Alkanes + Cyclo Flashcards
According to old names a propane substituent bonded at the middle is called what?
Isopropyl
What is a primary carbon?
One which is bonded to 1 other carbon
What is a secondary carbon?
One which is bonded to 2 other carbons
What is a tertiary carbon?
One which is bonded to 3 other carbons
What happens to melting/ Boiling points as the carbon chain gets longer and why?
They increase due to stronger London dispersion forces
What are London dispersion forces?
When electrons repel each other creating temporary delta positives and negatives, thus a temporary dipole.
Theyre really weak intermolecular interactions
Do branched alkanes have higher or lower melting boiling points than straight chains?
Lower, they’re harder to pack and therefore experience less temporary dipoles (London dispersion forces)
Are alkanes reactive?
Quite unreactive due to strong c-c
But can have reactions eg with chlorine gas and can be burnt (oxidisation)
Why do we burn alkanes?
The c-c bond is really strong, so when burnt it releases a lot of energy which can be used.
What is a constitutional isomer?
It has a different structural arrangement, different connectivity
What is an molecule isomer?
Different molecules that have the same molecular formula. So can be arranged differently etc
What does a staggered conformation mean?
When atoms are in the form with lowest energy. they face the least repulsion, atoms are as far apart as possible within the molecule
What does an eclipsed conformation mean?
Molecule has rotated in a way in which atoms are overlapping. Electrons repel each other therefore this form is a high energy form
What is the anti conformation?
When the molecule has rotated in a way in which no atoms are overlapping, it has the least repulsion between atoms and is therefore the most stable
What is the gauche conformation?
When the molecule has rotated in such a way that it is staggered but there may be some groups overlapping so it is higher in energy than the anti conformation