Which of the following is false for aromatic compounds? They are unusually stable, and have low heats of hydrogenation They readily undergo substitution reactions There are 4n+2 electrons in a delocalized T-bonding system They readily undergo electrophilic addition reactions

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Which of the following is false for aromatic compounds?
They are unusually stable, and have low heats of hydrogenation
OThey readily undergo substitution reactions
There are 4n+2 electrons in a delocalized T bonding system
They readily undergo electrophilic addition reactions
Transcribed Image Text:Which of the following is false for aromatic compounds? They are unusually stable, and have low heats of hydrogenation OThey readily undergo substitution reactions There are 4n+2 electrons in a delocalized T bonding system They readily undergo electrophilic addition reactions
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Step 1

Aromatic compounds 

Aromatic compounds are chemical compounds that consist of conjugated planar ring systems accompanied by delocalized pi-electron clouds in place of individual alternating double and single bonds.

Or

Aromatic hydrocarbon, are hydrocarbons containing sigma bonds and delocalized pi electrons between carbon atoms in a ring. For e.g. benzene.

They are known as aromatic due to their pleasant smell.

Electrophilic substitution reactions are chemical reactions in which an electrophile displaces a group in a compound, typically but not always hydrogen.

Nucleophilic substitution reactions are those reactions in which substitution is brought about by a nucleophile.

These reactions are denoted by SN1 or SN2 ( S stands for substitution and N for nucleophile).

One of the most common examples of this type of reaction is the hydrolysis of an alkyl halide by aqueous to give alcohols.

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