p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.

p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if
applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.
SO3
H2SO4
Modify the starting material to draw the major product.
Select
Draw
Rings
More
CH 0 S F
Erase

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