How Do you make a... Flashcards
Carboxylic acid
Oxidation of primary alcohol
- heat an alcohol under reflux with potassium/sodium dichromate and sulphuric acid
- it will not undergo anymore reaction
Ester
Esterification
- react an alcohol with a carboxylic acid in the presence of an acid catalyst
Aldehyde
Oxidation of primary alcohol
- heat an alcohol with potassium/sodium dichromate and sulphuric acid
- distil immediately to prevent any further reaction
Ketone
Oxidation of an secondary alcohol
- heat an alcohol with potassium/sodium dichromate and sulphuric acid to make a ketone
- it will not undergo anymore reaction
How do you make Alkenes from alkanes
Cracking
How do you make alkanes from alkenes
Hydrogenation
- 150 degrees, nickel catalyst in a reaction chamber
How to make Haloalkanes from alkanes
Radical substitution
- UV light
- Draw radical substitution to form chloromethane
How to make Haloalkanes from alkenes
Halogenation
- add a halogen across a C=C bond the alkene becomes saturated and a dihaloakane is produced, this can be used to test for saturation
- when bromine or iodine is added there is no reaction
polymers from alkenes
Addition polymerisation
- during polymerisation monomers have there pie bond broken and the electrons from each pie bond make and sigma bond with a neighbouring carbon atom
How do you make alcohol from alkenes
Hydration
- gaseous alkene and steam
- phosphoric acid catalyst at 300 degrees and 65 atm
How do you make alkenes from alcohols
Dehydration
- alcohol heated with a strong acid (sulphuric acid) at 170 degrees under reflux
- water is eliminated to make an alkene, the OH group from one carbon atom and H group from another carbon atom are lost to form a water molecule, the pie bond forms between 2 adjacent carbon atoms
How do you make alcohols from haloalkane
Hydrolysis using aqueous alkali
- haloalkane is heated under reflux with an aqueous solution containing hydroxide ions an alcohol is made
Nucleophilic substitution reaction
- water is the reactant that provides the hydroxide ions that act as nucleophiles - if water is used one of the H-O bonds in a molecule undergoes hetrolytic fission to product the nucleophile OH-
- this species attacks the electron deficient carbon atom in the haloalkane molecules then once the nucleophile has bonded to the haloalkane, the C-X bond undergoes hetrolytic fission to produce a halide ion
How do you make haloalkanes from alcohols
Halide Substitution
- Hydrogen halide is the reagent that would be used but the Halide would be the species directly involved in the reaction
- sulphuric acid or a strong acid catalyst is used and the mixture is heated to increased the rate of reaction
- However when iodide is reacted phosphoric acid is used because the sulphuric acid oxidises iodide ions to iodine so the yield of iodoalkane is low