Chapter 22: Alkenes and Acids
Means that alkenes have two fewer hydrocarbons
They are unsaturated as they contain the same number of hydrogen and carbon atoms, unlike alkanes which are saturated as they contain different amounts of hydrogen and carbon
Bond can open, allowing the two carbon atoms to bond with other atoms, which makes them far more reactive than alkanes
First four are ethene, propene, butene, pentene
Alkenes normally combust completely if there’s enough oxygen
However, there isn’t enough oxygen in the air of this, so they undergo incomplete combustion
Alkenes + oxygen - carbon + carbon monoxide + carbon dioxide + water(+energy)
Result in a smokey yellow flame and less energy being released
The carbon-carbon double bond will open up and add additional atoms on
New atoms are added to each carbon
Open up the double bond and form the equivalent saturated alkane
Needs a catalyst
Water is added across the double bond and an alcohol is formed
For example ethene and water makes ethanol
After reactions, mixture is passed from the reactor into a condenser
Ethanol and water have a higher boiling point then ethene so both condense whilst any unreacted ethene gas is recycled back into the reactor
Alcohol can then be purified through fractional distillation
Halogens include bromine, chlorine and iodine
Molecules formed are saturated, with the C=C carbons each becoming bonded to a halogen atom
Form di(halogen-ine)(alkane)
The addition of bromine to a double bond can be used to test for alkenes
When orange bromine water is added to a saturated compound, like an alkene, no reaction will happen and it remains bright orange
If it’s added to an alkene the bromine will add across the double bond making a colourless dibromo-compound, so the bromine water is decolourised
Test for alkene and how it works?
Add bromine water to the solution, if alkane present it turns from orange to colourless
Works as the bromine will add across the double bond making a colourless dibromoethene compound
Reaction with halogens
Molecules formed are saturated with the C=C carbon each becoming bonded to a halogen atom
Reaction with hydrogen
Open up the double bond and form the equivalent saturated alkane, and needs a catalyst to work
Reaction with water
Water is added across the double bond, alcohol is formed this way
Means that alkenes have two fewer hydrocarbons
They are unsaturated as they contain the same number of hydrogen and carbon atoms, unlike alkanes which are saturated as they contain different amounts of hydrogen and carbon
Bond can open, allowing the two carbon atoms to bond with other atoms, which makes them far more reactive than alkanes
First four are ethene, propene, butene, pentene
Alkenes normally combust completely if there’s enough oxygen
However, there isn’t enough oxygen in the air of this, so they undergo incomplete combustion
Alkenes + oxygen - carbon + carbon monoxide + carbon dioxide + water(+energy)
Result in a smokey yellow flame and less energy being released
The carbon-carbon double bond will open up and add additional atoms on
New atoms are added to each carbon
Open up the double bond and form the equivalent saturated alkane
Needs a catalyst
Water is added across the double bond and an alcohol is formed
For example ethene and water makes ethanol
After reactions, mixture is passed from the reactor into a condenser
Ethanol and water have a higher boiling point then ethene so both condense whilst any unreacted ethene gas is recycled back into the reactor
Alcohol can then be purified through fractional distillation
Halogens include bromine, chlorine and iodine
Molecules formed are saturated, with the C=C carbons each becoming bonded to a halogen atom
Form di(halogen-ine)(alkane)
The addition of bromine to a double bond can be used to test for alkenes
When orange bromine water is added to a saturated compound, like an alkene, no reaction will happen and it remains bright orange
If it’s added to an alkene the bromine will add across the double bond making a colourless dibromo-compound, so the bromine water is decolourised
Test for alkene and how it works?
Add bromine water to the solution, if alkane present it turns from orange to colourless
Works as the bromine will add across the double bond making a colourless dibromoethene compound
Reaction with halogens
Molecules formed are saturated with the C=C carbon each becoming bonded to a halogen atom
Reaction with hydrogen
Open up the double bond and form the equivalent saturated alkane, and needs a catalyst to work
Reaction with water
Water is added across the double bond, alcohol is formed this way