Qbank test 1 Flashcards

1
Q

Rate equation

A

Intermediates are never in the rate law.

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2
Q

Common ion effect

A

Will reduce the solubility of a solid.
Hinders product formation.
(Look up rule later in gen chem notes)

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3
Q

Kinetic Energy of a particle/object

A

KE=1/2m(v^2)

Average KE is only dependent on temp. If molecules are at same temp, they have same KE. (differences in velocity account for mass differences)

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4
Q

Gibbs free energy equation

A

Tells you whether rxn will be spontaneous

G=H - TS

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5
Q

Laws of Thermodynamics

A

(1) Energy is conserved
U=Q-W
(2)Spontaneous rxns create entropy
(3)S=0 when T=0K (absolute zero)

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6
Q

Adiabatic system

A

No heat transfer b/w system and environment.

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7
Q

Removing electrons from d orbital

A

It is easier to remove electrons from the s orbital before removing from the d orbital.

n+l rule*

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8
Q

Ideal gas law

A

PV=nRT

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9
Q

Allotrope

A

Different forms of the SAME element.

If there is any change in the type of atoms “originally” present, it is not an allotrope.

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10
Q

Two major factors that affect chemical rxns

A

Thermodynamics and kinetics.

Need to think about them BOTH when determining why something is happening.

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11
Q

Heterogeneous vs homogeneous catalysis

A

Homo=reactants and catalyst in same state
Gives stable structures despite changes in coord. #

Hetero=reactants and catalyst in different states

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12
Q

Zero, First, Second & Third order rate law

A

Sum of the exponents of the molecules in the rate equation give total order

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13
Q

Oxidation rules

A

(1) Molecules in free form (H2, O2) have 0 oxidation #
(2) Oxidation of a monoatomic ion is its charge
(3) Sum of oxidation #’s in neutral compound is zero
(4) Oxidation # of grp IA=+1 and IIA=+2
(5) Oxidation # of H=+1 unless in binary metal hydride (-H2) where oxidation #= -1
(6) Oxidation # of O= -2; O= -1 in peroxides and O=+1 w/ Fluorine
(7) Oxidation of fluorine is -1; Cl, Br, I = -1 unless w/ F or O

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14
Q

Catalysis

A

Alters the rate of a rxn but NOT it’s equilibrium.

Reduces activation E needed.

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15
Q

Aufbau principle

A

Know how to determine electron configuration.

Fill lowest E orbitals first (build-up)

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16
Q

Formal charge

A

Formal charge=grp# - (lone pairs) - # of bonds

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17
Q

Review Titration curves

A

Equivalence pt=when mols of base equal mols of acid
Buffer regions= areas of small pH change
Polyprotic vs monoprotic (# of pKa’s)

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18
Q

Amphoteric species

A

Compound that can act as an acid or base.

i.e. water

19
Q

Arrhenius acid/base

A

Acid=donates H+ to solution

Base=donates OH- to solution

20
Q

Bronsted Lowry acid/base

A

Acid=proton donor

Base=proton acceptor

21
Q

Lewis acid/base

A

Acid=electron acceptor

Base=electron donor (nucleophiles)

22
Q

Buffers

A

To prevent extreme pH changes.

Common ion effect

23
Q

Know how to interpret phase diagrams

A

Regions of solid, liquid, gas.

Critical pt=where phases can no longer be distinguished

24
Q

Hydrogen bonding

A

-FH, -OH, -NH

Increases melting pt and boiling pt

25
Q

Lattice energy

A

Generally decreases when either the cation OR anion increases in size.
Will not matter if both cation and anion increase in size at the same time.

26
Q

Types of reactions

A
Single displacement
Double displacement
Neutralization (acid/base)
Oxidation/reduction
Precipitation
Combustion (oxygen)
Combination
Disproportionation=opposite of combination
27
Q

Graham’s law of diffusion

A

(v1^2)MM1=(v2^2)MM2

28
Q

Strength of an ionic salt

A

Made of the most electropositive and electronegative elements (metal & nonmetal)

29
Q

Steps of a Free Radical Reaction

Write it out

A

3 steps
Initiation (radical formation)
Propagation (rxn can still go on)
Termination (stops rxn from going on)

30
Q

Oxidation vs reduction

A

Oxidation means becoming positive (losing electrons)

Reduction means becoming negative (gaining electrons)

31
Q

What environment do gases prefer?

A

Increased volume
Low pressure
Higher temp

32
Q

van der Waals equation

A

(P+(n^2 x a)/(V^2)) x (V-nb) = nRT

This equation is used when the gas being described is not ideal (high pressure and low temp)

33
Q

Solubility rules

A

(1) All alkali (IA) salts soluble
(2) All NH4+ salts soluble
(3) All Cl-, Br-, I-soluble EXCEPT Ag+, Pb+, Hg2 2+
(4) All SO4 2- soluble EXCEPT Ca2+, Sr2+, Ba2+, Pb2+
(5) All oxides insoluble EXCEPT CaO, SrO, BaO, alkali
(6) All OH- insoluble EXCEPT Ca2+, Sr2+, Ba2+, alkali
(7) All CO3 2-, PO4 3-, S2-, SO3 2- insoluble EXCEPT alkali, NH4+
(8) All Na+, NO32- salts soluble

34
Q

H+ conc. and pH equation

A

pH= -log [H+]

35
Q

Osmotic pressure equation

A

osmotic pressure (pi symbol thing) = MRT

R=0.0821

36
Q

Electrolysis equation

A

mass of material = it/nF x formula weight of material

n=moles of electrons transferred

37
Q

Avogadro’s volume

A

at STP = 22.4 L/mol

38
Q

Know how to balance half reactions

A

Will not always get the reaction in the passage.

This affects the moles of electrons you are dealing with

39
Q

Charge density

A

First determined by the charge an ion does or does not have.

If two ions have same charge then whichever is smaller (hold electrons more tightly) will have greater charge density.

40
Q

Heating curves

A

Review them.

Slope=change in T/q

41
Q

Ksp

A

Increases with increased temperature (generally)

42
Q

STP

A

1 atm
0 C or 273 K
22.4 L/mol

43
Q

Vibrational frequency of bonds

A

Depends on the masses of atoms involved (m) and the bond strength (k)

f=(1/2pi) x sqrt(k/m)