17.3 2 Preparations and reactions of carboxylic acids Flashcards
How are carboxylic acids formed
Oxidation of primary alcohol or aldehyde oxidising agent of acidified potassium dischromate heat mixture under reflux
when oxidation is complete reaction is fractionally distilled to obtain a pure sample of carboxylic acid
Preparation by hydrolysis
Nitrites are organic molecules containing the CN
Hydrolysed by heating under reflux with either a dilute acid or aqueous alkali
the same apparatus of preparation and purification
C triple N bond breaks
acidic hydrolysis
get NH4+ also forming-see equations in the book
alkaline hydrolysis
NH3 AND get salt ion that if add dilute acid will form carboxylic acid
Reduction
Can be reduced to primary alcohols but not aldehydes this is because aldehydes are more easily reduced than carboxylic acids so an aldehydes formed would be immediately reduced to a primary alcohol
Use lithium tetrahydrioaluminate
solvent of dry ether
formation of water
Neutralisation
mix with aqueous alkali carboxylate salts RCOONa sodium ethanoate used in hand warmers and salt and vingar crips are ionic the salts
Halogenation
OH replaced by halogen atom functional group becomes COCl acyl chlorides that are highly reactive reagent is phosphorus (V) chloride anhydrous conditions reagent+ acyl chloride react with water reaction is vigrous no heating required see equation in book
Acyl chlorides
named using -oyl chloride RCOCl
Halogenation inorganic products
phosphorus trichloride oxide mixes with the acyl chloride has to be separated by fractional distillation
Hydrogen chloride gas escapes as misty fumes
Esterification
carboxylic acid is mixed with an alcohol and small amount of acid catalyst often concentrated sulphuric
acid
even though use a catalyst the reaction is still slow and reversible
Where are esters found
Used in industry as solvents and making polymers (polyesters) . Common in nature responsible for smell of fruits and many animal fats and vegetable oils are esters