Gases and the Kinetic-Molecular Theory

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This flashcard set covers the fundamental concepts of gas behavior, the descriptive gas laws (Boyle, Charles, Amontons, Avogadro), the Ideal Gas Law, partial pressures, stoichiometry of gases, and the Kinetic-Molecular Theory.

Last updated 4:54 PM on 5/22/26
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27 Terms

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Pascal (Pa)

The S.I. unit of pressure, where 1Pa=1N/m21\,Pa = 1\,N/m^2.

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Atmosphere (atm)

A unit of pressure defined as 101.325kPa101.325\,kPa, or exactly 760torr760\,torr.

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Barometer

A device used to measure atmospheric pressure, often using a column of mercury.

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Manometer

An instrument used to measure the pressure of a gas in a laboratory experiment, categorized into closed-end and open-end types.

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Boyle’s Law

The law stating that at constant temperature, the volume occupied by a definite mass of gas is inversely proportional to the applied pressure (PV=KPV = K).

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Charles’s Law

The law stating that the volume of a gas sample varies directly with its absolute temperature if the pressure is held constant (VT=K\frac{V}{T} = K).

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Absolute Zero

The theoretical temperature at which a gas would have zero volume, corresponding to 273.15C-273.15^{\circ}C or 0K0\,K.

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Amontons’s Law

The gas law stating that pressure is directly proportional to absolute temperature when volume and amount of gas are held constant (PT=K\frac{P}{T} = K).

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Standard Molar Volume

The volume occupied by 1mol1\,mol of an ideal gas at Standard Temperature and Pressure (STP), which is 22.4L22.4\,L.

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Standard Temperature and Pressure (STP)

A reference condition for gas measurements defined as 0C0^{\circ}C (273.15K273.15\,K) and 1atm1\,atm (760torr760\,torr).

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Ideal Gas Law

The mathematical relationship between pressure, volume, temperature, and number of moles of a gas expressed as PV=nRTPV = nRT.

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Universal Gas Constant (R)

The proportionality constant in the ideal gas law, valued at 0.0821atmLmol1K10.0821\,atm\cdot L\,mol^{-1}\cdot K^{-1} for pressure-volume calculations or 8.314Jmol1K18.314\,J\,mol^{-1}\cdot K^{-1} for energy-related calculations.

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Gas Density (dd)

A property calculated as the mass per unit volume (d=mVd = \frac{m}{V}), which is directly proportional to the molar mass and pressure of the gas.

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Dumas Method

An experimental procedure used to determine the molar mass of a volatile liquid by measuring the mass, volume, temperature, and pressure of its vapor state.

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Dalton’s Law of Partial Pressures

The law stating that the total pressure of a mixture of nonreacting gases is the sum of the partial pressures of the individual gases (Ptotal=P1+P2+P3+...P_{total} = P_1 + P_2 + P_3 + ...).

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Mole Fraction (χ\chi)

A dimensionless quantity representing the ratio of the number of moles of one component to the total number of moles in a mixture (χ1=n1ntotal\chi_1 = \frac{n_1}{n_{total}}).

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Vapor Pressure

The pressure exerted by a vapor in equilibrium with its liquid phase at a given temperature, relevant when collecting a water-insoluble gas over water.

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Kinetic-Molecular Theory (KMT)

A model describing gas behavior based on the postulates that particles have mass but negligible volume, are in constant random motion, and undergo elastic collisions.

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Elastic Collisions

Collisions in which the total kinetic energy of the particles is conserved, meaning no energy is lost as heat or other forms.

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Root-Mean-Square Speed (urmsu_{rms})

A measure of the average speed of gas particles at a specific temperature, defined by the formula urms=3RTMu_{rms} = \sqrt{\frac{3RT}{M}}.

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Effusion

The process by which a gas escapes from its container through a tiny hole into an evacuated space.

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Graham’s Law of Effusion

The law stating that the rate of effusion of a gas is inversely related to the square root of its molar mass.

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Diffusion

The movement of one gas through another due to the random motion of particles.

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Mean Free Path

The average distance a gas molecule travels between successive collisions.

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Collision Frequency

The number of collisions per unit time, obtained by dividing the most probable speed by the mean free path.

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Real Gas

A gas that deviates from ideal behavior because its molecules have finite volumes and exert intermolecular forces on each other.

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Van der Waals Equation

An equation for real gases that adjusts the ideal gas law for molecular volume (constant bb) and intermolecular attractions (constant aa).