .Ph Ph PhCH H,Ñ-Ph Ph Ph Ph Ph - H H. нн H2N-Ph non-productive side reaction H* - H H H H-O: H Ph - H20 Ph S Ph Ph Ph Ph :B H. Imine Iminium ion

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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