Final review Flashcards

1
Q

addition of OH and Br to (alkene to alkane)

A

Br2+ H20

Br attaches and makes a triangle, h20 attacks from the other side and opens up triangle

maokovnikov addition of OH

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2
Q

maokovnikov addition of OH to alkene

A

Oxymerc/demurc

Hg(OAC)2, H20
NaBH4, OH-

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3
Q

anti addition of OH to alkene

A

Bh3, THF

H202,h20, NaOh

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4
Q

mcpba forms a ___ on a _____

it attacks the_____

A

forms a triangle bond of O

on an alkene

it attacks the richest pi bond (the one with more activating groups attached)

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5
Q

syn addition of two Oh’s on (alkene–>alkane)

A

vicinal diol sythesis

OSO4,THF
H2s

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6
Q

antimarkovnikov addition of Br (alkene to alkane)

A

HBr and ROOR (peroxide)

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7
Q

Internal alkyne synthesis (alkane to alkyne)

A

2NaNH2

NH3 (l)

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8
Q

terminal alkyne synthesis (alkane to alkyne)

A

3NaNH2

NH3(l)

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9
Q

addition of Br(s) to terminal alkyne

A

H-Br

adds markovnikovly

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10
Q

addition of halogen to internal alkynes

A

Br2

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11
Q

markovnkov addition of =O (alkyne to alkane)

A

H20, H2SO4

first adds OH (enol) then touts to ketone

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12
Q

alkyne to alkane

A

H2, PD

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13
Q

alkyne to alkene

A

H2 and Lndlards

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14
Q

E alkene synthesis

anti addition of H’s (alkyne to alkene

A

Na

Nh3

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15
Q

antimarkovnikov addition of =O (alkyne to alkene)

A

BH3,THF
H202,OH-

if Borane is big it doesn’t add c=o

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16
Q

ozonolysis of an alkene can make?

A

aldehydes and ketones

reagents: 03, (Ch3)2S

17
Q

addition of Br to allylic (one carbon away from double bond)

A

NBS CCl4 hv

18
Q

addition of hydrogen and halogen 1,4

A

Hx and high T

19
Q

additionof hydrogen halogen 1,2

A

HX and low T

20
Q

addition of halogens 1,4

A

X2 and high T

21
Q

addition of halogens 1,3

A

x2 and low T

22
Q

conroatory

A

4n with heat

4n+2 with light

23
Q

hydrogenation of benzene

A

H2, catalys

24
Q

addition of halogen to benzene

A

x2, Fex3

25
Q

Nitration of benzene ring

A

HNO3 H2SO4

26
Q

sulfonation of benzene ring

A

SO3 H2SO4

27
Q

activating groups ___ electrons

_____ directing

A

activating groups push electrons towards benzene ring

ortho / para directing

28
Q

NO2 to NH2

A

clemenson’

ZnHG HCL Heat

29
Q

NH2 to NO2

A

CF3CO2h