KA3- Oxidation And The Chemistry Of Cooking Flashcards
Alcohols
Compounds that contain hydroxyl functional group -OH (so hydrogen bond)
CnH2n+1O/OH
Higher boiling points than alkanes because hydrogen bonds stronger
Soluble in water because contain polar hydroxyl group
Naming alcohols
Numbering from one side which gives the -OH the lowest number
Ensuring the -OH takes priority over any branches
Primary alcohol
OH group joined to the end of the carbon chain
-CH2OH
Secondary alcohols
OH group joined to an intermediate carbon atom
—CH—
|
OH
Tertiary alcohol
OH group joined to an intermediate carbon atom wich also has a branch attached
|
—C—
|
OH
Propane (alcohols)
Doesn’t have a hydroxyl group so cant from a hydrogen bond with other propane molecules
Much lower boiling point than other molecules as only weak London dispersion force have to be broken to change propane from a liquid to a gas
Adding hydroxyl groups (alcohols)
Molecules are held together by hydrogen bonding in the solid and liquid state
Much more energy must be supplied to overcome the hydrogen bonds which attract the molecules
Oxidation of alcohols
Primary and secondary alcohols can be oxidised by various oxidising agents
Tertiary alcohols don’t undergo oxidisation
Suitable oxidising agents (alcohols)
Acidified potassium dichromate
Hot copper (II) oxide
Primary alcohols oxidised
Produce aldehydes
Primary alcohol—> aldehyde—> carboxylic acid
O:H ratio can help
2/3 H- aldehyde
1/3 H- carboxylic acid
Secondary alcohols oxidised
Produce ketones
Secondary alcohol—> ketone (not readily oxidised)
Aldehydes and ketones
C=O (carbonyl group)
Aldehydes
The carbonyl group is at the end of the carbon chain and has a hydrogen atom attached to it
Prefixal (propanal)
Ketones
Carbonyl group is joined to 2 other carbon atoms and does not have a hydrogen atom attached to it
Prefixone (propanone)
Branched ketones
Position of carbonyl group changes
Position of branches-prefix of how many branches branch name chain prefix-position of carbonyl-one