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100
The conjugate base of CH3COOH (Name AND formula)

CH3COO-; Acetate

100

Name a weak acid, ANY weak acid, and its conjugate base

examples:

acetic acid -> acetate

formic acid -> formate

phosphoric acid -> dihydrogen phosphate

water -> hydroxide

100

A stronger acid/base will have a ________ Ka or Kb value respectively

HIGHER/GREATER/LARGER/INCREASED/etc...

100

The conjugate acid of hydrogen sulfate is ______

The conjugate base of hydrogen sulfate is ______

CA: Sulfuric Acid H2SO4

CB: Sulfate SO42-

100

The formula that relates pH and pOH

14 = pH + pOH

200

A _________ is a substance that produced hydroxide ions in water

Arrhenius Base

200

The formula for pH, given proton concentration, is ________

pH = -log([H+])
200

A ________ is a substance that accepts a lone pair of electrons

Lewis Acid

200

A _______ pKa indicates a stronger acid

lower

200

A ________ is a substance that donates protons

Bronsted-Lowry Acid

(Not Arrhenius, as that is specifically in WATER)

300

The formula that relates Ka and Kb

Kw = (Ka)(Kb)

300

Hydroxides made of alkali and alkaline earth metals are strong bases except for those made with ____ and ____

Beryllium and Magnesium

300

NaCH3COO is a(n) ________ salt

Basic

Na came from NaOH (strong base)

CH3COO came from CH3COOH (weak acid)

300

The pH of 0.005 M HCl

-log(0.005)

pH = 2.3

300

50 mL of 0.5 acetic acid is titrated with 0.125 sodium hydroxide. The Kb of acetic acid is 5.6 x 10-10. What is the pH at half-equivalence?

pH = pKa (at half equivalence)

pH = -log(Ka) = -log(Kw/Kb)

pH = -log(1.8 x 10-5) = 4.74

400
Methylamine (CH3NH2) acts as base. When 0.125 M is placed in water, what is the equilibrium pH? (Ka = 2.273 x 10-11)

Kb = Kw/Ka = 4.4 x 10-4

(ICE TABLE, then...)

x = sqrt(0.125*4.4*10-4)

x = [OH-] = 0.00742

pH = 14-pOH = 14+log(0.00742) = 11.87

400

0.03 M Phosphoric acid (first proton pKa is 2.13) is placed into water. The percent ionization is _____

H3PO4 -> H+ + H2PO4-

Ka = 10-pKa = 7.41 x 10-3

7.41 x 10-3 = ([H+][H2PO4-)/([H3PO4])

= (x2)/(0.03-x)

x = 0.0115

% = (0.0115/0.03) x 100 = 38.3% ionization

400

I have a beaker with 0.2 M ammonium and 0.150 M ammonia (Kb of ammonia is 1.8 x 10-5). The pH of this system is _______

Hint: There is an easy way, and there is a hard way (ICE table is the hard way)

The easy way:

pH = pKa + log(A-/HA)

= -log(Kw/Kb) + log(0.15/0.2)

= 9.25 - 0.125

pH = 9.12

400

The seven strong acids are:

Hydroiodic: HI

Hydrobromic: HBr

Hydrochloric: HCl

Perchloric: HClO4

Chloric: HClO3

Nitric: HNO3

Sulfuric (first proton): H2SO4

400

Mg3(PO4)2 is a _______ salt

HINT:

Mg(OH)2 has a pKb of 10.91

H3PO4 has a pKa of 2.15

Acidic salt

Phosphoric acid is a stronger acid than magnesium hydroxide is a base

The acid is stronger than the base

500

A buffer with a Ka of 1.202 x 10-5 has a pH of 4.6. The buffer ratio is...

pH = pKa + log(A-/HA)

4.6 = -log(1.202 x 10-5) + log(buffer ratio)

4.6 = 4.92 + log(buffer ratio)

-0.32 = log(buffer ratio)

buffer ratio = 10-0.32

Ratio = 0.4786

500

A buffer has a pH of 11.2, and contains 0.51 M of the conjugate acid and 0.49 M of the conjugate base. What is the Ka of the buffer?

pH = pKa + log(CB/CA)

11.2 = -log(Ka) + log(0.49/0.51)

11.217374 = -log(Ka)

Ka = 10^(-11.217374)

Ka = 6.06 x 10-12

500

This value is the pH of a solution where [H+] is 10,000 times less than [OH-]

[H+] = [OH-]/10,000

Kw = [H+][OH-]

Kw = ([OH-]/10,000)*([OH-])

[OH-] = sqrt(Kw * 10,000) = 0.00001

pOH = -log(0.00001) = 5

pH = 14 - pOH = 9

500

My buffer is 1 L, and has 0.15 M acetate and 0.2M acetic acid (Ka = 1.8 x 10-5). I drop in 0.04 moles of hydrochloric acid. What is the new pH?

CH3COO- (aq) + H3O+ (aq) --> CH3COOH (aq) + H2O

Moles of acetate: 0.150-0.04 = 0.11 moles = 0.11M

Moles of acetic acid: 0.2 + 0.04 = 0.24 moles = 0.24M

Hydrochloric acid: 0.04 - 0.04 = 0 moles

pH = pKa + log(A-/HA)

pH = -log(1.8x10-5)+log(0.11/0.24)

pH = 4.4

500

0.5 M sulfuric acid is placed in water (Ka of second proton is 1.2 x 10-2). What is the equilibrium pH? 

Note: Consider the dissociation of the first AND second proton

First proton is strong, so we end up with 0.5 M hydrogen sulfate and 0.5 M protons. Set up ICE table, and you get Ka = ((0.5+x)(x))/(0.5-x)

x = 0.012 = [H+] after second dissociation

First + second dissociations = 0.5 + 0.012 = 0.512

pH = -log(0.512) = 0.291

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