Chapter 9 - Properties of Organic Compounds Flashcards
Describe dispersion
- non polar regions form instantaneous dipoles.
- weak but accumulative with more electrons
Describe dipole-dipole
- polar molecules form permanent dipoles
- opposing charges on neighbouring molecules are electrostatically attracted to each other.
Describe hydrogen bonding
-present when H is bonded to N,O,F. A neighbouring atom must also contain an electronegative element. These are the strongest due to hydrogens little shielding affect and small size.
Describe flashpoint
The flashpoint of a volatile liquid is the lowest temperature at which the liquid gives off enough vapour to ignite. weaker intermolecular forces = lower flashpoint as molecule is more volatile
Describe points
points refer to melting and boiling point. A high boiling point=strong intermolecular forces. A high melting point=more energy needed to push molecules away from each other.
Describe viscosity
-the thickness of a substance (degree of flow)
high viscosity= very thick= no flow
low viscosity= not thick= lots of flow
Hierarchy of hydrogen bonding and functional groups
carboxylic acids- QQQQQQQQQQQQQQQQ alcohols- amines/amides- carbonyl/ester- only dipole basic hydrocarbons- only dispersion
What are structural isomers
structural isomers can be
- chain (different branching)
- positional (different position of functional group)
- functional (different functional group but same atoms)
What is Stereoisomerism
where molecules are arranged differently around a double or triple bond. Only one common pair has to be used. CIS on the same side TRANS on opposite sides
What is Enantiomerism (optical isomers)
- shown by a chiral centre
- mirror images are not superimposable
- carbon is bonded to 4 different molecules
- bend polarised light in opposing ways
what are the functional isomer pairs?
alcohols—-ethers
carboxylic acids—-esters
aldehydes—-ketones