Chapter 17 Flashcards

0
Q

Bro inaction of a benzene includes

A

Aluminum bromide AlBr2
Or Farers bromide FeBr2
And
Br2

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1
Q

Addition to a benzene ring always consists of

A

A strong nucleophile and a benzene ring

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2
Q

What molecule must be used when Iodinating benzene

A

Nitric acid. HNO3

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3
Q

In what reaction does sulfuric and nitric acid make a nironium catin that ads to a benzene

A

Nitration of benzene

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4
Q

Sulfonate on of benzene ads what group to benzene

A

HSO3 cation

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5
Q

What are the reactants to sulfonate a benzene

A

Concentrated sulfuric acid ( fuming ) H2SO4
Sulfur trioxide (SO3)
Benzene

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6
Q

The main purpose of friedel craft alkylation is to create

A

Alkyl benzenes

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7
Q

Friedel craft acylation creates

A

Acylbenzenes

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8
Q

What is the purpose of the strong Lewis acid in the fridel craft reactions

A

Creates a poor complex with the alkyl halide so the benzene can attack the positive carbon

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9
Q

What are the reactants for a friedel craft alkylation

A

Alkylehalide

Strong lewis acid of the same halide

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10
Q

The only difference between acylation and alkylation of benzene is

A

An acylhalide is used I place of an alkyl halide

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11
Q

When using friedel craft alkylation the a carbocation is created
What will this cause that can change the expected result

A

Rearrangement

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12
Q

Freidel craft reactions will not work if what is already present on the benzene

A

Deactivatiion group stronger than a halogen

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13
Q

A group attached to a benzene that allowed them compound to react faster than benzene by its self is known as an

A

Activating group

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14
Q

A group attached to a benzene that makes the compound react slower than a benzene is known as a

A

Deactivating group

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15
Q

Activating groups will give reactants with what configuration

A

Ortho and para

16
Q

Deactivating groups will give what formation

17
Q

What deactivating group is an exception that will give ortho and para

18
Q

What type of group gives the best resonance structure when attached to the ortho and para

A

Activating

19
Q

What group gives very unstable resonance structures when another group is reacted at the ortho and pare

A

Deactivating

20
Q

When there are two preexisting groups on a benzene what position will a new reactant almost never be placed

A

Ortho between the two preexisting groups

21
Q

Why will a new group not react to the ortho position between two groups

A

Steric hindrance

22
Q

What reaction will reduce acyle benzenes with
Amalgamated zinc ( Zn(Hg))
Aqueous HCl

A

Clemmonsen reduction

23
Q

If a friedel craft alkylation reaction fails to creat a product due to rearrangement what two reactions can be done to reach the wanted product

A

Friedel craft acylation. Then a Clemmenson reduction

24
Clemmenson reductions end product is an
Alkylbenzene
25
Gatterman-Koch formulation produces what end product
Benzaldehyde
26
Gatheran -Koch formulation can be spit into three reactions. What are the reactants and product of the first and second
CO + HCl =. Chloroaldehyde Chloroaldehyde + AlCl3 /Cucl = Carbonyl cation
27
The third part of the Gatterman -Koch reaction is
The addition of the carbonyl cation to the benzene
28
All of the reactants for the Gatterman -Koch reaction can be placed together then added to benzen. What are all the reactants
CO. HCl Aluminum chloride (AlCl3) Copper chloride (CuCl) Benzene
29
Side chain oxidation oxidizes all alkenes to what
Carboxilic acids
30
What groups will not oxidize in side chain oxidation
Nitrite (NO3) SO3H Carboxylic acid
31
What oxidizes can be used for side chain oxidation
KMnO4 , -OH, H2O at 100 C Or Chromic acid (hot)
32
Side chain allegation is what type of reaction
Free radical halogenation
33
Halogens will always go to what carbon in free radical halogenation
Benzilic