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 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-O-HWhat 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.C8H9NO5an O-H bond: Noan N-H bond: Yesa C=O (carbonyl):Yes64Yes169.48 ppm24.18 ppm114.2degrees C113-115degrees C Expt. #2: Electrophilic aromatic nitration of anunknown monosubstituted benzene(1)(2)(3)(4)(5)(6)(7)(8)(9)(10)GHNO3 (conc.), H₂SO4 (conc.)How 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 {-0-HWhat 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.GNO₂ortho or metaor para isomerPlace your answers inthe spaces belowC8H9NO5an O-H bond: Noan N-H bond: Yesa C=O (carbonyl): Yes6Yes169.48 ppm24.18 ppm114.2degrees C113-115degrees Cpts22223322522

Benzene undergo Electrophilic substitution reaction in which an electrophile replaces H of its ring.

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!

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

Chapter22: Reactions Of Benzene And Its Derivatives

Section: Chapter Questions

Problem 22.59P

See similar textbooks

Similar questions

Why methyl benzoate is mainly meta orienting? Explain it with the help of charge formation in the benzene ring ( ortho, meta and para position) Show Structures in methylbenzoate.
A student was given from the list of the compounds below A, B and D blindly and asked to identify them all. He treated each of them with Brady's reagent (2,4-ditrophenylhydrazine) and isolated a bright yellow compound for one of them, but the other two gave false negatives. The student reasoned that the false negatives may be due to sterics and, on further thinking, it dawned on him that he might be able to rule out one of the false negatives with the haloform test. What compound did he find compatible with the haloform test? That compound did indeed give a false negative in the Brady test. Which of the other two was positive in the Brady test? A = haloform B = Brady A = haloform D = Brady B = haloform A = Brady B = haloform D = Brady D = haloform A = Brady D = haloform B = Brady
When the nitrogen-containing aromatic heterocyclic compounds 1 and 2 are treated with HCl, only 1 forms the hydrochloride salt, whereas compound 2 is unreactive. Provide an explanation for this observed reactivity.
Predict whether the cyclic system is aromatic , anti-aromatic, or non-aromatic by counting electrons and explain why ? Also circle all the basic nitrogen’s wherever possible . Show all lone pairs which are involved in cyclic delocalization?
Write down the explicit structures of A, B, C and D in accordance with the reactions given in the synthesis plan, which shows the synthesis of D, a pheromone of moth.
Show the electron-flow mechanism of the synthetic schemes (R-Salsolinol) of the picture below. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.
Give a clear handwritten answer with explanation....complete the following reactions with missing reagents...
Kepone, aldrin, and chlordane are synthesized from hexachlorocyclopentadiene and other five-membered-ring compounds. Show how these three pesticides are composed of two five-membered rings.
While dehydrating 2-Methlycyclohexanol to 1-Methlycyclohexanol, and 3-Methlycyclohexanol 1)what is the common problem associate with E1 reaction? Discuss the intermediate. 2) Briefly compare and contrast E1 vs E2 Elimination reactions. INclude details such as speed of the reactions in relation to each other, rate-determining steps (E1), and stereochemical requirements (E2). Mention whether the steps of the reactions are reversible and discuss the conditions that can drive the equilibrium to favor product formation.
(a) Illustrate the following name reactions by giving example :(i) Cannizzaro’s reaction(ii) Clemmensen reduction(b) An organic compound A contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollen’s reagent but forms an addition compound with sodium hydrogen sulphite and gives positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acids. Derive the possible structure of compound A.
Q1. Outline two methods of phenols synthesis. Q2. Give a concise account on the nomenclature of heterocyclic compound.
Compound F may be synthesised by the method attached: When 2-chloropropane treated with NaOH and 1-chloropropane treated with NaOH separately produce two different functional groups. Provide both reactions and explain the two different functional groups produced.