Answer the questions below based on the spectraWrite a mechanism for the formation of semicarbazones. Suggest a reason why the NH2 group depicted in the reaction scheme is the one used to form the semicarbazone and not the other NH2 group. Yes, the answer is resonance, but you really want to explain how resonance affects the reactivity of the non-reacting NH2 group. Explain why the 2,4-dintrophenylhydrazone is colored and the semicarbazide is not. The reason should relate to the structure. What would be produced if the 2,4-dinitrophenylhydrazone was prepared in the presence of NaBH3CN? 1.0011.411.311.211.111.010.910.810.710.610.510.410.310.210.110.0 0.893.008.48.38.28.18.07.97.8777.67.5707.47.37.27.1

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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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Answer the questions below based on the spectra

Write a mechanism for the formation of semicarbazones.
Suggest a reason why the NH2 group depicted in the reaction scheme is the one used to form the semicarbazone and not the other NH2 group. Yes, the answer is resonance, but you really want to explain how resonance affects the reactivity of the non-reacting NH2 group.
Explain why the 2,4-dintrophenylhydrazone is colored and the semicarbazide is not. The reason should relate to the structure.

What would be produced if the 2,4-dinitrophenylhydrazone was prepared in the presence of NaBH3CN?

1.00
11.4
11.3
11.2
11.1
11.0
10.9
10.8
10.7
10.6
10.5
10.4
10.3
10.2
10.1
10.0

0.89
3.00
8.4
8.3
8.2
8.1
8.0
7.9
7.8
77
7.6
7.5
70
7.4
7.3
7.2
7.1

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