4.2.1 Alcohols Flashcards
General formula of alcohols
CnH2n+1OH
Two methods to make alcohols
Fermentation or hydration
How to identify 3 types of alcohol
Primary - carbon with OH attached has 1 other C atoms bonded.
Secondary - carbon with OH attached has 2 other C atoms bonded.
Tertiary - carbon with OH attached has 3 other C atoms bonded.
Explanation of solubility
Water soluble as they are polar molecules as there is a large difference in electronegativity between C and O. The lone pair on O can H-bond with the H of a water molecule.
boiling point of alcohols compared to equivalent alkanes
Higher than other organic molecules. The OH functional group is able to H-bond to the OH group on other alcohol molecules. H-bonds are the strongest intermolecular force meaning more energy is needed to overcome them.
Combustion of alcohols
Alcohols make good fuels as lots of energy is released in combustion.
Alcohol + O2 –> CO2 + H2O
What type of reaction occurs between an alcohol and halide ions
nucleophilic substitution
Condition for halogenation of an alcohol
NaX/H2SO4
where X is the halogen
Equation for reaction of ethanol with HBr and conditions
CH3CH2OH + HBr –> CH3CH2Br + H2O
Conditions: NaBr/H2SO4 to produce the HBr
Type of reaction where an alkene is formed from an alcohol
Dehydration or elimination
Conditions for forming an alkene from an alcohol
heat with concentrated phosphoric acid (H3PO40
Primary alcohols are oxidised to form…
aldehydes and/or carboxylic acids
Secondary alcohols are oxidised to form…
ketones
Tertiary alcohols are oxidised to form..
N/A tertiary alcohols cannot easily be oxidised
Conditions for forming an aldehyde from a primary alcohol
heat with acidified potassium dichromate and distil off the product