GChem Flashcards

(69 cards)

1
Q

Equavalance point

A
  • weak acid+strong base=equlvalence point above 7
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2
Q

PH calculation

A
  • A quick trick to find pH if you’re given [H+] is to take the exponent, and subtract it by 0. (whatever the first number is).
  • So if you’re given H+ = 4.9 x 10^-5, the pH is 5 - 0.4 = 4.6
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3
Q

Handerson Hasselbalch Equation

A
  • Calculate the pH of a buffer
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4
Q

Increasing surface area increase BP

A
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5
Q

IM and BP

A
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6
Q

the different derivatives for the gas laws (and their names)

A

So, the ideal gas law is PV=nRT.

Boyle- Sound similar to “boil” which makes me think of temperature so T is constant. “n” is constant. so P1V1=P2V2

Gay-lussac- I just imagine a sack filled with water and that makes me think of volume so V is constant. “n” is constant so P1/T1=P2/T2

Charles- Lol, I have a friend named Charles so I just think of him with a P shaped scar on his forehead kind of like Harry Potter so P is constant. Idk, it sticks lol. “n” is constant so V1/T1=V2/T2.

Avogadro- I think of Avogadro’s number and this is the only time “n’ is not constant. T is constant so (n1/V1)=(n2/V2)

Just another way of thinking about them. I used to get these mixed up so I had to find a way to think about them haha.

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7
Q

Ea-activation energy

A
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8
Q

Spontaneous rxn and entropy

A
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9
Q

Reaction rate law

A
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10
Q

Gibbs free energy

A
  • The amount of energy in a substance that can be used for work or chemical reactions
  • Available energy
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11
Q

Vapor pressuren (VP)

A
  • a measure of the tendency of a material to change into the gaseous or vapour state, and it increases with temperature
  • BP is when VP=atmospheic pressure
  • High VP= highly volatile= easily evaporate–> doesn’t like high Temperature–>lower BP
  • Higher atmospheric pressure–>lower BP (high pressure cooker)
  • (a higher atmospheric pressure indicates a higher percentage of gas molecules that are not the compound of interest. For instance, in a water and air system, a high pressure indicates that there are more molecules of air (or the molecules are moving faster). This means that in order for the water to want to turn into the vapor phase, more heat will be needed to overcome this high pressure. This leads to an elevated boiling point. The opposite is also true, as decreasing pressure indicates less molecules of air (or slower velocity), thus indicating a lower boiling point)
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12
Q

Solutes

A

* Adding Non-volatile solutes–>decrease VP
–>increase BP
*
* Solutes disrupt overall bonding between solvent liquids. This prevents solutes from escaping as easily but also prevents it from solidifying since the 3d lattice structure of solids is disrupted (ie ice)–>increase BP temperature

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13
Q

Summary of periodic table trends

A
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14
Q

Gibbs Free energy-the energy within the system to do the work

A
  • ΔG =0 if Keq = Q because at equilibrium there is a dynamic halt of net changes in energy or composition; forward rate=backward rate
  • Q < Keq: ∆G < 0: forward reaction has not reached equilibrium: [Reactants] > [products]
    Forward reaction rate increases to restore equilibrium
  • Q > Keq: ∆G > 0: forward reaction has exceeded equilibrium: [Products] > [reactants], Reverse reaction rate increases to restore equilibrium
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15
Q

Another form of Gibbs free energy

A
  • important to understand each individual variable and to simplify the question stem.
    * constants (8.314 J/mol*K)
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16
Q

Why does inductive effect make molecules more acidic?

