
(a)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration.

Answer to Problem 23.49P
The sulfuric acid should not be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is activated.
Explanation of Solution
The given
In this aromatic compound, the benzene ring has two methyl groups attached. The alkyl groups are electron donating inductively, thus increases the electron density around the ring and activates it. As the ring is electron rich and activated it can undergo nitration on reaction with concentrated nitric acid and there is no need to add sulfuric acid.
It is determined that the nitration of a given compound can be carried out with concentrated nitric acid only and no need to add sulfuric acid based on the activation of aromatic ring.
(b)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound, it is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration.

Answer to Problem 23.49P
The sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is deactivated.
Explanation of Solution
The given aromatic compound is:
In this aromatic compound, the benzene ring has two carbonyl groups attached. The carbonyl groups have electron withdrawing resonance effect, thus decreases the electron density around the ring and deactivates it. As the ring is electron poor and deactivated, the sulfuric acid should be added to nitric acid to carry out the nitration.
It is determined that the nitration of a given compound can be carried by addition of sulfuric acid to nitric acid based on deactivation of aromatic ring.
(c)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound, it is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration.

Answer to Problem 23.49P
The sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is deactivated.
Explanation of Solution
The given aromatic compound is:
In this aromatic compound, the benzene ring has nitrile group attached. The nitrile group have electron withdrawing resonance effect, thus decreases the electron density around the ring and deactivates it. As the ring is electron poor and deactivated, the sulfuric acid should be added to nitric acid to carry out the nitration.
It is determined that the nitration of a given compound can be carried by addition of sulfuric acid to nitric acid based on deactivation of aromatic ring.
(d)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound, it is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration. The resonance effect is predominant over inductive effect due to actual delocalization of pi electrons.

Answer to Problem 23.49P
The sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is deactivated.
Explanation of Solution
The given aromatic compound is:
In this aromatic compound, the benzene ring has
It is determined that the nitration of a given compound can be carried by addition of sulfuric acid to nitric acid based on deactivation of aromatic ring.
(e)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound, it is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration.

Answer to Problem 23.49P
The sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is deactivated.
Explanation of Solution
The given aromatic compound is:
In this aromatic compound, the benzene ring has
It is determined that the nitration of a given compound can be carried by addition of sulfuric acid to nitric acid based on deactivation of aromatic ring.
(f)
Interpretation:
Whether sulfuric acid should be added to concentrated nitric acid to carry out a nitration on given compound, it is to be determined.
Concept introduction:
The nitration is the electrophilic aromatic substitution reaction. The aromatic ring on reaction with nitric acid or with a mixture of concentrated nitric acid and sulfuric acid undergoes substitution of one of the ring hydrogen by nitro group and forms nitrobenzene, this is called nitration. The selection of reagent either nitric acid or mixture of nitric acid and sulfuric acid is depends on whether the aromatic ring is activated or deactivated. The electron donating groups increases the electron density around the ring and activates it whereas the electron withdrawing groups decrease the electron density around the ring and deactivates it. The activated aromatic ring can undergo nitration on reaction with nitric acid. The deactivated ring required addition of sulfuric acid to nitric acid to undergo nitration.

Answer to Problem 23.49P
The sulfuric acid should not be added to concentrated nitric acid to carry out a nitration on given compound as the aromatic ring is activated.
Explanation of Solution
The given aromatic compound is:
In this aromatic compound, the benzene ring has one methyl and one methoxy groups attached. The alkyl groups are electron donating inductively and methoxy group has electron donating resonance effect, thus increases the electron density around the ring and activates it. As the ring is electron rich and activated it can undergo nitration on reaction with concentrated nitric acid and there is no need to add sulfuric acid.
It is determined that the nitration of a given compound can be carried out with concentrated nitric acid only and no need to add sulfuric acid based on the activation of aromatic ring.
Want to see more full solutions like this?
Chapter 23 Solutions
Organic Chemistry: Principles And Mechanisms
- Assign these C-NMR and H-NMR Spectrumarrow_forwardPredict the product of this organic reaction: IZ + HO i P+H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. No Answer Click and drag to start drawing a structure. ☐ :arrow_forwardPredict the products of this organic reaction: 0 O ----- A + KOH ? CH3-CH2-C-O-CH2-C-CH3 Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click anywhere to draw the first atom of your structure. X ⑤ èarrow_forward
- Predict the products of this organic reaction: O CH3 + H2O + HCI A A? CH3-CH2-C-N-CH3 Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No Reaction Click anywhere to draw the first atom of your structure.arrow_forwardWhat is the missing reactant in this organic reaction? R+ HO-C-CH2-CH3 0= CH3 CH3 —CH, C−NH—CH CH3 + H₂O Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. No Answer Click anywhere to draw the first atom of your structure. €arrow_forward个 CHEM&131 9267 - $25 - Intro to Mail - Hutchison, Allison (Student x Aktiv Learnin https://app.aktiv.com Draw the product of the reaction shown below. Ignore inorganic byproducts. + Na2Cr2O7 Acetone, H2SO4 Type here to search Dryng OH W Prarrow_forward
- Predict the products of this organic reaction: OH + NaOH A? Specifically, in the drawing area below draw the skeletal ("line") structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click and drag to start drawing a structure. ✓ Sarrow_forwardPredict the products of this organic reaction: CH3-C-O-CH2-CH2-C-CH3 + H₂O ? A Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click anywhere to draw the first atom of your structure. :☐ darrow_forwardDE d. Draw an arrow pushing mechanism for the following IN O CI N fo 人 P Polle DELL prt sc home end ins F5 F6 F7 F8 F9 F10 F11 F12arrow_forward
- Predict the products of this organic reaction: + H₂O H* ? A Specifically, in the drawing area below draw the skeletal ("line") structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No Reaction Click and drag to start drawing a structure.arrow_forwardPredict the major organic products of the reaction below and draw them on right side of the arrow. If there will be no significant reaction, check the box below the drawing area instead. C Cl CH, OH There will be no significant reaction. + pyridine G Click and drag to start drawing a structure.arrow_forwardWhat is the missing reactant in this organic reaction? H R+ H2O Δ OH 0= CH3-CH-O-CH3 + CH3-C-OH Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. No Answer Click anywhere to draw the first atom of your structure. dyarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





