3.2.3 Synthesis of CFCs Flashcards

1
Q

Photochemical reactions

A

Reactions started by UV light

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2
Q

Free radical substitution

A

Cl or Br replaces Hydrogen atom

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3
Q

Free radical

A

Particles with an unpaired electron

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4
Q

How are free radicals formed

A

A covalent bond splits equally and one electron goes to each species

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5
Q

Free radicals
reactivity
reason

A

very reactive

unpaired electron

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6
Q

Stages in synthesis of a chloroalkane

3

A

initiation
propagation
termination

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7
Q

Initiation stage

A

(photo dissociation)
free radicals are produced
sunlight provides energy for this to happen
UV present

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8
Q

Propagation stage

A

(chain reaction)
free radicals used up and created
continues until all Cl2 or CH4 used up

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9
Q

Substitutions

middle step

A

chlorine in excess = hydrogen atoms replaced by chlorine

methane in excess = chlorine used up quickly

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10
Q

Termination stage

A

(free radicals used up)

2 free radicals form a covalent bond which makes it a stable molecule

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11
Q

CFCs

A

chlorofluorocarbons

all hydrogen atoms replaced by chlorine and fluorine atoms

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12
Q

Ozone

A

O3

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13
Q

The ozone layer

A

in the upper atmosphere, absorbs UV light from sun

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14
Q

Which bonds in CFCs break in ozone

how

A

c-cl
broken by UV
free radical catalysts

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15
Q

Safer alternative to CFCs

A

HFCs

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16
Q

CFCs
properties
3

A

unreactive
non-toxic
non-flammable

17
Q

CFCs

cause

A

damage to the ozone layer

18
Q

CFCs
used in
4

A

aerosols
foams
refrigerants
solvents