4.1.2. Alkanes Flashcards
Formation of a sigma bond in alkanes
One sp3 orbital from each carbon overlap to form a single C-C bond called a sigma bond
Boiling points
Increasing boiling points of alkanes can be explained by increasing number of electrons in the bigger molecules
Increases size of induced dipole-dipole interactions between molecules
Longer straight chains have a larger surface area of contact between molecules for London forces to form so have strong induced dipole interactions and higher boiling points
Reactivity
Low reactivity of alkanes with many reagents
Due to high bond enthalpies of c-c and c-h bonds
Low polarity of sigma bonds
cracking
Conversion of large hydrocarbons to smaller molecules by breaking c-c bonds
Reasons for cracking
Petroleum fractions with shorter c chains are in more demand than larger fractions
To make use of excess larger hydrocarbons to supply demand for shorter ones
Products of cracking more valuable than starting materials
Catalytic cracking
Slight pressure
High temperature (450C)
Zeolite catalyst
used for making motor fuels
reaction of alkanes with bromine/cl2
UV light
homolytic fission - each atom gets one electron from the covalent bond
free radical
reactive species which possess an unpaired electron