Exam (elaborations)
Chapter 13 - Electrophilic and Nucleophilic Aromatic Substitution (Test Bank)
- Course
- Institution
Organic Chemistry 10th Edition by Francis Carey - Test Bank
[Show more]
Seller
Follow
premiumbiz379
Reviews received
Content preview
1. What is the product of the following reaction?A. isobutylbenzene
B. sec-butylbenzene
C. 2-methyl-1-phenylpropene
D. tert-butylbenzene
Bloom's Level: 3. Apply
Chapter: 13
Difficulty: Hard
Gradable: automatic
Section: 13.06
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
2. The major product(s) in the nitration of benzoic acid is(are)
A. mixture of ortho and para-nitrobenzoic acid.
B. nitrobenzene.
C. meta-nitrobenzoic acid.
D. nitrobenzene and para-nitrobenzoic acid.
Accessibility: Keyboard Navigation
Bloom's Level: 3. Apply
Chapter: 13
Difficulty: Medium
Gradable: automatic
Section: 13.13
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
13-1
Copyright © 2016 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of
McGraw-Hill Education.
,3. Which of the following aromatic compounds reacts faster than benzene in electrophilic
aromatic bromination?
A. A
B. B
C. C
D. D
Bloom's Level: 4. Analyze
Chapter: 13
Difficulty: Medium
Gradable: automatic
Section: 13.12
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
4. Nitration of benzoic acid has a reaction rate which is __________ than the nitration rate
of benzene and gives primarily the _____________ product(s).
A. slower, meta
B. faster, ortho, para
C. slower, ortho, para
D. faster, meta
Accessibility: Keyboard Navigation
Bloom's Level: 2. Understand
Chapter: 13
Difficulty: Medium
Gradable: automatic
Section: 13.13
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
13-2
Copyright © 2016 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of
McGraw-Hill Education.
,5. Which one of the following is the electrophile in the reaction shown below?
A. benzene
B. NO3¯
C. NO2+
D. H2SO4
Bloom's Level: 1. Remember
Chapter: 13
Difficulty: Easy
Gradable: automatic
Section: 13.03
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
6. What is the electrophile in the Friedel-Crafts alkylation reaction below?
A. AlCl3
B. Cl¯
C. benzene
+
D. (CH3)3C
Bloom's Level: 2. Understand
Chapter: 13
Difficulty: Easy
Gradable: automatic
Section: 13.06
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
13-3
Copyright © 2016 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of
McGraw-Hill Education.
, 7. Which point on the potential energy diagram corresponds to the species shown to the
right for the electrophilic bromination of benzene with Br 2/FeBr3?
A. A
B. B
C. C
D. D
Bloom's Level: 2. Understand
Chapter: 13
Difficulty: Medium
Gradable: automatic
Section: 13.05
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
8. Which species below best depicts the electrophile in the FeBr 3-catalyzed bromination of
benzene?
A. Br2
B. FeBr4-
C.
D. FeBr3
Bloom's Level: 1. Remember
Chapter: 13
Difficulty: Easy
Gradable: automatic
Section: 13.05
Subtopic: Electrophilic aromatic substitution (EAS) reactions
Topic: Aromatic Compounds
13-4
Copyright © 2016 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of
McGraw-Hill Education.
The benefits of buying summaries with Stuvia:
Guaranteed quality through customer reviews
Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.
Quick and easy check-out
You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.
Focus on what matters
Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!
Frequently asked questions
What do I get when I buy this document?
You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.
Satisfaction guarantee: how does it work?
Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.
Who am I buying these notes from?
Stuvia is a marketplace, so you are not buying this document from us, but from seller premiumbiz379. Stuvia facilitates payment to the seller.
Will I be stuck with a subscription?
No, you only buy these notes for $5.84. You're not tied to anything after your purchase.
Can Stuvia be trusted?
4.6 stars on Google & Trustpilot (+1000 reviews)
77254 documents were sold in the last 30 days
Founded in 2010, the go-to place to buy study notes for 14 years now