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Flashcards for reviewing functional groups and their naming conventions in organic chemistry.
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Alkene
Compound with a double bond, ending in -ene (e.g., Propene)
Alkyne
Compound with a triple bond, ending in -yne (e.g., Propyne)
Arene
Aromatic compound (e.g., Benzene), no specific ending
Halide
Compound with a halogen (F, Cl, Br, I, e.g., Iodoethane), no specific ending
Alcohol
Compound with -OH group, ending in -ol (e.g., Ethanol)
Ether
Compound with -O- linkage (e.g., Ethoxyethane or Diethyl ether), named as ether
Aldehyde
Compound with a carbonyl group at the end of the chain, ending in -al (e.g., Ethanal)
Ketone
Compound with a carbonyl group in the middle of the chain, ending in -one (e.g., 2-Propanone)
Ester
Compound with -COOC- linkage, ending in -oate (e.g., Ethyl Ethanoate)
Carboxylic Acid
Compound with -COOH group, ending in -oic acid (e.g., Butanoic acid)
Amide
Compound with -CON- linkage, ending in -amide (e.g., Ethanamide)
Amine
Compound with -NH2 group, ending in -amine (e.g., Ethylamine)
Nitrile
Compound with -CN group, ending in -nitrile (e.g., Ethanenitrile)
Nitro
Compound with -NO2 group, using nitro as a prefix (e.g., Nitroethane)
Thiol
Compound with -SH group, named thiol (e.g., Methyl thiol)
Organometallic
Compound with a metal-carbon bond (e.g., Methyl lithium), no specific ending