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1 C
meth (methane)
2 C
eth (ethane)
3 C
prop (propane)
4 C
but (butane)
5 C
pent (pentane)
6 C
hex (hexane)
7 C
hept (heptane)
8 C
oct (octane)
9 C
non (nonane)
10 C
dec (decane)
11 C
undec (undecane)
12 C
dodec (dodecane)
1 C in Sub
methyl
2 C in Sub
ethyl
3 C in Sub
propyl
4 C in Sub
butyl
5 C in Sub
pentyl
6 C in Sub
hexyl
7 C in Sub
heptyl
8 C in Sub
octyl
9 C in Sub
nonyl
10 C in Sub
decyl
Branched alkyl group with 3 C
isopropyl (1-methylethyl)
Branches alkyl groups with 4 C
tert-butyl (1, 1-dimethylethyl)
If the parent chain is cyclic…
add the prefix “cyclo”
Prefixes are ignored when…
alphabetizing the substituents
Isomers
different structures, same molecular formula
Constitutional Isomers
different connectivity of atoms
Conformations
single bonds rotate, resulting in multiple 3D shapes
Newman projections
ideal for comparing the relative stability of possible conformations resulting from single bond rotation (focus on specific bond)
Angle between atoms on adjacent carbons
Dihedral angle
Staggered conformations are…
more stable, lower in E
Eclipsed conformations are…
less stable, higher in E
Torsional strain
Reason for difference in energy between the staggered and eclipsed conformations