Ch2 Flashcards
(28 cards)
Bronsted- Lowry acid
loses a proton
Bronsted- Lowry Base
gains a proton
conjugate base
짝염기
conjugate acid
짝산
Ka
acid dissociation constant/ K(eq) [H2O]
pKa
-log Ka
__________ the acid , lower the _____ Value
stronger, pKa
pH
-log [H+]
Carboxylic Acid
COOH group
Alcohols
OH group
Amines
compounds that result from replacing one or more of the hydrogens bonded to ammonia with a carbon-containing substituent
Curved arrow always points from the electron_____ to the electron _______
donor acceptor
Protonated alcohols, protonated carboxylic acids, and protonated water have pKa values less than
0
carboxylic acids have pKa values of
~5
Protonated amines have pKa values of
~10
Alcohols and water have pKa values of
~15
In an acid-base reaction, the equilibrium favors the formation of the _____ acid
weaker
pK(eq)
pKa(reactant acid) - pKa (product acid)
sp hybridized orbital is more ____ than sp3
electro negative
the ____ of the atom is more important than its _________ in determining how well it bears its negative charge
size, electronegativity
as a halide ion _____ in size, its stability _____ because its negative charge is spread over a larger volume of space
increase, increase
inductive electron withdrawal
pulling electrons through sigma bonds
the effect a substituent has on the acidity of a compound _____ as the distance between the substituent and the acidic proton increase
decrease
the rationale behind carboxyliic acid being stronger than alcohols
1) Inductive Electron Withdrawal
2) Delocalized Electrons