alcohols have relatively low volatility due to
their ability to form hydrogen bond between alcohol molecules.
The longer the hydrocarbon chain (solubility)
the less soluble the alcohol.
uses of alcohols: methanol and ethanol
ethanol: alcohol in drinks, solvent in methylated spirits
methanol: petrol additive to improve combustion, feedstock
primary alcohol
one carbon is attached to carbon adjoining the oxygen
secondary alcohol
two carbons are attached to carbon adjoining the oxygen
tertiary alcohol
three carbons are attached to carbon adjoining the oxygen
complete combustion products and equation
products: co2 and h2o
equation: alcohol + o2 -> co2 + h2o
what is the typical oxidising agent for alcohols
potassium dichromate (k2cr2o7_
partial oxidisation of primary aldehyde
primary alcohol-> aldehyde
potassium dichromate and dilute sulfuric acid
warm gently and distil
aldehyde ending and bond
-al
c=o c-h
-CHO
full oxidation of primary carboxylic acid
primary alcohol-> carboxylic acid
excess acidified potassium dichromate
heat under reflux
carboxylic ending
anoic acid
cooh
oxidation of secondary ketone
secondary alcohol-> ketone
acidified potassium dichromate
heat under reflux
ketone ending-
-one
colour change for potassium dichromate
orange dichromate ion ( cr2o7-) reduces to green cr3+ ion
when ketones have 5+ carbons
number is needed to show position
dehydration reactions
removal of a water molecule from a molecule
substitution reaction: alcohol to haloalkanes with
concentrated sulfuric acid and sodium halide