12 Alkanes Flashcards
Free Radical Substitution
- Initiation
- Propagation
- Termination
Reagents and conditions: (limited) X2, UV light
General formula for alkanes
C(n)H(2n+2)
Cycloalkanes
Saturated cyclic hydrocarbons which form a closed ring structure
Melting and boiling points of alkanes
Increases as number of carbon atoms increases
Strength of id-id interactions between molecules increases as number of electrons increases
Density of alkanes
Less dense than water
Packing of alkane molecules less efficient than water
Weaker id-id interactions between alkane molecules as compared to stronger hydrogen bonds between water molecules
Increase in density as number of carbon atoms increases (increase in molar mass>increase in volume)
Solubility of alkanes in water
Insoluble in water
Water is a polar solvent; alkanes are non-polar -> cannot form effective interactions with water molecules
Energy needed to overcome stronger hydrogen bonds between water molecules > energy released when weaker id-id interactions form between alkanes and water
Reactivity of alkanes
Relatively unreactive
Non-polar C-C and C-H bonds -> unreactive towards polar reagents
C-C and C-H bonds very strong
Combustion of alkanes
C(x)H(y) + (x+y/4)O2 -> xCO2 +y/2 H2O
Stability of hydrocarbon radicals
More substituted radical, more stable the radical
Alkyl substituents are weakly electron-donating, which helps to stabilize the electron deficient carbocation
Cracking
Bigger hydrocarbon molecules are broken down into smaller molecules