Module 1 and 2 Flashcards

1
Q

K > Q which reaction is favoured

A

Forward

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

K < Q which reaction is favoured

A

Backward

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Will a precipitate form if Q > K

A

Yes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Will a precipitate form if Q < K

A

No

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

The stronger the acid or base, the _____ the conjugate

A

Weaker

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Ligands act as

A

Lewis bases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Acid base reactions involve the exchange of

A

1 proton

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Redox reactions involve the exchange of

A

Electrons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

“X is titrated with Y” (where are these solutions located)

A

X in flask (unknown concentration), Y in burette (known concentration)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Ratio of buffer made with weak acid or base and conjugate

A

1:1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Ratio of buffer made with weak acid/base and strong acid/base

A

2:1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Ionisation status depends on

A

pH of solution and pKa of functional group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Percent protonated when >1 unit below pKa

A

90%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Percent deprotonated when >1 unit above pKa

A

90%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Amino acid pKa below which all are protonated

A

2.5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Amino acid pKa above which all are deprotonated

A

9.5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

𝚫fH

A

change in enthalpy for the formation of 1 mole of a compound from its constituent elements in their standard states (already in standard states= 0)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

𝚫vapH

A

change in enthalpy for one mole of a substance changing from a liquid to a gas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

𝚫fusH

A

change in enthalpy for one mole of a substance changing from a solid to a liquid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

𝚫comH

A

change in enthalpy for the combustion of one mole of a substance in oxygen (products CO2, H2O)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Negative change in enthalpy

A

Exothermic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Positive change in enthalpy

A

Endothermic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Spontaneous meaning

A

Once started continues without help, not necessarily to completion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Standard entropy conditions

A

1molL^-1, 1 bar pressure, no value for temperature

25
Positive Gibbs energy
Non spontaneous under standard conditions
26
Negative Gibbs energy
Spontaneous under standard conditions
27
Gibbs energy = 0
Equilibrium
28
What does the magnitude of G tell us
How far a reaction will go to completion (no absolute value of G)
29
𝚫fG for a pure element
0
30
Units for enthalpy
kJmol^-1
31
Units for entropy
JK^-1mol^-1
32
Positive enthalpy and entropy
Spontaneous at high temperatures
33
Negative entropy, negative enthalpy
Spontaneous at low temperatures
34
Positive entropy, negative enthalpy
Spontaneous at all temperatures
35
Negative entropy, positive enthalpy
Non spontaneous at all temperatures
36
Units of k 0th order
molL^-1s^-1
37
Units of k 1st order
s^-1
38
Units of k 2nd order
Lmol^-1s^-1
39
Units of k 3rd order
L^2mol^-2s^-1
40
What is a pseudo first order reaction
[B] >> [A], when [B] changes [A] doesn't change much
41
Unit for rate
molL^-1s^-1
42
What is Ea
Energy difference between reactant and highest energy transition state
43
Straight line Arrhenius equation rearrangement
lnk = -Ea/R 1/T + lnA
44
When can you use the integrated rate law
Only for first order reactions
45
The rate doubles for every ___ increase in temperature
10C
46
E standard will always be _____ for a spontaneous reaction
Positive
47
The smaller the Ka or Kb, the _____ the acid or base
Weaker
48
The larger the pKa or pKb, the _____ the acid or base
Weaker
49
The larger the Ka or Kb, the _____ the acid or base
Stronger
50
The smaller the pKa or pKb, the _____ the acid or base
Stronger
51
Ligand definition
Molecule or ion in which one or more donor atoms have a lone pair of electrons (biologically important donor atoms: N, O, P, S) (an ion or molecule attached to a metal atom by coordinate bonding.)
52
Ligands act as
Lewis bases (donate electrons to transitional metal ion)
53
When water is the ligand, resulting complex can act as
Weak base
54
Ligand complex becomes more acidic as
Charge on cation increases
55
What doesn't appear in Kc expressions
Pure solids AND liquids
56
The _____ the acid or base, the ______ the conjugate
Stronger, weaker
57
Straight line axes for linear first order reaction
ln[X] vs t
58
Arrhenius equation
K = Ae^-Ea/RT