A
  • when an electronegative atom is attached to a molecule, it pulls electron density away from the acidic hydrogen, making the hydrogen more positive and therefore easier to donate, thus increasing the acidity of the molecule
  • Acids are electron acceptors(proton donors)
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17
Q

differences between nucleophilicity and basicity

A
  • Nucleophilicity involves the ability of a species to attack an electrophile, which is determined by how quickly the attack occurs (kinetics).
  • Basicity, on the other hand, is about the stability of the protonated species once the proton is transferred (thermodynamics)
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18
Q

Thermodynamics

A
  • Acidity/basicity is a measure of thermodynamics and where the equilibrium and Keq will land
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19
Q

OIL RIG

A

Oxidation is loss of electrons=more positive=less negative

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20
Q

IR spectroscopy

A
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21
Q

bicarbonate ion

A
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22
Q

Electrolytic Cell vs. Galvanic (Voltaic) Cell

A
  • **always true:
  • e- from anode to cathode (ox–>cat)**
    ***Oxidation at anode, reduction at cathode
    “An OX, Red Cat” **
    → Anode = Oxidation, Cathode = Reduction (applies to both).
  • Galvanic: “Good” (spontaneous, energy-producing)
  • Electrolytic: “Endothermic” (requires energy input)
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23
Q

standard cell potential

A
  • If free energy negative, then E cell positive
  • signs are opposite
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24
Q

Faraday’s constant

A
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25
hydronium ion
26
balancing a redox reaction
* half reactions * then Balance the changes in electrons directly
27
always soluble
Always soluble: nitrate (NO3-), ammonium, all alkali metals (group 1).
28
(Almost) Always insoluble
* carbonate, phosphate, silver, mercury, lead. All of these, unless paired with something from the “always soluble” list, are insoluble
29
Isoelectric point focusing
30
molarity vs molality
* Molarity-mole/L * Molality-mole/kg
31
calcium sulfate
CaSO4
32
sulfite
SO3 2-
33
polyatomic ions
* The ion with the lesser charge will use the suffix “-ous,” and the ion with the greater charge will use the suffix “-ic.” * For example, the iron (II) cation, Fe2+, is termed the ferrous ion, while the iron (III) cation, Fe3+, is the ferric ion. Monatomic ions use the suffix -ide, as in hydride (H−) or oxide (O2−).
34
oxyanions
-ite O2 -ate O3
35
alpha decay
36
beta-decay
37
beta positive decay
38
size of cations
* cations-smaller ionic radii than the atomic radii (lose electrons) * anions-bigger than the atomic radii
39
Acetone
40
**Hybridization & Bond angels**
41
LiAlH4
If Pd and H2 used, alkene will be touched
42
second law of thermodynamics
* the total entropy (disorder) of an isolated system will always increase over time. * explains why heat flows from hot to cold, why energy transformations are inefficient, and why perpetual motion machines are impossible.
43
solubility constant Ksp
* how much of a solid can dissolve in water to form a solution * High Ksp → More soluble (more ions dissolve)
44
NaOH
Sodium hydroxide
45
indicator
The pH at which a color change is observed during titration depends on the pKa of the indicator (HIn), not the concentration of the weak acid being titrated.
46
1 faraday
=1 mole
47
Boiling Point
* when enough heat has been applied to overcome the intermolecular forces
48
ideal vs. real gas behavior
* when high pressure-gas molecules are forced together-->their own V becomes significant-->**the real volume is greater than predicted by the ideal gas law**
49
good insulator
* has electrons, but not free to move
50
Orbital Order
* How to Spot an Excited State? * If an electron appears in a higher-energy orbital earlier than expected, the atom is in an excited state.
51
periodic table
52
electron affinity
=actual energy gained when adding an electron.
53
isoelectronic
* Different atoms or ions that have the same number of electrons
54
vaccum distillation
* vaccum distillation=reduced pressure * leak will undo vaccum effect
55
dipole moments
* a measure of the separation of charge in a molecule due to differences in electronegativity between atoms * a large difference in electron distribution=high dipole moments
56
electron configuration
57
triple bond
* great strength * very stable and hard to break apart
58
conjugate acid/base
59
ionization potential
* the energy required to remove electrons
60
electron affinity
* the ability of an atom to accept an electron
61
single replacement rxn
62
H2S
* weak acid, have a lower Ka
63
VSEPR
64
Lewis acid/base
* Acid: accept e- * Base: donate e-
65
Bronsted acid/base
* acid: donate H+ * base: accept H+
66
PPM
* parts per million
67
bond strength
* ionic > covalent > hydrogen
68
basic a.a.
HIS LYS ARE-basic
69
acidic a.a.
acids cause **DE**ath