-OH Flashcards
What are alcohols?
Alcohols are part of the homologous series (-OH).
THEY ARE SATURATED ORGANIC MOLECULES as they contain only single carbon to carbon bonds.
They have a general formula of CnH2n+1OH .
They have a gradation in their physical properties (their boiling points and melting points increase as the chains get larger)
What is the boiling point in degrees Celsius of alcohols from methanol to pentanol?
Methanol: 65 Ethanol: 79 Propanol: 97 Butanol: 117 Pentanol: 138
What are primary alcohols?
When the -OH group is attached to a carbon with no more than 1 alkyl group
What are secondary alcohols?
When the -OH group is attached to a carbon with no more than 2 alkyl groups
What are tertiary alcohols?
When the -OH group is attached to a carbon with no more than 3 alkyl groups
What are the trends with alcohols?
As chain length increases, the boiling and melting point increases
As chain length increases, the molecules get longer
As molecules get longer, there are more surface area contacts
As there are more surface area contacts, the London forces of attraction are stronger
As the London forces of attraction are stronger, more energy is required to overcome these forces of attraction so the boiling point increases
What are alcohols soluble in and why?
- alcohols are soluble in polar solvents ‘like dissolves like’
- the -OH group is polar and so are water molecules
- alcohol molecules can form hydrogen bonds with water molecules
What are the differences between alcohols and alkanes?
Alcohols are able to form intermolecular hydrogen bonds whilst alkanes are unable to
Hydrogen bonds are the strongest type of intermolecular force
Alcohols have a higher boiling point than it’s corresponding alkane i.e. propane : -42 propanol:97
Alcohols are less volatile as their boiling points are higher than alkanes
What does volatility mean?
Volatility is the tendency of a substance to evaporate
What happens when an alcohol is oxidized?
Through the process of oxidation, alcohols lose atoms of hydrogen
These atoms are lost from :
The -OH group
The carbon bonded to the -OH group
What happens when primary alcohols are oxidized?
They lose hydrogen atoms from the -OH and one hydrogen bonded to a carbon atom
Are secondary and tertiary alcohols easily oxidized?
Secondary alcohols can be easily oxidized
Tertiary alcohols can’t be easily oxidized ash it doesn’t have a H atom on the C of the C-OH group so they aren’t.
What are the conditions of the reaction of a primary alcohol to form an aldehyde?
A catalyst: sulphuric acid / acidified potassium dichromate
acidified potassium dichromate Because it is the oxidizing agent and acts as a source of oxygen
Gentle heating
Immediate distilling:if we want to obtain this aldehyde we need to immediately distill the mixture to prevent any further reaction
There should be a color change from orange to green
What happens if the mixture of the reaction between an alcohol to form an aldehyde isn’t
Distillied immediately?
And it’s conditions
A further reaction will occur to form a carboxylic acid
-heating under reflux: this is a process of constant boiling and condensing and it ensures that the reaction goes to completion and minimizes the loss of reactants and products as vapor
Excess acidified potassium dichromate
There should be a color change from. Orange to green
For the remainder :
https://www.youtube.com/watch?v=ImVzxe9jmPw&list=PLkocNW0BSuEFvnpnhj8fKN-KFUOlnKiT0&index=17