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A comprehensive vocabulary set of functional groups including hydrocarbons, halogens, oxygen, nitrogen, and sulfur-containing structures based on medicinal chemistry lecture slides.
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Alkane (single bond)
A hydrocarbon containing only single covalent bonds.
Alkene (double bond)
A hydrocarbon containing at least one carbon-carbon double bond.
Alkyne (triple bond)
A hydrocarbon containing at least one carbon-carbon triple bond.
Aromatic hydrocarbon (benzene)
A cyclic, planar hydrocarbon with delocalized pi systems, such as benzene.
Halogen
Elements from Group 7 of the periodic table, including F, Cl, Br, I, and At.
Hydrogen Bond Donor
A group with a hydrogen atom bonded to an electronegative atom, such as N−H or O−H, capable of forming a hydrogen bond.
Hydrogen Bond Acceptor
An electronegative atom with a lone pair, such as oxygen, nitrogen, or fluorine, that can attract a hydrogen bond donor.
Alcohol
An oxygen-containing functional group characterized by the structure R−O−H.
Ether
An oxygen-containing functional group with the structure R−O−R.
Aldehyde
A carbonyl-containing functional group with the structure R−CHO.
Ketone
A carbonyl-containing functional group with the structure R−CO−R.
Carboxylic Acid
A carbonyl-containing functional group with the structure R−COOH.
Acid Halide
A carbonyl-containing functional group bonded to a halogen with the structure R−COX.
Ester
A carbonyl-containing functional group with the structure R−CO−OR.
Amide
A functional group in which a carbonyl carbon is bonded to a nitrogen atom.
Amine
A nitrogen-containing functional group typically structured as R−NH2, R2NH, or R3N.
Nitro
A nitrogen-containing functional group with the structure −NO2.
Nitrate
A nitrogen-containing functional group with the structure −O−NO2.
Nitrile
A nitrogen-containing functional group with a carbon atom triple-bonded to a nitrogen atom (R−C⨄N).
Imide
A nitrogen-containing functional group consisting of two carbonyl groups bonded to the same nitrogen atom.
Guanidine
A nitrogen-containing functional group with the central structure H2N−C(=NH)−NH2.
Imine
A nitrogen-containing functional group characterized by a carbon-nitrogen double bond (C=N).
Amidine
A nitrogen-containing functional group with the structure R−C(=NH)−NH2, similar to a carboxylic acid derivative.
Carbamate
A functional group that contains both an ester and an amide moiety bonded to the same carbonyl.
Urea
A functional group where a carbonyl carbon is bonded to two different nitrogen atoms.
Thiol
A sulfur-containing functional group characterized by the structure R−SH.
Sulfide (thioether)
A sulfur-containing functional group with the structure R−S−R, analogous to an ether.
Thioketone
A sulfur-containing functional group where a carbon atom is double-bonded to a sulfur atom (C=S).
Thiocarboxylic acid
A sulfur-containing analogue of a carboxylic acid where one or more oxygen atoms are replaced by sulfur.
Thioester
A sulfur-containing analogue of an ester with the structure R−CO−SR.
Disulfide
A sulfur-containing functional group consisting of a bond between two sulfur atoms (R−S−S−R).
Sulfoxide
A sulfur-containing functional group where a sulfur atom is double-bonded to one oxygen and single-bonded to two alkyl or aryl groups.
Sulfinic acid
A sulfur-containing functional group with the structure R−S(=O)OH.
Sulfone
A sulfur-containing functional group where a sulfur atom is double-bonded to two oxygen atoms and single-bonded to two alkyl or aryl groups (R−SO2−R).
Sulfonic acid
A sulfur-containing functional group with the structure R−SO2−OH.
Sulfonate ester
A sulfur-containing functional group with the structure R−SO2−OR.
Sulfonamide
A sulfur-containing functional group with the structure R−SO2−NH2.