Exam 3 Flashcards

(43 cards)

1
Q

what does mCPBA do in a rxn

A

adds Oxygen between double bond like a dart

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2
Q

what does H2SO4 and H2O add in a rxn

A

adds OH and H (H goes to least stable)

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3
Q

what kind of products do H2SO4 and H2O yield in a rxn

A

trans markovnikov

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4
Q

what kind of products to BH3 and H2O2/NaOH yield in a rxn

A

anti-markovnikov

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5
Q

what would it look like if there were two OH groups on neighboring carbons in a ring where OsO4 and NMO are reagents

A

OH are cis

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6
Q

what would it look like if there were two OH groups on neighboring carbons in a ring where mCPBA, H2SO4, H2O are reagents

A

OH are trans

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7
Q

what is initiation

A

no radical to one radical

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8
Q

what is propagation

A

radical moves

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9
Q

what is termination

A

one radical to no radical

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10
Q

what does O3 do

A

breaks double bond in two

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11
Q

what does KMnO4 do

A

acts like O3 but adds alcohol

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12
Q

to add 2 Br to alkene but 4 to alkyne add..

A

Br2

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13
Q

to add 1 Br to alkene but 2 to alkyne add..

A

HBr

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14
Q

what does OsO4 do

A

turns to single bond

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15
Q

what does NaIO4 do

A

splits carbon bond

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16
Q

explain how acidic rxn occurs

A

e- from O move to make double bond, e- from double bond move to break bond and go to H+, then e- from bond go to oxygen to neutralize and H+ goes to H2O to yield ketone and H3O+

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17
Q

what yields when Lindlar’s catalyst is used

A

cis alkene from alkyne

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18
Q

what yields when Li, NH3 used

A

trans alkene from alkyne

19
Q

what kind of reaction occurs with KOtBu

20
Q

what are base molecules we might see

21
Q

what are molecules that are both basic and nucleophilic

22
Q

what are nucleophilic molecules we might see

A

NaCN, NaN3, NaOAc

23
Q

what reactions will never be elimination

24
Q

when there is a base and nucleophile, what reaction will CH3X yield

25
when there is a base only, what reaction will CH3X yield
Sn2
26
when there is a nucleophile only, what reaction will CH3X yield
Sn2
27
when there is neither a base or nucleophile, what reaction will CH3X yield
none
28
when there is a base and nucleophile, what reaction will a primary carbon yield
Sn2/E2
29
when there is a base and nucleophile, what reaction will a secondary carbon yield
Sn2/E2
30
when there is a base and nucleophile, what reaction will a tertiary carbon yield
E2
31
when there is a base only, what reaction will a primary carbon yield
E2
32
when there is a base only, what reaction will a secondary carbon yield
E2
33
when there is a base only, what reaction will a tertiary carbon yield
E2
34
when there is a nucleophile only, what reaction will a primary carbon yield
Sn2
35
when there is a nucleophile only, what reaction will a secondary carbon yield
Sn2
36
when there is a nucleophile only, what reaction will a tertiary carbon yield
none
37
when there is neither a base or nucleophile, what reaction will a primary carbon yield
none
38
when there is neither a base or nucleophile, what reaction will a secondary carbon yield
Sn1/E1
39
when there is neither a base or nucleophile, what reaction will a tertiary carbon yield
Sn1/E1
40
what does POCl3, pyr do
talkes alcs to alkenes in E2 rxn
41
what does PBr3 do
takes alcs to Br in Sn2
42
what does SOCl2 do
takes alcs to Cl in Sn2
43
what does adding NaNH2/NaNH3 do? how do you treat?
adds carbon ... treat with carbon group and chloride