3.2.3 Synthesis of CFCs Flashcards
Photochemical reactions
Reactions started by UV light
Free radical substitution
Cl or Br replaces Hydrogen atom
Free radical
Particles with an unpaired electron
How are free radicals formed
A covalent bond splits equally and one electron goes to each species
Free radicals
reactivity
reason
very reactive
unpaired electron
Stages in synthesis of a chloroalkane
3
initiation
propagation
termination
Initiation stage
(photo dissociation)
free radicals are produced
sunlight provides energy for this to happen
UV present
Propagation stage
(chain reaction)
free radicals used up and created
continues until all Cl2 or CH4 used up
Substitutions
middle step
chlorine in excess = hydrogen atoms replaced by chlorine
methane in excess = chlorine used up quickly
Termination stage
(free radicals used up)
2 free radicals form a covalent bond which makes it a stable molecule
CFCs
chlorofluorocarbons
all hydrogen atoms replaced by chlorine and fluorine atoms
Ozone
O3
The ozone layer
in the upper atmosphere, absorbs UV light from sun
Which bonds in CFCs break in ozone
how
c-cl
broken by UV
free radical catalysts
Safer alternative to CFCs
HFCs