Unit 4 + Gas Laws Test

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Gas Laws, Kinetic Molecular Theory, Deviation from Ideal Gas Law, Titrations, Redox Reactions, Stoichiometry, Acid-Base Reactions

Last updated 12:00 PM on 10/8/25
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35 Terms

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Boyle’s Law

P1V1=P2V2

  • Pressure and Volume are Inversely Related

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Charles’ Law

V1/T1=V2/T2

  • Volume and Temperature are directly related

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Gay-Lussac’s Law

P1/T1=P2/T2

  • Pressure and Temperature are directly proportional

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Avagadro’s Law

V1/n1=V2/n2

  • Volume and number of moles are directly related

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Ideal Gas Law

PV=nRT

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Combined Gas Law

P1V1/n1T1=P2V2/n2T2

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Derivation Ideal Gas Law

MM = DRT/P

D = MMP/RT

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Mole Fraction

XA = nA / nA+nB

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Partial Pressure

Pgas=Xgas(Ptotal)

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Kinetic Molecular Theory

  1. The particles are so small compared with the distance between them that the volume of individual particles can be assume to be negligible

  2. Particles are in constant, random motion

  3. Particles are assumed to exert no force on each other; they are assumed neither to attract nor to repel each other

  4. Average kinetic energy of gas particles is assumed to be directly proportional to the Kelvin temperature of the gas

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Kinetic Energy

KE = 1/2mv2

  • Kinetic energy is the energy that objects possess due to their motion

  • Gases at the same temperature have the same average kinetic energy

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Partial Pressure

Ptotal = P1 + P2 + P3 + …

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Diffusion

The spread of one substance throughout a space or throughout a second substance

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Effusion

The escape of gas molecules through a tiny hole into an evacuated space

Rate of effusion depends on the mass of the gas

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Graham’s Law

V1/V2 = sqrt(m2/m1)

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Correct for non-ideal gas behavior when..

  • Pressure of the gas is high → actual observed pressure of the gas is lower than expected pressure due to intermolecular attractions

  • Temperature is low → Actual observed volume of the gas particles is higher than expected due to gas particles actually taking up space

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van der Waals Equation

(P + an2/V2)(V - nb) = nRT

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Analyte

Solution with unknown molarity

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Equivalence Point

The point in the titration when enough titrant has been added to react exactly with the substance in solution being titrated related by the role ratio in balanced reaction

Seen through the inflection point on a titration curve

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End pont

When the indicator changes color

Not necessarily the same as the end point, but ideally they are as close as possible

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Oxidation

Increase in oxidation state (loss of electrons)

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Reduction

Decrease in oxidation state (gain of electrons)

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Oxidizing Agent

Reactant that causes oxidation (reactant with the element being reduced)

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Reducing Agent

Reactant that causes reduction (reactant with the element being oxidized)

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Arrhenius Acid

Any species that produced H+/H3O+ in solution-

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Arrhenius Base

Any species that produced OH- in solutio

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Bronsted-Lowry Acid

Acids are proton donors

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Bronsted-Lowry Base

Bases are proton acceptors

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Conjugate base

The acid molecule that lost one proton

Becomes more negative

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Conjugate acid

The base molecule that gained one proton

Becomes more positive

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Strong Acids and Bases

Completely ionizes in water

Reaction goes to completion

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7 Strong Acids

HCl

HBr

HI

HNO3

HClO3

HClO4

H2SO4

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8 Strong Bases

LiOH

NaOH

KOH

RbOH

CsOH

Ca(OH)2

Sr(OH)2

Ba(OH)2

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Weak Acids and Bases

Partially ionizes in water

Weak acids and bases stay together in chemical equations

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An acid-base reaction will favor the formation of the ____ conjugate acid and base

weaker

  • Stronger acid will form a weaker conjugate base

  • Stronger base will form a weaker conjugate acid