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 := C8H9NOHow many degrees of unsaturation are present in your unknown monosubstitutedbenzene 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 startingmaterial contain any of the following structural features (for each choice indicate eitherYES or NO):Based on its ¹³C NMR spectrum, how many types of carbon (i.e., sets of equivalentcarbons) are there in your unknown monosubstituted benzene starting material?How many different sets of equivalent aromatic (benzene ring) carbons can be seen inthe ¹³C NMR spectrum of your unknown monosubstituted benzene starting material?Are there any peaks for non-aromatic carbons in the ¹³C NMR spectrum of yourunknown monosubstituted benzene starting material (yes or no)?If your answer to question 6 is "yes", list the corresponding ppm value(s) for anynon-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 providede.g., if G was a hydroxyl group you would draw-HPlace your answers inthe spaces below5an O-H bond: Noan N-H bond: Yesa C=O (carbonyl): Yes64Yes169.48 ppm24.18 ppm Expt. #2: Electrophilic aromatic nitration of anunknown monosubstituted benzeneGHNO3 (conc.), H₂SO4 (conc.)Gortho or metaor para isomerNO₂

In aromatic Electrophilic substitution reactions H of the benzene ring is replaced by incoming…

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

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

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter2: Alkanes And Cycloalkanes

Section: Chapter Questions

Problem 2.58P: Following are structural formulas and heats of combustion of acetaldehyde and ethylene oxide. Which...

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Concept explainers

Electronic Effects

The effect of electrons that are located in the chemical bonds within the atoms of the molecule is termed an electronic effect. The electronic effect is also explained as the effect through which the reactivity of the compound in one portion is controlled by the electron repulsion or attraction producing in another portion of the molecule.

Drawing Resonance Forms

In organic chemistry, resonance may be a mental exercise that illustrates the delocalization of electrons inside molecules within the valence bond theory of octet bonding. It entails creating several Lewis structures that, when combined, reflect the molecule's entire electronic structure. One Lewis diagram cannot explain the bonding (lone pair, double bond, octet) elaborately. A hybrid describes a combination of possible resonance structures that represents the entire delocalization of electrons within the molecule.

Using Molecular Structure To Predict Equilibrium

Equilibrium does not always imply an equal presence of reactants and products. This signifies that the reaction reaches a point when reactant and product quantities remain constant as the rate of forward and backward reaction is the same. Molecular structures of various compounds can help in predicting equilibrium.

Question

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

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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