Organic Chemistry Flashcards
Aldehyde
R-CHO (double bonded O)
Can be prepared from the oxidation of an alcohol.
To name aldehydes, drop the -ol from alcohol name and replace with -al (ex. Methanol becomes methanAL)
Ethanol (C2H5OH)
AKA ethyl alcohol and grain alcohol. Colorless, flammable liquid.
Boiling point of 78 degrees Celsius. Miscible with water, good solvent (forms solutions commonly known as tinctures).
Can be used as antifreeze b/c freezing point is -115 degrees Celsius.
Used to make acetaldehyde and ether.
Methanol (CH3OH)
AKA wood alcohol.
Colorless, flammable liquid w/ bp of 65*C. Miscible with water, poisonous, can cause blindness if swallowed. Can be used as fuel, solvent, denaturant to make ethanol. Unsuitable for drinking.
Ethylene Glycol
1,2-ethanediol
Colorless, high bp, low fp. Used as permanent antifreeze.
Glycerine or glycerol
1,2,3-propanetriol
Colorless, odorless, viscous, sweet liquid. Used to make nitroglycerine, resins for paint, and cellophane.
Methanal
Formaldehyde
Ethanal
Acetaldehyde
Carboxylic (Organic) Acids
R–COOH
Made from mild oxidation of aldehyde.
Named with -oic (ex. Methanal forms MethanOIC acid)
Methanoic Acid
Formic Acid
Ethanoic Acid
Acetic Acid (CH3COOH)
Glacial acetic acid
Concentrated acetic acid (ethanoic acid). Used to make cellulose acetate.
Ketones
R-C-R*
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O
Formed from a slightly oxidized secondary alcohol.
Named by adding # for which carbon has double bonded O then adding -one. (Ex. Butan-2-ONE has double bond on 2nd carbon and it has 4 carbons total)
Ether
R-O-R*
Formed by dehydration of primary alcohol with sulfuric acid.
Shorter chain is first half of ether’s name with -ane suffix changed to-OXY and longer alkane chain name is suffix (ex. If propane-O-ethane, name is ethoxypropane or ethyl propyl ether)
Diethyl Ether
Commonly called ‘ether’
Anesthetic
Amine
Compound where NH2- (amide ion) replaces a hydrogen in a hydrocarbon.