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Flashcards in Mechanisms Deck (62):
1

SN2

2

SN1

3

E2

4

E1

5

Williamson ether synthesis

6

Epoxide formation via halohydrin

7

Dehydration of alcohols with acid

8

Conversion of alcohol to alkyl halide with HX

9

Conversion of alcohol to an alkyl bromide with PBr3

10

Conversion of alcohol to an alkyl chloride with SOCl2

11

Conversion of alcohol to a tosylate with tosyl chloride

12

Epoxide opening with strong nucleophile

13

Epoxide opening with acid and weak nucleophile

14

Electrophilic addition of HX

15

Hydration of Alkenes

16

Electrophilic addition of X2

17

Halohydrin formation

18

Hydroboration-oxidation of alkenes

19

Xoymercuration-demercuration of alkenes

20

Epoxidation using peroxy acids

21

Tans dihydroxylation

22

Oxidative cleavage of alkenes (ozonolysis)

23

Oxidative cleavage of alkenes with oxidative workup (ozonolysis)

24

SN2 substitution with acetylide anion

25

Epoxide opening with acetylide anion

26

Reduction of alkyne to trans alkene

27

Radical bromination of alkenes

28

Radical allylic bromination of alkenes

29

Radical addition of HBr

30

Addition of HX to conjugated dienes (thermodynamic)

31

Addition of HX to conjugated dienes (kinetic)

32

SN2

33

SN1

34

E2

35

E1

36

Williamson ether synthesis

37

Epoxide formation via halohydrin

38

Dehydration of alcohols with acid

39

Conversion of alcohol to alkyl halide with HX

40

Conversion of alcohol to an alkyl bromide with PBr3

41

Conversion of alcohol to an alkyl chloride with SOCl2

42

Conversion of alcohol to a tosylate with tosyl chloride

43

Epoxide opening with strong nucleophile

44

Epoxide opening with acid and weak nucleophile

45

Electrophilic addition of HX

46

Hydration of Alkenes

47

Electrophilic addition of X2

48

Halohydrin formation

49

Hydroboration-oxidation of alkenes

50

Xoymercuration-demercuration of alkenes

51

Epoxidation using peroxy acids

52

Tans dihydroxylation

53

Oxidative cleavage of alkenes (ozonolysis)

54

Oxidative cleavage of alkenes with oxidative workup (ozonolysis)

55

SN2 substitution with acetylide anion

56

Epoxide opening with acetylide anion

57

Reduction of alkyne to trans alkene

58

Radical bromination of alkenes

59

Radical allylic bromination of alkenes

60

Radical addition of HBr

61

Addition of HX to conjugated dienes (thermodynamic)

62

Addition of HX to conjugated dienes (kinetic)