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Constitutional Isomers
same chemical formula, different connections
Resonance
molecules don’t rotate, move, or change bond angles, only arrangement of e- change
Delocalized
state when e- are spread out across atoms in resonance
Localized
state when e- are “stuck” between 2 atoms (in a bond) or on an atom (lone pair)
Vinylic
carbons in a double bond
Allylic
carbons “next-door” to a double bond
Allylic Lone Pair
lone pair → π bond, π bond → lone pair
Allylic Carbocation
π bond → π bond “next door”
Lone Pair Adjacent to a Carbocation
lone pair → π bond
Pi Bond Between 2 Atoms of Differing Electronegativity
π bond → Oxygen (ex.)
Conjugated Pi Bonds Enclosed in Ring
π bonds rotate one space about an enclosed ring of carbons
Locant
a number that indicates the position
Torsional Strain
energy cost associated with the loss of the eclipsed conformation
Steric Interaction
e- clouds are too close and repel each other
gauche
steric interaction only found in staggered confromation
Stereoisomer
same chemical formula, differ in spatial arrangement
Conformers (Confirmational Isomers)
same chemical formula, different conformation