ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<
ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<
5th Edition
ISBN: 9781260293685
Author: SMITH
Publisher: MCGRAW-HILL CUSTOM PUBLISHING
bartleby

Concept explainers

Question
Book Icon
Chapter 18, Problem 18.21P
Interpretation Introduction

(a)

Interpretation: The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are to be drawn.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.

Expert Solution
Check Mark

Answer to Problem 18.21P

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Explanation of Solution

The Friedel-craft alkylation of aromatic compound with CH3Cl in presence of AlCl3 involves substitution of CH3 group. Friedel-craft alkylation reaction does not take place when an aromatic ring is substituted by a strong electron releasing or strong electron withdrawing group.

The structure of given compound shows that benzene ring is substituted by SO3H group. This group is strong electron withdrawing group. Hence, the Friedel-craft alkylation reaction will not take place on reaction of given compound with CH3Cl and AlCl3.

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 18, Problem 18.21P , additional homework tip  1

Figure 1

Conclusion

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Interpretation Introduction

(b)

Interpretation: The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are to be drawn.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.

Expert Solution
Check Mark

Answer to Problem 18.21P

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Explanation of Solution

The Friedel-craft alkylation of aromatic compound with CH3Cl in presence of AlCl3 involves substitution of CH3 group. Friedel-craft alkylation reaction does not take place when an aromatic ring is substituted by a strong electron releasing or strong electron withdrawing group.

The structure of given compound shows that benzene ring is substituted by Cl group. This group is a strong deactivating group. Hence, the Friedel-craft alkylation reaction will not take place on reaction of given compound with CH3Cl and AlCl3.

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 18, Problem 18.21P , additional homework tip  2

Figure 2

Conclusion

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Interpretation Introduction

(c)

Interpretation: The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are to be drawn.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.

Expert Solution
Check Mark

Answer to Problem 18.21P

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Explanation of Solution

The Friedel-craft alkylation of aromatic compound with CH3Cl in presence of AlCl3 involves substitution of CH3 group. Friedel-craft alkylation reaction does not take place when an aromatic ring is substituted by a strong electron releasing or strong electron withdrawing group.

The structure of given compound shows that benzene ring is substituted by N(CH3)2 group. This group is a strong electron releasing group. Hence, the Friedel-craft alkylation reaction will not take place on reaction of given compound with CH3Cl and AlCl3.

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 18, Problem 18.21P , additional homework tip  3

Figure 3

Conclusion

The given compound does not undergo Friedel-craft alkylation reaction on reaction with CH3Cl and AlCl3.

Interpretation Introduction

(d)

Interpretation: The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are to be drawn.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.

Expert Solution
Check Mark

Answer to Problem 18.21P

The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are drawn below.

Explanation of Solution

The Friedel-craft alkylation of aromatic compound with CH3Cl in presence of AlCl3 involves substitution of CH3 group. Friedel-craft alkylation reaction does not take place when an aromatic ring is substituted by a strong electron releasing or strong electron withdrawing group.

The structure of given compound shows that benzene ring is substituted by NHCOCH3 group. This group is moderately electron releasing group. Hence, the given compound undergoes Friedel-craft alkylation reaction with CH3Cl and AlCl3 as shown in Figure 4.

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 18, Problem 18.21P , additional homework tip  4

Figure 4

Conclusion

The products formed by the Friedel-Craft alkylation of given compound with CH3Cl and AlCl3 are shown in Figure 4.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
#20 B Draw structural formulas for all possible carbocations formed by the reaction of each alkene with HCl.
n-Butyl methyl ether is an isomer of MTBE and has a boiling point of 70 oC. Explain why the boiling point is significantly different compared to MTBE.
Draw the product formed when C6H5N2+Cl− reacts with each compound.

Chapter 18 Solutions

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<

Ch. 18 - Prob. 18.11PCh. 18 - Prob. 18.12PCh. 18 - Prob. 18.13PCh. 18 - Problem 18.14 Draw all resonance structures for...Ch. 18 - Problem 18.15 Classify each substituent as...Ch. 18 - Prob. 18.16PCh. 18 - Problem 18.17 Label each compound as more or less...Ch. 18 - Problem 18.18 Rank the following compounds in...Ch. 18 - Prob. 18.19PCh. 18 - Problem 18.20 Draw the products of each...Ch. 18 - Prob. 18.21PCh. 18 - Problem 18.22 Draw the products formed when each...Ch. 18 - Problem 18.23 Devise a synthesis of each compound...Ch. 18 - Problem 18.24 Draw the products of each...Ch. 18 - Problem 18.25 Draw a stepwise mechanism for the...Ch. 18 - Problem 18.26 Draw the products of each...Ch. 18 - Prob. 18.27PCh. 18 - Prob. 18.28PCh. 18 - Problem 18.29 How could you use ethylbenzene to...Ch. 18 - Prob. 18.30PCh. 18 - Problem 18.31 What steps are needed to convert...Ch. 18 - Problem 18.32 Synthesize each compound from...Ch. 18 - Problem 18.33 Synthesize each compound from...Ch. 18 - Prob. 18.34PCh. 18 - 18.35 What is the major product formed by an...Ch. 18 - 18.36 Draw the products formed when phenol is...Ch. 18 - Problem 18.37 Draw the products formed when each...Ch. 18 - 18.38 Draw the products of each reaction. a. d....Ch. 18 - 18.39 What products are formed when benzene is...Ch. 18 - 18.40 Draw the products of each reaction. c. d....Ch. 18 - 18.41 You have learned two ways to make an alkyl...Ch. 18 - 18.42 Draw the structure of A, an intermediate in...Ch. 18 - Prob. 18.43PCh. 18 - Prob. 18.44PCh. 18 - 18.45 Explain why each of the following reactions...Ch. 18 - Prob. 18.46PCh. 18 - 18.47 For each of the following substituted...Ch. 18 - 18.48 Consider the tetracyclic aromatic compound...Ch. 18 - 18.49 For each N-substituted benzene, predict...Ch. 18 - Prob. 18.50PCh. 18 - 18.51 Using resonance structures, explain why a...Ch. 18 - Prob. 18.52PCh. 18 - 18.53 Rank the aryl halides in each group in order...Ch. 18 - 18.54 Draw a stepwise mechanism for the following...Ch. 18 - Prob. 18.55PCh. 18 - 18.56 Draw a stepwise, detailed mechanism for the...Ch. 18 - Prob. 18.57PCh. 18 - 18.58 Draw a stepwise mechanism for the following...Ch. 18 - Prob. 18.59PCh. 18 - Prob. 18.60PCh. 18 - Prob. 18.61PCh. 18 - Prob. 18.62PCh. 18 - 18.63 Synthesize each compound from benzene and...Ch. 18 - Problem 18.64 Synthesize each compound from...Ch. 18 - Prob. 18.65PCh. 18 - Prob. 18.66PCh. 18 - Prob. 18.67PCh. 18 - Prob. 18.68PCh. 18 - Problem 18.69 Identify the structures of isomers A...Ch. 18 - Prob. 18.70PCh. 18 - Problem 18.71 Compound X (molecular formula ) was...Ch. 18 - 18.72 Reaction of p-cresol with two equivalents of...Ch. 18 - Prob. 18.73PCh. 18 - The NMR spectrum of phenol () shows three...Ch. 18 - Explain the reactivity and orientation effects...Ch. 18 - Prob. 18.76PCh. 18 - Prob. 18.77PCh. 18 - Prob. 18.78PCh. 18 - Prob. 18.79P
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning