Exam Four Flashcards
bronsted and lowry definitions of acids and bases
ACIDS: release a H+
BASES: accept H+
keq/ the equilibrium constant
aA + bB = cC + dD
Keq = [C]c[D]d/ [A]a[B]b
products/reactants
- solids and solvents are omitted
keq > 1 (reactants are favored)
keq < 1 (products are favored)
keq = 1 (reactants = products)
le chatelier’s principle
when a reversible reaction is pushed out of equilbrium, the reaction responds to reach a new equilibrium
- any changes in conc. pressure or temp can be a disruption
- RATE OF FORWARD REACTION INCREASES (addition to the reaction)
- RATE OF REVERSE REACTION INCREASES (removal from reaction)
the equilibrium constant of water
Kw = 1.0 x 10^-14
a solution with a higher H3O+ than OH- will be:
have a pH lower than 7, and be acidic
pH scale
acidic pH < 7
neutral pH = 7
basic pH > 7
acid and base strength
STRONGER THE ACID - more H3O+ PRODUCTION - LOWER PH
STRONGER THE BASE - more OH- - HIGHER PH
LARGER KA - STRONGER ACID
LOWER PKA - STRONGER ACID
neutralization
- occurs when an acid and a base react to form a salt and water
- reaction seen when proper amounts of acid and base are added
titration
- lab technique used to determine conc. of an acid and base solution
- acid solution (unknown), base of known conc. is ADDED to consume acid
- specific indicator added to find titration end point
buffers
- solution that is resistant to a pH change when a small amount of acid or base is added
- created from weak acid and conjugate base; are within a 50:50 ratio
- most resistant to pH changes when the pH is equal to pKa of the acid
carbohydrates
- can be seen through sugars and starches
- help provide energy
- used to store energy
- plants produce them through photosynthesis
- stored carbs can be broken down to produce energy
monosaccharides
classified by their functional group
- aldoses - contains aldehyde
- ketoses - contains ketone
chiral C atom
one that is attached to 4 different atoms or groups of atoms
D or L sugars
D sugars: -OH attached to the chiral carbon FURTHEST FROM CARBONYL GROUP to the RIGHT
L sugars: -OH attached to the LEFT
amino sugars
an -OH group of a monosaccharide has been replaced by an amino (-NH2) group