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CHEM 334 Lab Final – Verified Questions & Answers | Certification Ready.

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What is the first step in the general mechanism for electrophilic aromatic substitution? - Correct Answer: addition of the electrophile to the aromatic ring What are the two effects that have to be considered to determine the influence a substituent will have on electrophilic aromatic substitution? - Correct Answer: inductive and resonance Why is the nitro group a meta director? - Correct Answer: because it removes more electron density from the ortho and para positions than the met position, thus deactivating the meta position less What is the electrophile in aromatic nitration? - Correct Answer: NO2+ What is the driving force for losing a proton as the last step in electrophilic aromatic substitution? - Correct Answer: to reform an aromatic system Why is sulfuric acid used in aromatic substitution? - Correct Answer: to form the active electrophile NO2+ Of the compounds listed, which would be the most reactive toward alkylation? - Correct Answer: aromatic ring with NH2

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CHEM 334 Lab Final – Verified Questions &
Answers | Certification Ready.
What is the first step in the general mechanism for electrophilic aromatic
substitution? - Correct Answer>>>: addition of the electrophile to the
aromatic ring


What are the two effects that have to be considered to determine the influence
a substituent will have on electrophilic aromatic substitution? - Correct
Answer>>>: inductive and resonance


Why is the nitro group a meta director? - Correct Answer>>>: because
it removes more electron density from the ortho and para positions than the
met position, thus deactivating the meta position less


What is the electrophile in aromatic nitration? - Correct Answer>>>:
NO2+


What is the driving force for losing a proton as the last step in electrophilic
aromatic substitution? - Correct Answer>>>: to reform an aromatic
system


Why is sulfuric acid used in aromatic substitution? - Correct Answer>>>:
to form the active electrophile NO2+


Of the compounds listed, which would be the most reactive toward alkylation? -
Correct Answer>>>: aromatic ring with NH2


Rank the following compounds in order of increasing reactivity toward
electrophilic aromatic substitution. - Correct Answer>>>: B>A>C

Page 1 of 10

, CHEM 334 Lab Final – Verified Questions &
Answers | Certification Ready.

What is the electrophile in the Friedel Crafts alkylation reaction with tert-butyl
alcohol? - Correct Answer>>>: tert butyl cation


Arrange the following compounds in order of decreasing reactivity in
electrophilic substitution. - Correct Answer>>>: II>V>III>I>IV


Which of the following statements is (are) true about electrophilic aromatic
substitution? - Correct Answer>>>: the methoxy group, -OCH3, is an o-
p activator because of a strong electron donating effect


What is a major problem with Friedel-Crafts alkylation? - Correct Answer>>>:
you frequently get over-alkylation


Indicate which of the following acids could be used in the Friedel Crafts
alkylation? - Correct Answer>>>: all of the above


Which of the following reactions would yield isopropyl benzene as the major
product? - Correct Answer>>>: benzene + (CH3)2CH2Cl and AlCl3


Indicate the correct steps that will initiate the Grignard reaction. - Correct
Answer>>>: all of the above


Why do we use anhydrous diethyl ether? - Correct Answer>>>: all of
the above



Page 2 of 10

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