Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Question

Hi can you please help with with questions 2 and 8. Thank you so much!

 

2. What is the molecular formula of your mononitrated reaction product?

8. Based on all of the data provided, what is the identity of the “G” group? Please NEATLY & CLEARLY draw its full Lewis structure in the space provided

(1) (2) (3) (4) (5) (6) (7) (8) Starting material = C8H9NO How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material? Do not show calculations. What is the molecular formula of your mononitrated reaction product? How many degrees of unsaturation are present in your mononitrated reaction product? Do not show calculations. Based on its IR spectrum, does your unknown monosubstituted benzene starting material contain any of the following structural features (for each choice indicate either YES or NO): Based on its ¹³C NMR spectrum, how many types of carbon (i.e., sets of equivalent carbons) are there in your unknown monosubstituted benzene starting material? How many different sets of equivalent aromatic (benzene ring) carbons can be seen in the ¹3C NMR spectrum of your unknown monosubstituted benzene starting material? Are there any peaks for non-aromatic carbons in the ¹3C NMR spectrum of your unknown monosubstituted benzene starting material (yes or no)? If your answer to question 6 is "yes", list the corresponding ppm value(s) for any non-aromatic carbon(s)? If your answer to question 6 is "no", leave the ans ver space blank. Based on all of the data provided, what is the identity of the "G" group? Please NEATLY & CLEARLY draw its full Lewis structure in the space provided e.g., if G was a hydroxyl group you would draw {0-H Place your answers in the spaces below 5 an O-H bond: No an N-H bond: Yes a C=O (carbonyl): Yes 6 4 Yes 169.48 ppm 24.18 ppm
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Transcribed Image Text:(1) (2) (3) (4) (5) (6) (7) (8) Starting material = C8H9NO How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material? Do not show calculations. What is the molecular formula of your mononitrated reaction product? How many degrees of unsaturation are present in your mononitrated reaction product? Do not show calculations. Based on its IR spectrum, does your unknown monosubstituted benzene starting material contain any of the following structural features (for each choice indicate either YES or NO): Based on its ¹³C NMR spectrum, how many types of carbon (i.e., sets of equivalent carbons) are there in your unknown monosubstituted benzene starting material? How many different sets of equivalent aromatic (benzene ring) carbons can be seen in the ¹3C NMR spectrum of your unknown monosubstituted benzene starting material? Are there any peaks for non-aromatic carbons in the ¹3C NMR spectrum of your unknown monosubstituted benzene starting material (yes or no)? If your answer to question 6 is "yes", list the corresponding ppm value(s) for any non-aromatic carbon(s)? If your answer to question 6 is "no", leave the ans ver space blank. Based on all of the data provided, what is the identity of the "G" group? Please NEATLY & CLEARLY draw its full Lewis structure in the space provided e.g., if G was a hydroxyl group you would draw {0-H Place your answers in the spaces below 5 an O-H bond: No an N-H bond: Yes a C=O (carbonyl): Yes 6 4 Yes 169.48 ppm 24.18 ppm
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