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HYDROCARBON DERVIATIVES - Coggle Diagram
HYDROCARBON DERVIATIVES
OXYGEN DERIVATIVES
ALDEHYDES
Naming: IUPAC: The alkane name is changed to -al. Common: the first five aldehydes use prefixes: form (1c), acet (2c), propion (3c), butyr (4c) and valer (5c).
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KETONES
Naming: IUPAC: The alkane is replaced with -one. Common: alkyl groups are attached to the carbonyl group alphabetically and add ketone. Ex. propanone (dimethyl ketone)
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ETHERS
Naming: Take names of the alkyl group written as separate words in alphabetical order. the word ether is added at the end , adding the name of the radicals in alphabetical order.
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CARBOXYLIC ACIDS
Naming IUPAC: replacing the -e, name the longest chain with -oic acid. Common: using prefixes form (1c), acet (2c), propion (3c), butyr (4c) and valer (5c).
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ALCOHOLS
Structure: R-OH
Naming
IUPAC: replaces -e in alkane name with -ol ex. methanol, ethanol. (with longer chains, number from the end nearest to -OH. Common: alkyl followed by alcohol ex. methanol (methyl alcohol)
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ESTERS
Naming Changing the -ic ending to -ate and adding the name of the corresponding radical. IUPAC: methyl ethanoate. Common: methyl acetate
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HALOGEN DERIVATIVES
HALOALKANES
Dihalogen derivatives
Contain two halogen atoms per molecule, ex. CH2CI2 (Dichloromethane or methylene chloride)
Trihalogen derivatives
Contain three halogen atoms per molecule, ex. CHCI3 ( trichloro methane or chloroform)
Monohalogen derivatives
Contain one halogen atom per molecule, ex. CH3CI (chloromethane or meethyl chloride)
Tetrahalogen derivatives
Contain four halogen atoms per molecule, ex. CCI4 ( tetrechloro methane or carbon tetrachloride)
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