Carboxyllic Acids And Derivatives Flashcards
7 ways of making a carboxylic acid
Oxidation of aldehyde
Oxidation of primary alcohol
Hydrolysis of nitrile
Hydrolysis of amide
Grignards reagent
Hydrolysis of ester
Iodoform reaction
Conditions and reagents to oxidise an aldehyde into carboxylic acid
K2cr2o7 and h2so4
Heat
Conditions and reagents for oxidation of alcohol into carboxylic acid
K2cr2o7 and h2so4
Heat under reflux
Conditions and reagents for hydrolysis of nitrile into carboxylic acid
Hcl water and nitrile
Heat under reflux
Conditions and reagents for hydrolysis of amide into carboxylic acid
Water hcl
Heat under reflux
Conditions and reagents for grignards reagents to carboxylic acid
Co2 and grignards
Dry ether acid and water
How to reduce carboxylic acid to alcohol
Lialh4
Dry ether
What are salts formed from carboxylic acids known as
Carboxylates
Why are carboxylic acids acidic but alcohols not
Ion formed in alcohols is less stable as charge can’t be delocalised or shared between 2 oxygen atoms but in carboxylic acids they can be so h+ ions are produced
How to make an acid chloride from carboxylic acid
Add pcl5
Why are acid chlorides so reactive
C delta plus atom which is attacked by nucleotide is in a planar environment so is more accessible
2 electronegative atoms bonded to c atom drawing electrons away from c-cl bond weakening it
Acid chloride reaction adding water
Room temp
Carboxylic acid
Acid chloride plus alcohol
Ester
Room temp
Acid chloride can plus ammonia
Room temp
Amide
Acid chloride plus amine
Room temp
Nitrogen substituted amine