Your organic chemistry study partner attempts the following reaction between a Grignard reagent and benzaldehyde. Unfortunately, your study partner does not form the desired product. Instead, a different product forms with the following 13C NMR signals: 73, 35, 23. In part 1, draw the desired product your study partner was trying to form. In part 2, draw the actual product that forms under these conditions. Be sure your answers account for stereochemistry, where appropriate. If multiple stereoisomers form, be sure to draw all possible products using appropriate wedges and dashes. Br 1. Mg 3. H₂O

Your organic chemistry study partner attempts the following reaction between a Grignard reagent and benzaldehyde. Unfortunately, your study partner does not form the desired product. Instead, a different product forms with the following 13C NMR signals: 73, 35, 23. In part 1, draw the desired product your study partner was trying to form. In part 2, draw the actual product that forms under these conditions. Be sure your answers account for stereochemistry, where appropriate. If multiple stereoisomers form, be sure to draw all possible products using appropriate wedges and dashes. Br 1. Mg 3. H₂O

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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Concept explainers

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

Question

Your organic chemistry study partner attempts the following reaction between a Grignard reagent and benzaldehyde. Unfortunately, your study
partner does not form the desired product. Instead, a different product forms with the following 13C NMR signals: 73, 35, 23.
In part 1, draw the desired product your study partner was trying to form. In part 2, draw the actual product that forms under these conditions. Be
sure your answers account for stereochemistry, where appropriate. If multiple stereoisomers form, be sure to draw all possible products using
appropriate wedges and dashes.
1.
Mg
3. H₂O*

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Answer both parts of the question and show your work please.