Please help with question 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

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Please help with question 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 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-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
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 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-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
Expt. #2: Electrophilic aromatic nitration of an
unknown monosubstituted benzene
G
HNO3 (conc.), H₂SO4 (conc.)
G
ortho or meta
or para isomer
NO₂
Transcribed Image Text:Expt. #2: Electrophilic aromatic nitration of an unknown monosubstituted benzene G HNO3 (conc.), H₂SO4 (conc.) G ortho or meta or para isomer NO₂
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