Ch 18-19 Rxns

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Last updated 4:44 AM on 2/6/26
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105 Terms

1
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<p>Product?</p>

Product?

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2
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<p>Reagents?</p>

Reagents?

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3
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<p>directing group?</p>

directing group?

ortho/para director, weakly deactivating

4
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<p>mechanism?</p>

mechanism?

EAS

5
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<p>Conditions/Notes</p>

Conditions/Notes

Phenols and anisoles over-halogenate

6
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<p>Product?</p>

Product?

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7
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<p>Reagents?</p>

Reagents?

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8
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<p>Directing group?</p>

Directing group?

meta director, strongly deactivating

9
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<p>Mechanism?</p>

Mechanism?

EAS

10
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<p>Notes/Conditions?</p>

Notes/Conditions?

Aniline cannot be nitrated

11
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<p>Product?</p>

Product?

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12
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<p>Reagents?</p>

Reagents?

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13
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<p>Directing group?</p>

Directing group?

Meta director, strong deactivating

14
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<p>Mechanism?</p>

Mechanism?

EAS

15
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<p>Conditions?</p>

Conditions?

Only adds para when added to a ring with an ortho/para director

16
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<p>Product?</p>

Product?

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17
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<p>Reagents?</p>

Reagents?

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18
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<p>Directing group?</p>

Directing group?

meta director, moderately deactivating

19
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<p>Mechanism? </p>

Mechanism?

EAS

20
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<p>Conditions/Notes</p>

Conditions/Notes

Friedel-Crafts Acylation cannot occur with a meta director or NH2 on the ring

21
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<p>Product?</p>

Product?

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22
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<p>Reagents?</p>

Reagents?

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23
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<p>Directing Group</p>

Directing Group

Ortho/para director, weakly activating

24
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<p>Mechanism?</p>

Mechanism?

EAS with carbocation rearrangements

25
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<p>Conditions/Notes</p>

Conditions/Notes

Friedel-Crafts alkylation, cannot occur with a meta director or NH2 on the ring, benzene rings must be in excess

26
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<p>Product?</p>

Product?

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27
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<p>Reagents?</p>

Reagents?

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28
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<p>Directing group?</p>

Directing group?

Ortho/para director, weakly activating

29
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<p>Mechanism?</p>

Mechanism?

EAS with carbocation rearrangements

30
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<p>Conditions/Notes</p>

Conditions/Notes

Friedel-Crafts alkylation without a catalyst cannot occurs with a meta director or NH2 on a ring, benzene rings must be in excess

31
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<p>Products?</p>

Products?

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32
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<p>Reagents?</p>

Reagents?

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33
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<p>Mechanism?</p>

Mechanism?

NAS

34
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<p>Conditions/Notes?</p>

Conditions/Notes?

Nu is often -OR or -NH2, requires a NO2 or a carbonyl ortho or para to the good leaving group (a halide)

35
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<p>Products?</p>

Products?

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36
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<p>Reagents?</p>

Reagents?

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37
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<p>Mechanism?</p>

Mechanism?

Reduction

38
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<p>Reaction name?</p>

Reaction name?

Wolff-Kishner Reduction

39
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<p>Product?</p>

Product?

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40
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<p>Reagents?</p>

Reagents?

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41
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<p>Mechanism?</p>

Mechanism?

Reduction

42
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<p>Reaction Name?</p>

Reaction Name?

Clemmensen Reduction

43
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<p>Product?</p>

Product?

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44
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<p>Reagents?</p>

Reagents?

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45
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<p>Mechanism?</p>

Mechanism?

Reduction

46
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<p>Notes</p>

Notes

Also reduces nonaromatic pi bonds

47
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<p>Products?</p>

Products?

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48
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<p>Reagents?</p>

Reagents?

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49
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<p>Mechanism?</p>

Mechanism?

Reduction

50
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<p>Notes?</p>

Notes?

Special for nitriles

51
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<p>Products?</p>

Products?

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52
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<p>Reagents?</p>

Reagents?

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53
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<p>Mechanism?</p>

Mechanism?

Organometallic Reactions

54
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<p>Rxn Name?</p>

Rxn Name?

Suzuki Rxn

55
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<p>Products?</p>

Products?

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56
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<p>Reagents?</p>

Reagents?

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57
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<p>Mechanism?</p>

Mechanism?

Organometallic Reaction

58
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<p>Rxn name?</p>

Rxn name?

Gilman reagents/organocuprates

59
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<p>Products?</p>

Products?

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60
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<p>Reagents?</p>

Reagents?

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61
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<p>Products?</p>

Products?

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62
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<p>Mechanism?</p>

Mechanism?

Radical Reactions

63
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<p>Products?</p>

Products?

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64
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<p>Reagents?</p>

Reagents?

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65
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<p>Mechanism?</p>

Mechanism?

Substitution or Elimination

66
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<p>Conditions?</p>

Conditions?

Mechanism depends on conditions

67
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<p>Products?</p>

Products?

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68
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<p>Reagents?</p>

Reagents?

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69
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<p>Mechanism?</p>

Mechanism?

Elimination, E2 (Hoffman)

70
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<p>Products?</p>

Products?

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71
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<p>Reagents?</p>

Reagents?

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72
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<p>Mechanism?</p>

Mechanism?

oxidation of alkyl side chains

73
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<p>Conditions/Notes</p>

Conditions/Notes

Requires a benzylic hydrogen (not quaternary Carbon)

74
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<p>Reagents?</p>

Reagents?

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75
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<p>Products?</p>

Products?

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76
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<p>Notes/Conditions?</p>

Notes/Conditions?

Formation of diazonium salts from aniline

77
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<p>Products?</p>

Products?

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78
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<p>Reagents?</p>

Reagents?

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79
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<p>Notes?</p>

Notes?

Replacement of a diazonium salt with Cl

80
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<p>Products?</p>

Products?

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81
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<p>Reagents?</p>

Reagents?

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82
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<p>Notes?</p>

Notes?

Replacement of a diazonium salt with Br

83
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<p>Products? </p>

Products?

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84
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<p>Reagents?</p>

Reagents?

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85
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<p>Notes?</p>

Notes?

Replacement of a diazonium salt with CN

86
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<p>Reagents?</p>

Reagents?

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87
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<p>Products?</p>

Products?

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88
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<p>Notes?</p>

Notes?

Replaces diazonium salt with I

89
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<p>Products?</p>

Products?

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90
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<p>Reagents?</p>

Reagents?

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91
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<p>Notes?</p>

Notes?

Replaces a diazonium salt with F

92
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<p>Products?</p>

Products?

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93
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<p>Reagents?</p>

Reagents?

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94
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term image

Replacement of a diazonium salt with OH

95
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<p>Products?</p>

Products?

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96
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<p>Reagents?</p>

Reagents?

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97
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term image

Replacement of a diazonium salt with H, โ€œremovalโ€ of the group from benzene

98
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<p>Reagent?</p>

Reagent?

Any EAS mechanism

99
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<p>Product?</p>

Product?

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100
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<p>Directing group?</p>

Directing group?

Follow the chart