4.1.2 Flashcards
(9 cards)
Why are alkenes relatively unreactive
The C–C and C–H bond enthalpies are relatively high so require a lot of energy to break
What type of IMF do alkanes have
London dispersion forces (they are non-polar)
What happens to bp as alkane chain length increases
Increases as there is more surface area so more LDF. More energy is required to break the bonds
What is the equation of complete combustion
Alkane + Oxygen —-> Carbon dioxide + Water
What is the equation of incomplete combustion
Alkane + Oxygen —-> Carbon/ carbon monoxide + Water
What are the 3 steps of free radical substitution
Initiation- forms 2 free radicals
Propagation- FR + molecule —> FR + molecule
Termination- FR + FR —> molecule
What are the steps of free radical substitution in the synthesis of bromoethane
I) BR-BR —> 2BR•
P) C2H6 + BR• —> •C2H5 + HBr
•C2H5 + Br2 —> C2H5Br + Br•
T) •Br + •BR —> Br2
•C2H5 + • C2H5 —> C4H10
•C2H5 + •Br —> C2H5Br
What conditions does initiation require
UV light
What are the problems with free radical substitution
Has a low atom economy
It is hard to predict the final product
It can happen at any point of the carbon chain