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hydroxide
OH-
hydronium
H3O+
ammonium
NH4+
nitrate
NO3-
nitrite
NO2-
chlorate
ClO3-
chlorite
ClO2-
carbonate
CO32-
hydrogen carbonate/bicarbonate
HCO3-
cyanide
CN-
acetate
C2H3O2-
sulfate
SO42-
phosphorus
PO43-

linear
electron pairs: 2
lone pairs: 0

trigonal planar
electron pairs: 3
lone pairs: 0
120

Bent
electron pair: 3
lone pairs: 1
<120

tetrahedral
electron pair: 4
lone pair: 0
109

trigonal pyramid
electron pairs: 4
lone pairs: 1
109
bent
electron pairs: 4
lone pairs: 2
«109
molecular shape: tetrahedral
4 bonds to C all single
molecular shape: trigonal planar
3 bonds to C double w/ 2 single
molecular shape: linear
2 bonds to C triple w/ 1 single or 2 doubles
saturated
all single bonds & max number of hydrogens
noncyclic (no rings) formula
CnH2n+2
alkane
single bonds
alkene
double bond
alkyne
triple bond
meth- (methane)
1
eth- (ethane)
2
prop- (propane)
3
but- (butane)
4
pent- (pentane)
5
hex- (hexane)
6
hept- (heptane)
7
oct- (octane)
8
non- (nonane)
9
dec- (decane)
10
1 unsaturated ring
-2H
1 unsaturated double
-2H
1 unsaturated triple
-4H
naming compounds
substituents (attachments) + parent name (number of carbons) + suffix (family name)
constitutional/skeletal
different connections
stereoisomers
same connection but different 3D
geometric
C double bond C + ring (can’t rotate)
conformational
rotate how one single bond is drawn
optical
4 different groups attached to 1 C
enantiomer
flip all wedges to dashes and dashes to wedges
trans
one wedge and one dash
cis
two wedges or two dashes
alcohol

alkene

alkyne

amide

aromatic

carboxylate

carboxylic acid

disulfide

ester

ether

haloalkane

ketone

phenol

phosphate

Thiol

thioether

primary amine

secondary amine

tertiary amine

amine

aldehyde
