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Chemistry
Module 4
Chapter 12
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Cards (18)
What are properties of alkenes?
Very
stable
Main component in natural
gases
and
crude oil
Can be extracted using
fractional distillation
Effect of branching of alkenes boiling points?
Increased
branching
means that there are fewer points of surface contact
There are fewer
London
forces
Molecules are therefore further apart
Weaker
London
forces requires less energy is order to break
Lower boiling points
What is the bonding in alkanes?
each carbon atom is joined to
four
other atoms by single covalent bonds -
sigma
bonds
What is a sigma bond?
Is the
overlap
of atomic orbitals directly between the bonding atoms
representing a shared pair of electrons (a covalent bond)
Define homolytic fission
each of the
bonded
atoms takes one of the shared pair of
electrons
Define heterolytic fission
one of the
bonded
atoms takes bother of the electrons from the
bond
What is a radical?
a species with an
unpaired
electron
What do you use to show movement of an electron pair when bonds are broken or made?
Curly arrows
What is an
addition reaction
?
two reactant molecules join together to form
one
product (atom economy =
100
%)
What is a
substitution reaction
?
an atom or group of atoms is
replaced
by a
different
atom or group of atoms
What is an elimination reaction?
a
small
molecule is removed from a
large
molecule
What is the reactivity of alkanes?
Sigma
bonds are very strong
Non-polar
molecules - can't use heterolytic fission
Electronegativity
of carbon and hydrogen atoms are so similar that
C-H
bond is also considered non-polar
Ea
is very high
Combustion of alkanes?
Give out energy when reacted with oxygen.
Show two different equations when showing incomplete combustion.
(carbon dioxide OR carbon)
Used as fuels because the energy is readily available - easy to transport
What is needed for reaction of alkanes and halogens?
UV radiation
(aka -
sunlight
)
What are observations of bromine reaction with C5H12
Bromine is
decolourised
Moist litmus paper turns
red
(acidic)
What is the reaction between halogens and alkanes?
Substitution
reaction - hydrogen replaced by
bromine
atom
UV radiation
is required for initial energy of reaction - no UV =
bromine remains red-brown
What are the stages of halogenation mechanism of alkanes?
Initiation
(formation of radicals via homolytic fission)
Propogation
(radicals on both sides of the equations - chain reaction)
Termination
(two radicals collide to form molecule with both electrons paired - stopping the chain reaction)
What happens when further substitution occurs?
Once
haloaklane
is formed in propogation, another
bromine
radical can attack it to form a dihaloaklane
This can continue until all
hydrogen
atoms have been substituted with
bromine
We cannot control where on the
chain
the radical will attack!