Back to marketplace

Aromatic Hydrocarbons PPT

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

is the generic term for an aromatic hydrocarbon

Back (Answer)

Arene

#2
Front (Question)

is derived by removal of a hydrogen

Back (Answer)

Aryl group

#3
Front (Question)

Aromatic compounds undergo what kind of reaction

Back (Answer)

Electrophilic Aromatic Substitution

#4
Front (Question)

draw the halogenation reaction and its reactants

Back (Answer)

grade yourself accordingly

#5
Front (Question)

draw the nitration reaction and its reactans

Back (Answer)

grade yourself accordingly

#6
Front (Question)

has a full or positive charge

Back (Answer)

electrophile

#7
Front (Question)

draw the sulfonation reaction and its needed reactants

Back (Answer)

Aromatic compounds undergo

#8
Front (Question)

draw the friedel crafts alkylation

Back (Answer)

grade yourself accordingly

#9
Front (Question)

draw the friedel crafts acylation

Back (Answer)

grade yourself accordingly

#10
Front (Question)

In step 1 of the mechanism, the electrophile reacts with two p electrons from the aromatic ring to form a what

Back (Answer)

arenium ion

#11
Front (Question)

In step 2, a wha is removed and the aromatic system is regenerated

Back (Answer)

proton

#12
Front (Question)

generation of arenium ion is what kind of rxn

Back (Answer)

endothermic

#13
Front (Question)

The first step requires the loss of aromaticity of the very stable benzene ring, which is highly unfavorable thus the first step is rate ____

Back (Answer)

determining

#14
Front (Question)

second step wherein the ring gains it aromatic substitution is highly

Back (Answer)

exothermic

#15
Front (Question)

which has a larger DG‡, first or second step

Back (Answer)

first step

#16
Front (Question)

The ring regains its aromatic stabilization, a highly favorable/unfavorable process

Back (Answer)

favorable

#17
Front (Question)

Halogenation of benzene requires the presence of a what

Back (Answer)

Lewis acid

#18
Front (Question)

A special apparatus is used to perform this reaction

Back (Answer)

fluorination

#19
Front (Question)

occurs so rapidly it is hard to stop at monofluorination of the ring

Back (Answer)

fluorination

#20
Front (Question)

is so unreactive that an alternative method must be used

Back (Answer)

iodine

#21
Front (Question)

draw the iodination reaction

Back (Answer)

grade yourself accordingly

#22
Front (Question)

in nitration, the nitric acid can dissociate to form a what

Back (Answer)

nitronium ion

#23
Front (Question)

is the actual electrophile in nitration; it reacts with benzene to form a resonance-stabilized arenium ion

Back (Answer)

nitronium ion

#24
Front (Question)

Sulfonation occurs most rapidly using what

Back (Answer)

fuming sulfuric acid