Module 4.2 - Alcohols, Haloalkanes and Analysis Flashcards
What is the general formula of alcohols?
C(n)H(2n+1)OH
Describe primary alcohols
Alcohol attached at the end of the chain with one alkyl chain attached.
Describe secondary alcohols
Alcohol attached to 2 alkyl chains and a hydrogen atom.
Describe tertiary alcohols
Alcohols attached to 3 alkyl chains
Describe the trend in boiling points of alcohols.
> Increases as chain length increases.
More surface area contacts
Stronger induced dipole-dipole IMFs
More energy needed to overcome IMFs.
Compare the boiling points of alcohols with their corresponding alkanes.
Alcohols have a higher boiling points than their corresponding alkanes due to hydrogen bonding in which are stronger than induced dipole-dipole interactions (London forces)
What does the volatility of alcohols mean?
How easily alcohols evaporate at RTP.
Describe the volatility of alcohols
Volatility increases as boiling points decrease. Therefore short chain alcohols are the most volatile.
Compare the volatility of alcohols with their corresponding alkanes.
Alcohols have hydrogen bonding which means that they are less volatile than their corresponding alkanes as their boiling points are higher on average.
Describe the solubility of alcohols
Alcohols are soluble in water as water molecules are polar and so is the functional group, therefore hydrogen bonds can be formed with the molecules.
Define nucleophile
An electron pair donor.
What happens as CFCs are exposed to UV light?
The C-Cl bonds undergo homolytic fission creating chlorine radicals.
What is the problem with chlorine radicals being formed by CFCs in the environment?
They catalyse the decomposition of ozone. The chlorine radicals attack the ozone molecules and turns them into diatomic oxygen.
What is the result of chlorine radicals converting ozone?
The ozone layer is shrinking and in some places there is no ozone in the upper stratosphere or low troposphere.
What causes covalent bonds to vibrate more and absorb energy?
Infrared radiation