Higher Chemistry UNIT 2
Higher Chemistry Unit 2
THE WORLD OF CARBON
- Created by: Catriona Nicolson
- Created on: 26-01-12 14:49
What is petrol?
- product of crude oil
- crude oil is fractionally distilled to separate fractions
- petrol is made by reforming the naptha fraction
- blend of hydrocarbons containing between 5 and 10 carbon atoms in their chains
- blend depends on temperature
- in summer, petrol contains fewer volatile hydrocarbons
- in winter, petrol contains more volatile hydrocarbons
Petrol engine
- intake
- compression
- combustion
- exhaust
- when burnt, petrol produces waste gases
- under certain conditions the fuel can auto ignite- called knocking
- knocking reduces engine performance
- octane number of a fuel is its ability to resist knocking
- three ways to increase burning efficiency of petrol-
- 1- use alkanes with higher degree of branching
- 2- use aromatic hydro carbons
- 3- use cycloalkanes
Reforming
- reforming alters the arrangement of atoms in molecules without necessarily changing the number of carbon atoms per molecule
Advantages of alternative fuels
- reduce harmful exhaust emissions
- they do not use up a finite resource- naptha- which is obtained from crude oil
Biofuels
biofuels are fuels which come from plant or animal matter
Ethanol
- is made from sugar cane and is fermented to produce ethanol
- is renewable
- burns efficently and produces less carbon monoxide than petrol
Biogas
- mainly made up of 50-80% methane. Rest is carbon dioxide
- made form fermentation of plant and animal matter inder anaerobic conditions Bacteria act on waste materials to form biogas
Methanol
its main synthesis route is by passing synthesis gas over a heated catalyst
Advantages
- burns completely- producing less soot and carbon monoxide
- less volatile than petrol
Disadvantages
- produces half the energy of petrol
- toxic
- methanol absorbs water
Hydrogen
- can be produced by electrolysis of water
- or produced when hydrocarbons react with steam
- reduces build up of carbon dioxide in the air
Disadvantages
- hydrogen storage- is heavy in liquid or compressed form
- liquefying hydrogen is expensive
- extremely flammable
Alkanes
- Cn H2n + 2
- carbon to carbon single bonds
- name must end in -ane
Alkenes
- CnH2n
- functional group is the C=C
- name must end in -ene
Alkynes
- CnH2n-2
- functional group is the carbon to carbon triple bond
- name must end in -yne
Alkanols
- contains a hydroxyl functional group -OH
- names end in -ol
Primary Alcohol- wil have the -OH group at the end of the molecule
Secondary Alcohol- will have the -OH group in the middle of the molecule
Tertiary Alcohol- will have the -OH group in the middle of the molecule directly opposite a branch
Aldehydes and Ketones
they contain the carbonyl functional group C=O
Aldehydes
- also known as alkanals
- name will end in -al
- carbonyl always found at the end of the molecule
Ketones
- are also known as alkanones
- names end in -one
- carbonyl group will be found in the middle of the molecule
Carboxylic acids
- also known as alkanoic acids
- names end in -oic acid
- have carboxyl functional group ( COOH)
- carboxyl group at the end of the chain
Esters
- can be identified by their ester link
- are formed by the condensation reaction between an alkanoic acid and alcohol
- all ester's end in -oate
- first part of name comes from the alcohol, second part comes from the alkanoic acid.
- esters can be broken down in a hydrolysis reaction
Aromatic hydrocarbons
- simplest aromatic hydrocarbon is benzene
- has formula C6H6 and has a cyclic structural formula
- each carbon atom has 4 outer electrons. 1 is spare from each carbon atom and these form an electron cloud. They are delocalised.
- These delocalised electrons make the ring very stable.
- a benzene ring where one of the hydrogen atoms has been substituted by another group is known as the phenyl group ( C6H5)
Oxidation
most complete form of oxidation is combustion
oxidation results in an increase in the oxygen to hydrogen ratio
Primary alcohols- are oxidised first to aldehydes and then to carboxylic acids
Secondary alcohols- are oxidised to ketones
Tertiary alcohols- can't be oxidised
Reduction
Aldehydes and ketones can be returned back to their corresponding alcohols using the reducing agent, lithium aluminium hydride.
Reduction results in an increase in the oxygen to hydrogen ratio
Related discussions on The Student Room
- Hardest And Easiest Highers »
- Advanced higher as an external candidate »
- GCSE Exam Discussions 2023 »
- GCSE Exam Discussions 2024 »
- GCSE »
- How hard is the Btec level 3 extended certificate in applied science? »
- will i still get an A for higher chemistry »
- SQA Higher Exam Advice - Subject Specific »
- Access course for Pharmacy »
- I'm a "Snalien"; Plz Send Help :( »
Comments
Report
Report
Report
Report
Report