Exam 2 Flashcards
how to find amt. of stereoisomers present?
2^n
what pka is favored?
higher pka
nucleophile
-negative usually
-usually have lots of lone pairs
acid
-hydrogen bonded to electronegative
-must be positive
-acid stronger if H bonded to more electronegative
-stronger if more resonance can be drawn of negative conjugate base
electrophile
-seek out e-
-basically acid
base
-need a lone pair
-must be negative
-strong if basic atom is more electropositive
-fewer resonance structures, stronger base
what does a higher activation energy mean?
slower
exergonic
releases energy
always spontaneous
endergonic
gains energy
always nonspontaneous
G is always negative if…
negative H
positive S
G is always positive if…
positive H
negative S
G is probably negative if…
negative H
negative S
G is probably positive if…
positive H
positive S
K>1
G neg
exergonic
K=0
G= 0
K<1
G positive
endergonic
Acid Base rxn
A proton (H+) is transferred from one molecule to another
Addition
-pi bond broken
-new sigma bond forms to each of the two atoms formerly involved in the pi bond
Elimination
-pi bond forms
-2 sigma bonds break
Substitution
Sigma bond to an atom breaks but new sigma bond to that atom forms
Rearrangement
A new isomer of a molecule is formed
Rearrangement
A new isomer of a molecule is formed