The boiling points of several alkanols are provided in the following table - VCE - SSCE Chemistry - Question 9 - 2010 - Paper 1
Question 9
The boiling points of several alkanols are provided in the following table.
Alkanol Boiling point (°C)
methanol 64.5
ethanol 78.3
propan-1-ol 9... show full transcript
Worked Solution & Example Answer:The boiling points of several alkanols are provided in the following table - VCE - SSCE Chemistry - Question 9 - 2010 - Paper 1
Step 1
Identify one alkanol that could not be present in this mixture.
96%
114 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The alkanol that could not be present in this mixture is butan-1-ol.
Step 2
By specifically referring to this experiment, explain why the alkanol identified in part i. could not be present.
99%
104 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
Butan-1-ol cannot be present because it has a boiling point of 117.2 °C, which is higher than the first fraction collected at 97.2 °C. If butan-1-ol were included in the mixture, it would have remained in the distillation flask and would not be collected as part of the distillate at that temperature.
Step 3
Provide one reason why the distillation flask should not be heated using a Bunsen burner.
96%
101 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The distillation flask should not be heated with a Bunsen burner because the flame may be too hot and could cause the contents to boil too violently, increasing the risk of vaporization and possible explosion of flammable vapors.
Step 4
Explain, in terms of intermolecular forces, the difference between the boiling points of these two compounds.
98%
120 rated
Only available for registered users.
Sign up now to view full answer, or log in if you already have an account!
Answer
The higher boiling point of propan-1-ol compared to butane is primarily due to the presence of hydrogen bonding in propan-1-ol. In butane, the predominant intermolecular forces are London dispersion forces, which are weaker than the hydrogen bonds found in propan-1-ol. Consequently, more energy is required to overcome the intermolecular forces in propan-1-ol, resulting in a higher boiling point.