Unit 4 Flashcards
(53 cards)
Hydrocarbon?
Molecule with just carbons and hydrogens
Alkane?
Carbon and hydrogen only - saturated molecules
What intermolecular forces interact with alkanes?
Dispersion
What happens as the size of an alkane increases, in regards to its boiling point?
The larger the alkane, the increased strength and thus BP.
Larger =
- more atoms/surface area of interaction
- more electrons (which are dispersion forces)
- more dispersion
- INCREASE needed energy to break bonds
- Increase BP
What is dispersion forces?
Electrons orbit in each adjacent molecules, causing temporary dipoles
How do cyclic hydrocarbons similar to straight line carbon chains
similar chemical and physical properties
What can affect boiling point in alkanes?
Molar Mass (more electrons) thus heavier halogen has higher BP - (I > Br > Cl > F)
Branching
Size of ALKANE - length
How does branching in alkanes affect boiling point?
Molecules stack poorly against each other
Area of interaction smaller
LESS dispersion forces
LOWER (BP)
How does hydrogen bonding work and whats needed?
A H-FON bond within a molecule
- forming a partial charge (with partial negative on electronegative hydrogen FON)
- bonds with positive side on a hydrgeon on another atom
What does saturated mean in a hydrocarbon?
Saturated - single bonds, alkane, less reactive
Unsaturated - more than single bond (double, triple) - alkene, alkyne, more reactive
Which cyclocarbons are saturated vs unsaturated
Saturated - cycloalkane
Unsaturated - cycloalkene/alkyne
Whats Benzene?
C6H8
double bond every second carbon - but bond length/type in benzene are all the same
- electrons delocalise thus really stable
Hexagon with circle in middle (to represent delocalised electron cloud) located above and below the ring
Aromatic in QCAA?
Mean stuff like benzne
But also smelly stuff - esters
Saturated vs unsaturated as fuels
SATURATED
- single bonds only - stronger - more energy to break (thus release more energy which is what fuel is as) - thus alkanes and alchols
- unsaturated have double/triple bonds - weaker - can lead to different products and potential of incomplete combustion - CO/soot
Why are alkanes used as fuels
Because they release energy well and smaller ones vaporise well (VOLATILITY)
What does volatile mean?
The ability to change from liquid to gas (vaporise) - at lower boiling points or smaller alkanes
How does alkane size affect flammability?
Smaller alkanes are more volatile as they vaporise quicker - liquid to gas
Complete combustion?
burn alkane in excess oxygen to form CO2 (carbon dioxide) and water
- keep in mind co2 is greenhouse gas
Simple Substitution
Replacing one species on molecule with another
I.e.
C2H5Br +HCL –> C2H5Cl + HBr
Haloalkane + hydrogen halide –> Haloalkane + hydrogen halide
Simple Condensation
When small molecule is lost in formation of a larger molecule + water
I.e.
CH3COOH + CH3OH –> CH3COOCH3 + H2O
methanoic acid (acetic acid) + methanol –> methyl ethanoate (methyl acetate)
Carboxylic Acid + Alcohol –> Ester
Simple Reduction
Species gain electrons
- when electromagnetic atom - like oxygen is removed from a molecule
Simple Addition
Joining 2/more molecules to form a larger molecule
C2H4 +H2 –> C2H6
Alkene + hydrogen –> alkane
Simple Polymerisation
Joining many simple molecules to form a giant one
- reacting monomer molecules together in a chemical reaction to form polymer chain (polymers)
Simple Elimination
Removing small group of atoms from a larger molecule C2H5OH –> C2H4 + H2O