Exam 2 Flashcards

1
Q

conjugate base

A

species that remains when a proton has been removed from an acid

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2
Q

Conjugate acid

A

species that forms when attaches to a base

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3
Q

Arrhenius and bronsted lowry acid/base definitions

A

Arrhenius: Acids yield H+ and bases yield OH-

Bronsted-lowry: acids donate H+ and bases accept H+

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4
Q

Relationship between Kw and temp

A

direct

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5
Q

Formula for how many times faster a reaction is with a catalyst or for change in Ea

A

ln(k1/k2)=(Ea1-Ea2)/RT

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6
Q

How is pH of polyprotic acids determined?

A

The Ka of the first step determines the pH except for H2SO4.
For H2SO4: Write the first step and use stoichiometry to calculate the initial concentrations of HSO4-, then plug those into an ice table for the second step of the dissociation. Solve for x using quadratic formula for Ka2

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7
Q

degree of ionization

A

d=|H+| / |HA|i

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8
Q

Factors affecting acid strength

A
  1. Oxygen’s bonded to central atom: O bonded to the central atom draw electron density towards themselves. More electron density drawn away from O-H groups=more delocalized negative charge the anion formed when H+ is lost, more O=stronger
  2. Higher oxidation number of central atom=stronger acid
  3. Higher electronegativity of halogen atom=stronger
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9
Q

Exception to acid strength trends

A

H3PO4 is not stronger than H3PO3 because H3PO3 is diprotic

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10
Q

how do qualitatively determine pH of salts of weak acids and bases

A
  1. pKa=pKa: neutral

2: Ka(acid)>Kb(base)
Ka(conjugate base)>Kb(conjugate acid)
acidic

vice versa=basic

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11
Q

How to know if amphiprotic ions are acidic or basic

A

see if Ka and Kb are higher

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12
Q

Relationship between Q and K

A

Q>K: shift left

Q

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13
Q

Effects of volume on equilibrium

A

Changing volume will change partial pressures, and therefore Q

Indirect relationship with pressure, directly effects pressure

Decrease volume: QK side with more moles

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14
Q

Effects of pressure on equilibrium

A

Increase pressure: decrease volume, go towards side with fewer moles

Decrease pressure; increase volume, go to side with more moles

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15
Q

What is used to prepare buffers?

A
  1. weak acids and their conjugate bases or weak bases and their conjugate acids
  2. weak acid and strong base
  3. weak base and strong acid
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16
Q

Equation for pH of a buffer solution

A

pH=pKa+log(Mf,base/Mf,acid)

or

pH=pKa+log(Mi,base•Vbase/Mi,acid•Vacid)

17
Q

How to find final molarities of the acid and base components of buffers?

A

use M1V1=M2V2

18
Q

Formulas for adding a strong base to a buffer solution

A

Mf,a,buff=(Mia,buff•Vbuff-Mbase•Vbase)/(Vbuf+Vbase)

Mf,b,buff=(Mib,buff•Vbuf+MbaseVbase)/(Vbuf+Vbase)

19
Q

Formulas for adding a strong acid to a buffer solution

A

Mf,a,buff=(Mia,buf•Vbuf+Macid•Vacid)/(Vbuf+Vacid)

Mf,b,buf=(Mib,buf•Vbuf-Macid•Vacid)/(Vbuf+Vacid)

20
Q

Strong acid-Strong base titration

A

Before equivalence point: Ma,f=(MaVa-MbVb)/(Vb+Va)
MaVa>MbVb

At equivalence point: MaVa=MbVb and pH=7

After equivalence point: MaVa

21
Q

Strong base-strong acid titrations

A

Before equivalence point: Mb,f=MbVb>MaVa
Mb,f=(MbVb-MaVa)/(Vb+Va)

At equivalence point: MbVb=MaVa
pH=7

After equivalence point: MbVb

22
Q

formula for change in temp(Arrhenius)

A

ln(k2/k1)=-Ea/R(1/T2-1/T1)

23
Q

Titrating a weak acid with a strong base

A

Before equivalence point: MaVa>MbVb
Ma,f=(MaVa-MbVb)/(Vb+Va)
Mb, f= MbVb/(Vb+Va)
Henderson Hasselbalch can be used

At eq point: MaVa=MbVb(pH>7)
Msalt,f=MaVa/(Va+Vb)=MbVb/(Vb+Va)
equilibrium calculation with kb can be done

After eq point: MaVa

24
Q

Titrating a weak base with a strong acid

A

Before eq point: MbVb>MaVa
Mb,f=(MbVb-MaVa)/(Vb+Va)
Ma,f=MaVa/(Vb+Va)
Henderson hasselbalch can be used

At eq point: MaVa=MbVb(pH<7)
Msalt,f=MaVa/(Vb+Va)=MbVb/(Vb+Va)
Salt hydrolysis: equilibrium calculation with Ka can be done

After eq point: MbVb

25
Q

What happens to pure water as temperature increases?

A

Greater fraction of water molecules ionize as temp increases, and pH decreases