Mechanisms

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112 Terms

1

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<p>Product?</p>

Product?

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2

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<p>Reactant?</p>

Reactant?

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3

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<p>Reagents?</p>

Reagents?

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4

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Mark addition of H and OH (no rearrangement)

<p>Mark addition of H and OH (no rearrangement)</p>

5

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<p>Product?</p>

Product?

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6

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<p>Reactant?</p>

Reactant?

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7

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<p>Reagents?</p>

Reagents?

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8

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Mark addition of H and OR

<p>Mark addition of H and OR</p>

9

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<p>Product?</p>

Product?

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10

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<p>Reactant?</p>

Reactant?

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11

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<p>Reagents?</p>

Reagents?

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12

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Anti mark addition of OH (trans)

13

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<p>Product?</p>

Product?

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14

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<p>Reactant?</p>

Reactant?

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15

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<p>Reagents?</p>

Reagents?

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16

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Anti mark addition of Br

17

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<p>Product?</p>

Product?

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18

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<p>Reactant?</p>

Reactant?

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19

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<p>Reagents?</p>

Reagents?

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20

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Mark addition of Br

21

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<p>Product?</p>

Product?

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22

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<p>Reactant?</p>

Reactant?

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23

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<p>Reagents?</p>

Reagents?

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24

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Addition of Br2 (trans)

25

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<p>Product?</p>

Product?

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26

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<p>Reactant?</p>

Reactant?

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27

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<p>Reagents?</p>

Reagents?

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28

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Oxidation of alkene to an epoxide

29

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<p>Product?</p>

Product?

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30

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<p>Reactant?</p>

Reactant?

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31

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<p>Reagents?</p>

Reagents?

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32

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Anti Mark epoxide ring opening (basic conditions) (trans sides)

33

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<p>Product?</p>

Product?

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34

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<p>Reactant?</p>

Reactant?

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35

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<p>Reagents?</p>

Reagents?

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36

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Mark epoxide ring opening (acidic conditions) (trans sides)

37

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<p>Product?</p>

Product?

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38

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<p>Reactant?</p>

Reactant?

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39

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<p>Reagents?</p>

Reagents?

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40

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Mark addition of Br (less stable C) and OR (more stable C) trans with bromonium bridge forming in between

41

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<p>Product?</p>

Product?

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42

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<p>Reactant?</p>

Reactant?

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43

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<p>Reagents?</p>

Reagents?

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44

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Formation of a cyclopropane

45

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<p>Product?</p>

Product?

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46

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<p>Reactant?</p>

Reactant?

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47

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<p>Reagents?</p>

Reagents?

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48

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Cis addition of 2 H’s

49

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<p>Product?</p>

Product?

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50

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<p>Reactant?</p>

Reactant?

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51

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<p>Reagents?</p>

Reagents?

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52

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Addition of 2 H’s per pi bond

53

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<p>Product?</p>

Product?

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54

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<p>Reactant?</p>

Reactant?

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55

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<p>Reagents?</p>

Reagents?

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56

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Addition of 2 H’s to a pi bond CIS

57

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<p>Product?</p>

Product?

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58

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<p>Reactant?</p>

Reactant?

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59

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<p>Reagents?</p>

Reagents?

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60

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Addition of 2 H’s to a pi bond TRANS

61

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<p>Product?</p>

Product?

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62

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<p>Reactant?</p>

Reactant?

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63

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<p>Reagents?</p>

Reagents?

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64

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

1 degree alcohol to aldehyde

65

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<p>Product?</p>

Product?

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66

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<p>Reactant?</p>

Reactant?

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67

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<p>Reagents?</p>

Reagents?

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68

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

2 degree alcohol to ketone

69

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<p>Product?</p>

Product?

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70

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<p>Reactant?</p>

Reactant?

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71

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<p>Reagents?</p>

Reagents?

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72

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

1 degree alcohol or aldehyde to carboxylic acid

73

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<p>Product?</p>

Product?

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74

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<p>Reactant?</p>

Reactant?

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75

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<p>Reagents?</p>

Reagents?

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76

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Addition of 2 OH groups to a pi bond (CIS)

77

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<p>Product?</p>

Product?

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78

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<p>Reactant?</p>

Reactant?

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79

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<p>Reagents?</p>

Reagents?

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80

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Splitting of pi bond (each replaced with double bond to O)

81

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<p>Product?</p>

Product?

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82

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<p>Reactant?</p>

Reactant?

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83

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<p>Reagents?</p>

Reagents?

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84

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<p>Description of reaction and mechanism</p>

Description of reaction and mechanism

Splitting of pi bond (each replaced with double bond to O) (H becomes an OH)

85

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<p>Product?</p>

Product?

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86

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<p>Reactant?</p>

Reactant?

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87

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<p>Reagents?</p>

Reagents?

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88

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Mark addition of H and X

89

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<p>Product?</p>

Product?

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90

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<p>Reactant?</p>

Reactant?

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91

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<p>Reagents?</p>

Reagents?

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92

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Addition of X2 (trans product)

93

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<p>Product?</p>

Product?

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94

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<p>Reactant?</p>

Reactant?

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95

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<p>Reagents?</p>

Reagents?

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96

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

enol to keto via tautomerization

97

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<p>Product?</p>

Product?

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98

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<p>Reactant?</p>

Reactant?

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99

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<p>Reagents?</p>

Reagents?

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100

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<p>Description of reaction and mechanism </p>

Description of reaction and mechanism

Mark addition of H2O to an alkyne