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Please explain question 1 and 8  1. How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material? 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) Thank you!

Please explain question 1 and 8  1. How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material? 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) Thank you!

Chemistry
Chemistry
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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
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Please explain question 1 and 8 

1. How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material?

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)

Thank you!

(1) (2) 3 (4) (5) (6) (7) (8) (9) (10) 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 answer 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 -O-H What was the mp range you observed for your mononitrated reaction product? Leave this space blank if you either obtained no product or did not run the reaction. What is the reported (literature) mp range of your mononitrated reaction product? Cite the reference from which you obtained the literature mp range. C8H9NO 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 114.2 degrees C 113-115 degrees C
Transcribed Image Text:(1) (2) 3 (4) (5) (6) (7) (8) (9) (10) 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 answer 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 -O-H What was the mp range you observed for your mononitrated reaction product? Leave this space blank if you either obtained no product or did not run the reaction. What is the reported (literature) mp range of your mononitrated reaction product? Cite the reference from which you obtained the literature mp range. C8H9NO 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 114.2 degrees C 113-115 degrees C
Expt. #2: Electrophilic aromatic nitration of an unknown monosubstituted benzene (1) (2) (3) (4) (5) (6) (7) (8) (9) (10) G HNO3 (conc.), H₂SO4 (conc.) 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 answer 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 What was the mp range you observed for your mononitrated reaction product? Leave this space blank if you either obtained no product or did not run the reaction. What is the reported (literature) mp range of your mononitrated reaction product? Cite the reference from which you obtained the literature mp range. G NO₂ ortho or meta or para isomer Place your answers in the spaces below C8H9NO 5 an O-H bond: No an N-H bond: Yes a C=O (carbonyl): Yes 6 Yes 169.48 ppm 24.18 ppm 114.2 degrees C 113-115 degrees C pts 2 2 2 2 3 3 2 2 5 2 2
Transcribed Image Text:Expt. #2: Electrophilic aromatic nitration of an unknown monosubstituted benzene (1) (2) (3) (4) (5) (6) (7) (8) (9) (10) G HNO3 (conc.), H₂SO4 (conc.) 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 answer 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 What was the mp range you observed for your mononitrated reaction product? Leave this space blank if you either obtained no product or did not run the reaction. What is the reported (literature) mp range of your mononitrated reaction product? Cite the reference from which you obtained the literature mp range. G NO₂ ortho or meta or para isomer Place your answers in the spaces below C8H9NO 5 an O-H bond: No an N-H bond: Yes a C=O (carbonyl): Yes 6 Yes 169.48 ppm 24.18 ppm 114.2 degrees C 113-115 degrees C pts 2 2 2 2 3 3 2 2 5 2 2
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