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stereoisomers
same MF, same atomic connectivity, diff 3D arrangements
why cant you rotate stereoisomers
will break the pi bonds
what makes a molecule capable of having stereoisomers
different atoms on top and bottom of connecting molecule

vinyl

allyl
rules for naming alkenes
principal chain - chain w most double bonds, alkene carbons get lowest #
name for highest priority (largest mass) atom on same size
Z - zusammen “together”
name for highest priority (largest mass) atom on diff sides
E - entgegen “across”
how do you determine E or Z if sides are the same?
compare atom of higher mass, if same continue process
duplication rule
if double bond - add atom to both sides
triplication rule
if triple bonded - add atom to both sides twice
does stability increase or decrease when the amt of R groups increases
increases
does the type of R group matter when considering stability?
no, all the same
why do more R groups make an alkene more stable?
partial positive charges (orbitals) and therefore the induction effect