3- AROMATICS (PHENOLS) Flashcards

1
Q

what is 2,4,-dichloro-phenoxyacetic acid and how is it synthesized

A

it is a plant growth control

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2
Q

what is agent orange and what it is made of?

A

agent orange is a herbicide
50/50 mix of two compounds:

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3
Q

what is the danger of 2,4,5-T?

A

self reaction can create dioxin, one of the most toxic man made chemicals
even though it is in very small quantities (Cl is not a strong EWG for an aromatic substitution) but it can still happen and it can be very dangerous

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4
Q

what is the LD50?

A

median lethal dose of a toxic substance or radiation (LD50) is the dose to kill half the members of a tested population

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5
Q

what is the structure of bisphenol?

A
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6
Q

how can bisphenol be used to make epoxy resin (glue)?

A

continues to form a polymer

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7
Q

what are applications of epoxy resins?

A

protecting coats in electronic circuit boards
adhesives (glues)
patching holes in concrete pavement

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8
Q

how is synthesis of bisphenol A made from phenol?

A
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9
Q

what is bakelite plastic made from?

A

phenol and formaldehyde

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10
Q

why are benzene reactions different from alkene reactions?

A

benzenes prefer substitution reactions instead of addition reactions
a catalyst and often heat is also often needed for benzene to react

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11
Q

reminder of the directionality of groups on benzene

A
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12
Q

how does BHT prevent food from spoling?

A

breaks the chain reactions that spoil food by scavenging peroxy radicals
peroxy radicals are the things that cause food spoilage

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13
Q

what is needed to make epoxy resin?

A
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14
Q

what is the reaction to make the first polymer part of epoxy resin?

A
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15
Q

what happens when you mix that polymer with the diamine?

A
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16
Q

mechanism for synthesis of bisphenol A

A

when you have phenol type thing, you usually get an attack from the para position, then you have water leaving, carbocation, rearomatization etc

17
Q

synthesis of bakelite

A
18
Q

how does the solvent change the bromination of phenol?

A
19
Q

how is BHT made from 4-methylphenol?

A
20
Q

why does phenol not undergo O-alkylation?

A

because a C-O bond is less stable than a C-C bond

21
Q

how does BHT consume peroxy radicals?

A