4.2 - Alkanes Flashcards
Type of bond alkanes have
single covalent σ bonds which can rotate freely
Define sigma bond
overlap of 2 orbitals, 1 from each bonding atom, positioned on line directly between bonding atoms
Bond angle around each carbon in alkanes and shape
109.5°
tetrahedral
Why would an alkane have a higher BP?
- increased chain length
- more points of surface contact
- stronger London forces
- more energy needed to overcome LFs
Why would an alkane have a lower BP?
- more branching
- less points of surface contact
- weaker London forces
- less energy needed to overcome LFs
Chemical properties of alkanes
- not very reactive due to strong and non-polar C-C/C-H bonds
- used as fuels because readily available, easy to transport, burn to release no toxic products
Name and describe with equations the mechanism for ethane reacting with chlorine
- radical substitution
initiation: Cl2 -> 2Cl* (requires UV)
propagation: C2H6 + Cl* -> C2H5* + HCl
C2H5* + Cl2 -> C2H5Cl + Cl*
termination: 2Cl* -> Cl2
2C2H5* -> C4H10
C2H5 + Cl* -> C2H5Cl
What are the limitations of radical substitution?
- further substitutions can occur
- substitution at different positions in C chain
(forming a mixture of organic products)
Why are alkanes not very reactive?
high bond enthalpy and very low polarity of σ-bonds
What are the potential dangers of CO?
toxic
State the general equation for complete combustion of an alkane
alkane + O2 -> CO2 + H2O
State the general equation for incomplete combustion of an alkane
alkane + O2 -> CO + C + H2O