PKG ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259963667
Author: SMITH
Publisher: MCG
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Textbook Question
Chapter 18, Problem 18.53P
Rank the aryl halides in each group in order of increasing reactivity in nucleophilic
a. chlorobenzene, p-fluoronitrobenzene, m-fluoronitrobenzene
b.
c.
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Which of the following is expected to be the MOST reactive towards electrophilic aromatic substitution?
a. p-Cresol
b. p-Toluidine
c. p-Chlorophenol
d.p-Chloroaniline
2. Which of the following is expected to be the LEAST reactive towards electrophilic aromatic substitution?
a. p-Hydroxybenzoic acid
b. p-Methoxybenzoic acid
c. p-Aminophenyl acetate
d. p-Methoxyphenyl acetate
d.
12. What is the simplest fused aromatic hydrocarbon?
a. Naphthalene
b. 1,2-Benzylpyrene
c. Methylbenzene
d. Cyclobenzene
13. In electrophilic aromatic substitution reactions, a phenyl substituent on the
aromatic ring is
a. a deactivator and a m-director
b. a deactivator and an o,p-director
c. an activator and an o,p-director
d. none of the above
14. Acetylide ion formation requires a strong base like NaNH2 which in turn is made
using ammonia and Na. The catalyst used in this reaction is
a. Cu
b. Fe
C. Pt
d. Pd
15. Hydroboration-Oxidation of terminal alkyne results in the formation of an
a. Aldehyde by Markovnikov mechanism
b. Ketone by anti-Markovnikov mechanism
c. Enol by Markovnikov mechanism
d. Aldehyde by anti-Markovnikov mechanism
16.p-Methoxybenzaldehyde can be prepared from anisole using the Gatterman-
Koch formylation. What mixture of reagents is necessary for this process?
a. CO, HCI, AICI3, CuCI
b. CO, SO3, H2SO4
CO2, HCI, AICI3
d. CO2, SO3, H2SO4
e. CO2, HNO3, H2SO4
C.
What is the first step in the general mechanism for electrophilic aromatic substitution?
a. aromatic ring protonation
b.loss of the electrophilic aromatic ring
c. deprotonation of the aromatic ring
d.addition of the electrophilic to the aromatic ring.
Chapter 18 Solutions
PKG ORGANIC CHEMISTRY
Ch. 18 - Prob. 18.1PCh. 18 - Prob. 18.2PCh. 18 - Prob. 18.3PCh. 18 - Prob. 18.4PCh. 18 - Prob. 18.5PCh. 18 - Prob. 18.6PCh. 18 - Prob. 18.7PCh. 18 - Prob. 18.8PCh. 18 - Problem 18.9 Draw the product of each reaction
a....Ch. 18 - Prob. 18.10P
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
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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
- 1. Which is the strongest base? NH2 „NH2 NH2 `NH2 b. O,N C. d. а. 2. Which of the following compounds is the least reactive towards a nucleophilic addition reaction? a. 3-Methyl-2-butanone b. 2,4-Dimethylpentan-3-one C. Acetone d. Methanalarrow_forwardNB: All bonds to benzene must be made using Electrophilic Aromatic Substitution (including Friedel-Crafts reactions) or Nucleophilic Aromatic Substitution! Design a synthesis of each of the following target molecules, starting with benzene: a. pentylbenzene b. 2-chloro-1-propyl benzene d. 3-chloro-1-propyl benzene d. 1-phenyl-1-butanolarrow_forwardWhat would be the effect on the rate of reaction if the concentration of the nucleophile weredoubled in an…a. SN1 reaction? Briefly explain.b. SN2 reaction? Briefly explain.arrow_forward
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