(D) Another repeating transformation is the reductive amination that shows up in the Schemes 3, 5 and 6. This takes Ar-NH₂ to Ar-N(CH3)2 with NaBH4/HCHO (formaldedyde). This provides the "rear" dipole that drives the nanocar. Show the mechanism for converting Ar-NH₂ → Ar-N(CH3)2 with two formaldehyde molecules and NaBH4. You will need to review your notes from lab5 in

(D) Another repeating transformation is the reductive amination that shows up in the Schemes 3, 5 and 6. This takes Ar-NH₂ to Ar-N(CH3)2 with NaBH4/HCHO (formaldedyde). This provides the "rear" dipole that drives the nanocar. Show the mechanism for converting Ar-NH₂ → Ar-N(CH3)2 with two formaldehyde molecules and NaBH4. You will need to review your notes from lab5 in

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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