alkanes Flashcards
explain the bond angle and shape around each carbon atom in an alkane
each carbon atom is surrounded by 4 electrons in sigma bonds. repulsion between these electrons results in a tetrahedral shape and 109.5 bond angle around each carbon atom
explain the variation in boiling points of alkanes in terms of chain length
as chain length increases, boiling point increases. this is because the london forces have more points of contact between molecules and so will be stronger, requiring more energy to overcome
explain the variation in boiling points of alkanes in terms of branching
as branching increases, boiling point decreases. this is because the branches prevent the molecules from getting as closely together and also decreases the points of contact between them, making the london forces weaker (therefore less energy required to overcome)
what is homolytic fission?
each bonding atom receives one electron from the bonding pair, forming two radicals
what is heterolytic fission?
one bonding atom receives both electrons from the bonding pair
define radical
a species with an unpaired electron
what symbol is used to represent radicals in curly arrow mechanisms?
dots
what does a curly arrow represent?
the movement of a pair of electrons, showing either heterolytic fission or the formation of a covalent bond
why do alkanes have low reactivity?
C-C and C-H bonds are non polar, and have a high bond enthalpy
what are the products of the complete combustion of an alkane?
carbon dioxide and water
what are the products of the incomplete combustion of an alkane?
carbon monoxide (CO) or carbon as soot, and water
why is carbon monoxide so dangerous?
it is colourless and odourless. it reacts irreversibly with haemoglobin to form carboxyhaemoglobin, which prevents the red blood cell from carrying oxygen around the body
what do alkanes need to react with halogens (chlorine and bromine)?
UV (ultraviolet) radiation
what are the limitations of free radical substitution in organic synthesis?
-further substitution
-substitution at different positions in a carbon chain e.g. pentane could form 3 different isomers (1-bromopentane, 2-bromopentane, 3-bromopentane)