midterm 1 Flashcards

1
Q

conditions for allylic bromination

A

NBS, ccl4, heat light or peroxide

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2
Q

conditions for halogenation of benzene? ex cl2 or br2

A

for cl2 you need cl2 and fecl3. for br2 you need br2 and febr3

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3
Q

what do you need for nitration and what temp

A

hno3, h2so4, 50 degrees

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4
Q

what do you need for sulfonation

A

concentrated h2so4

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5
Q

what do you use for desulfonation?

A

dilute h2so4 (more water, equilibrium to the left)

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6
Q

what do you need for friedel crafts alkylation

A

alcl3

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7
Q

what do you need for friedel crafts acylation?

A

excess benzene, alcl3

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8
Q

what is friedel crafts not good for? and how do we fix it

A

not good for making straight alkylbenzene. do an acylation and then clemmensen or wolff-kishner to reduce ketone to give unbranched alkylbenzene

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9
Q

what do you need for clemmensen reduction?

A

zn(hg), hcl and reflux

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10
Q

what do you need for wolff kishner reduction?

A

nh2nh2, koh, heat

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11
Q

what do you need for benzylic halogenation?

A

halogen, heat or light

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12
Q

how to turn alkylbenzene into benzoic acid?

A

add kmno4, ho-, light. cuts at the benzylic h

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13
Q

what do you need for birch reduction?

A

na, liquid nh3, etoh

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14
Q

at lower temp what is the product?

A

kinetic product (formed faster)

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15
Q

at higher temp what is the product?

A

thermodynamic product (more stable)

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16
Q

equation for huckles rule

A

4n+2

17
Q

what happens when you use a cyclic anhydride in an acylation?

A

new ring is added

18
Q

how do you convert toluene to benzoic acid

A

kmno4/ho- and light

19
Q

converting double and triple bonds to alcohol

A

add bh3, then h2o2 with ho-

20
Q

how to make a double bond into a cyclic oxide thing

A

add peroxide

21
Q

dihydroxylation of alkenes

A

kmno4, cold oh

22
Q

what do you need to break a double bond with h2?

A

catalyst