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43 notecards = 11 pages (4 cards per page)

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Benzene Reactions Test #2

front 1

back 1

Reduction of benzene

front 2

back 2

Reduction of benzene

front 3

back 3

Birch Reduction (reagents can also be called Birch Conditions)

front 4

back 4

Sulfonation of benzene

front 5

back 5

Reverse Sulfonation of benzene

front 6

back 6

Nitration of benzene

front 7

back 7

nitro group reduced to an amine

nitrobenzene to aniline

front 8

back 8

preparing an aniline from benzene

front 9

back 9

Friedel-Crafts Acylation

front 10

back 10

Clemmensen Reduction

front 11

back 11

Friedel-Crafts Alkylation

front 12

back 12

Strong Activators, Ortho/Para Directors

front 13

back 13

Moderate Activators, Ortho/Para Directors

front 14

back 14

Weak activators, Ortho/Para Directors

front 15

back 15

Weak Deactivators, Ortho/Para Directors

front 16

back 16

Strong Deactivators, Meta Directors

front 17

Benzene Nomenclature

back 17

Toluene

front 18

Benzene Nomenclature

back 18

Phenol

front 19

Benzene Nomenclature

back 19

Anisole

front 20

Benzene Nomenclature

back 20

Aniline

front 21

Benzene Nomenclature

back 21

Benzoic Acid

front 22

Benzene Nomenclature

back 22

Benzaldehyde

front 23

Benzene Nomenclature

back 23

Acetophenone

front 24

Benzene Nomenclature

back 24

Styrene

front 25

Benzene Nomenclature

back 25

Chlorobenzene

front 26

Benzene Nomenclature

back 26

Nitrobenzene

front 27

Benzene Nomenclature

back 27

Ethylbenzene

front 28

back 28

Alkylbenzenes oxidized by chromic acid to yield benzoic acid AS LONG AS one benzylic hydrogen is present

front 29

back 29

will work AS LONG AS one benzylic hydrogen is present

front 30

back 30

Cumulated Diene

front 31

back 31

Conjugated Diene

front 32

back 32

Isolated Diene

front 33

back 33

Halogenation of Benzene

front 34

back 34

Aryl diazonium salt to fluorine

front 35

back 35

diazonium salt to hydrogen

front 36

back 36

aryl diazonium salt to hydroxyl group

front 37

back 37

aryl diazonium salt to iodine

front 38

back 38

aryl diazonium salt to nitrile group

front 39

back 39

aryl diazonium salt to bromine

front 40

back 40

aryl diazonium salt to chlorine

front 41

back 41

Leave in group MUST be ortho or para to electron withdrawing group to form the phenol

front 42

back 42

creates diazonium salt

front 43

back 43

cyano group hydrolyzed to carboxylic acid