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24 Cards in this Set

  • Front
  • Back
Methyl
R-CH3
Ethyl
R-CH2-CH3
Phenyl
R-Benzene ring (C6H5)
Aldehyde
R-C[=O]-H

(Note: the C is double bonded to the O, and single bonded to the H)
Ketone
R-C[=O]-R'

(Note: the C is double bonded to the O, and single bonded to the R')
Carboxylate
R-C[=O]-O(-)

(Note: the C is double bonded to the O, and single bonded to the negative O)
Hydroxyl (Alcohol)
R-OH
Enol
R-CH[OH]=CH2

(Note: the first C is double bonded to second C, and single bonded to the H and OH)
Ether
R-O-R'
Ester
R-C[=O]-O-R

(Note: the C is double bonded to the first O, and single bonded to the second)
Acetyl
R-O-C[=O]-CH3

(Note: the C is double bonded to the O, and single bonded to the C of the methyl group)
Anhydride
R-C[=O]-O-C[=O]-R'

Note: Both carbons are double bonded to one O and single bonded to the other.
Amine
R-NH2
Amido
R-C[=O]-NH2
Imine
R-C[=NH]-R'

Note: Carbon double bonded to N, which is single bonded to H.
N-Substituted Amine (Schiff Base)
R-C[=NR"]-R'

Note: Carbon double bonded to N; the N is bonded to a third R group.
Guanidinium
R-N[-H]-C[=N(+)H2]-NH2

The backbone in R-NH-C-NH2. The Carbon is also double bonded to a second NH2 group where N+
Imidazole
Think of a pentagon, with the point facing up like a house. The bottom floor is R-C=CH. The middle floor, above the Cs, is NH and N. The peak is C, double bonded to N, single to NH.
Sulfhydryl
R-SH
Disulfide
R-S-S-R'
Thioester
R-C[=O]-S-R'
Phosphoryl
R-O-P[-O(-)][=O]-OH

Note: P is bound to four oxygens. The first is a single bond, second single(top) with O negative, the third with OH, and fourth (bottom) a double bond.
Phophoanhydride
Backbone: R-O-P-O-P-O-R"

Each P also has an O negatively charged, single bond above, and an O double bonded below.
Mixed Anhydride
R-C-O-P-OH

Both Carbon & P are also double bonded to an O. P also has a single bond to an additional negatively charged O.