U4AOS1 - Categories, properties and reactions of organic compounds Flashcards
Relative strengths of the different forms of intermolecular bonding (strongest to weakest)
Hydrogen Bonding, Permanent Dipole-Dipole Bonding, Dispersion Force
Effect of Length of C-C chain on relative intermolecular forces
increasing the length of the carbon chain results in strongest dispersion forces (higher chance of an interaction)
Effect of Branching of C-C chain on relative intermolecular forces
branched molecules have a decreased surface area - increasing the area between molecules - thus, there is less opportunity for bonds to be formed between molecules, weaker dispersion forces
Boiling Point (+ results of weaker and stronger intermolecular forces)
temperature required to turn a substance from a liquid to a gas (break the intermolecular bonds)
Weaker IF - lower boiling point
Stronger IF - higher boiling point
Viscosity (+ results of weaker and stronger intermolecular forces)
the resistance of a substance to flow
Weaker IF - lower viscosity (less energy is required to break bonds)
Stronger IF - higher viscosity (more energy required to break bonds)
Effect of Temperature on Viscosity
when substances are heated, viscosity will decrease, as more energy is available to overcome the intermolecular forces
Flashpoint (+ results of weaker and stronger intermolecular forces)
lowest temperature at which an organic compound can ignite in the air
Weaker IF - lower flashpoint
Stronger IF - higher flashpoint
Is flashpoint greater or less than boiling point?
Given flashpoint relates to liquid fuels - flashpoint must be lower than boiling temperature
Addition Reactions (+ pathways)
The breaking of the C=C bond, to produce a hydrocarbon
- Addition of H2 - requires a metal catalyst (Pt, Pd or Ni)
- Addition of H2O (produces alcohols) - requires H3PO4 (or H+) @ 300 degrees
- Addition of other reactants - doesn’t require a catalyst
Bromine Test
Type of addition reaction - checks for the presence of double bonds
if the solution is colourless - unsaturated hydrocarbons are present
if the solution remains red-brown - bromine didnt react
Substitution Reactions (+ pathways)
Reactions where one or more of the hydrogen atoms are replaced by another atom or functional group
- Substitution of Halogen (requires UV light) - position it will replace can be determined by the story of the question
- Substitution of Haloalkanes (to produce alcohol) - requires a source of OH- (generally Na, or K)
- Polar group substitution (no catalysts)
Oxidation of Alcohols
Requires an Oxidizing Agent: can be any acid (must include H+) - e.g. MnO4- or Cr2O7 2-
Primary Alcohols - converted to aldehydeds -> carboxylic acids
Secondary Alcohols -Ketones
Tertiary Alcohols - cannot be oxidized
Esterification Reactions
Combinedd an alcohol and carboxylic acid
Requires Concentrated Sulfuric acid H2SO4 (l)
Atom Economy
(include molar ratios)
Yield of Reactions