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Chemistry
Organic
Alcohols
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Alcohols can be
dehydrated
to form alkenes
alkenes
can be hydrated to form alcohols
alcohols undergo
elimination
reactions with a
concentrated
acid catalyst to produce
alkenes
alkenes can be heated with
steam
in the presence of an acid
catalyst
to produce
alcohols
Hydroxyls have
two
lone pairs of electrons
Hydrating
an alkene is the standard industrial method for producing
alcohols
Conditions for fermentation
yeast
30-40
degrees
anaerobic
conditions
Hydration of an alkene produces a
pure alcohol
whereas fermentation is very
impure
Fermentation is more
sustainable
than hydrating alkenes as glucose is a
renewable
resource whereas alkenes come from
crude oil
biofuels are fuels made from
biological material
biofuels are considered carbon
neutral
as they release the same amount of
carbon dioxide
as the plant took in when it was growing
disadvantages of biofuels
land cannot be used to grow
crops
deforestation
to make land
fertilisers
can pollute water
primary alcohols are oxidised to
aldehydes
, then to
carboxylic acids
secondary alcohols are oxidised to
ketones
tertiay alcohols are not
oxidised
aldehydes and ketones are
carbonyl
compunds as they contain the functional group
C=O
the notation [O] represents an
oxidising
agent
primary alcohols are gently
oxidised
by
distillation
to form
aldehydes
primary alcohols are vigorously oxidised by
reflux
to form
carboxylic acids
to form carboxylic acids the primary alcohol has to by
heated
with
excess oxidising
agent
heating under reflux means the temperature can be
increased
to boiling without losing
volatile
solvents,
reactants
or
products
secondary alcohols are
oxidised
by reflux in acidic conditions to form
ketones
Fehling’s solution and Benedict’s solution
aldehyde
= brick red
ketone
= stays blue
Tollens‘ solutions
aldehyde =
silver mirror
ketone =
clear
The oxidising agent used to oxidise alcohols is
acidified
potassium
dichromate
Acidified potassium dichromate changes from
orange
to
green
when an alcohol is oxidised