Section 1

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chemical thermodynamics

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Cards (56)

Section 1

(50 cards)

chemical thermodynamics

Front

the area of chemistry that deals with energy relationships

Back

Enthalpy of reaction

Front

heat of reaction

Back

vibrational motion

Front

the atoms in the molecule move periodically toward and away from one another

Back

Exothermic

Front

Releases heat

Back

Fuel Value

Front

the energy released when one gram of any substance is combusted

Back

Enthalpy

Front

heat; internal energy plus the product of pressure and volume

Back

Standard enthalpy change

Front

The total heat produced or absorbed by a system when reactants in their standard states change to products in their standard states under STP conditions.

Back

Renewable energy sources

Front

Are resources that can be replaced in a relatively short amount of time. This includes: hydroelectric, solar, geothermal, wind, biomass, and possibly nuclear fusion.

Back

number of degrees of freedom

Front

forms of motion available to the atoms

Back

Pressure-Volume work

Front

the work involved in the expansion or compression of a gas

Back

first law of thermodynamics

Front

energy is conserved

Back

rotational motion

Front

the molecule spins about an axis

Back

Molar Heat capacity

Front

Heat capacity per mol of substance

Back

First Law of Thermodynamics

Front

Sum of all Kinetic and Potential energies of the components of the system

Back

ideal engine

Front

an engine with the highest possible efficiency

Back

entropy

Front

the extent of randomness in a system or the extent to which energy is distributed among the various motions of the molecules of the system

Back

Joule

Front

SI unit for energy

Back

Bomb calorimeter

Front

measures caloric content of biological materials (sample is burned, heat released)

Back

dispersion of energy

Front

caused by an entropy increase which increases the number of ways the positions and energies of the molecules can be distributed throughout the system

Back

irreversible process

Front

a process that cannot simply be reversed to restore the system and its surroundings to their original states

Back

Calorie

Front

energy required to raise the temperature of 1 gram of water from 14.5 degrees Celsius to 15.5 degrees Celsuis i calorie = 4.184 joules

Back

Enthalpy of formation

Front

the enthalpy change for a reaction in which one mole of a compound is formed from its elements in their standard states

Back

Standard enthalpy of formation

Front

The change in Enthalpy that accompanies the formation of 1 mole of a compound from its elements with all substances in their standard states.

Back

Specific heat

Front

Amount of heat required to raise one gram of a substance by 1 degree Celsius or Kelvin; heat capacity.

Back

broader distribution

Front

the higher the temperature, the faster the molecules move and the more kinetic energy they possess, the hotter the system, the more broader distribution of molecular speeds

Back

Fossil Fuels

Front

A hydrocarbon deposit, such as petroleum, coal, or natural gas, derived from living matter of a previous geologic time and used for fuel.

Back

isothermal process

Front

the expansion of an ideal gas at constant temperature

Back

translational motion

Front

the entire molecule can move in one direction, which is the simple motion we visualize for an ideal particle and see in a macroscopic object like a thrown baseball

Back

Energy

Front

the capacity to do work or transfer heat

Back

statistical thermodynamics

Front

uses the tools of statistics and probability to link the microscopic and macroscopic worlds

Back

second law of thermodynamics

Front

any irreversible process results in an increase in the entropy of the universe, whereas any reversible process results in no change in the entropy of the universe

Back

Work

Front

energy used to cause an object to move against a force

Back

spontaneous process

Front

a process that proceeds on its own without any outside assistance

Back

ThermoChemistry

Front

relationships between chemical reactions and energy changes that involve heat

Back

Endothermic

Front

Absorbs heat

Back

state functions

Front

properties that define a state and do not depend on how we reach that state examples: temperature, internal energy, and enthalpy

Back

State Function

Front

a property of a system that is determined by specifying the systems conditions

Back

Kinetic Energy

Front

energy of motion

Back

Standard State

Front

The standard thermodynamic conditions (often 1 atm or 1 bar and 25 degrees Celsius) chosen for substances when listing or comparing thermodynamic date.

Back

microstate

Front

a single possible arrangement of the positions and kinetic energies of the molecules when the molecules are in a specific thermodynamic state

Back

Calorimeter

Front

an insulated device used to measure the absorption or release of heat in chemical or physical processes

Back

Heat

Front

energy used to cause the temperature of a system to fluctuate

Back

Heat capacity

Front

The amount of energy needed to raise the temperature of substance by one degree Celsius or Kelvin

Back

Calorimetry

Front

The measurement of heat flow (into or out of a system) as the result of a chemical reaction or physical process.

Back

reversible process

Front

a specific way in which a system changes its state, the system can be restored to its original condition with no net change to either the system or its surroundings

Back

nonspontaneous process

Front

the reverse of any spontaneous process

Back

System

Front

the reaction being observed

Back

Thermodynamics

Front

The study of energy and its transformations

Back

Surroundings

Front

everything that is not directly involved in the chemical reaction taking place. i.e: a thermometer measuring the temperature change of an exothermic neutralization between HCl and NaOH

Back

Potential Energy

Front

energy stored

Back

Section 2

(6 cards)

standard molar entropies

Front

molar entropies for substances in their standard states

Back

absolute value of the entropy

Front

determined by experimental measurements and represented by the variable 'S'

Back

standard free energies of formation

Front

the free-energy change for its formation from its elements under standard conditions

Back

standard enthalpies of formation

Front

the enthalpy change when a substance is formed from its elements under defined standard conditions

Back

Gibbs free energy

Front

a state function developed by J. Willard Gibbs, represented by G = H -TS, where T equals the absolute temperature

Back

third law of thermodynamics

Front

the entropy of a pure, perfect crystalline substance at absolute zero is 0

Back