AP Chemistry Test B

AP Chemistry Test B

For the Stanford OHS AP Chemistry class

memorize.aimemorize.ai (lvl 286)
Thermochemistry

Preview this deck

How do you calculate \(\Delta H_{rxn} \degree\)?

Front

Star 100%
Star 100%
Star 100%
Star 100%
Star 100%

5.0

1 review

5
1
4
0
3
0
2
0
1
0

Active users

2

All-time users

2

Favorites

0

Last updated

6 months ago

Date created

Sep 29, 2020

Cards (48)

Thermochemistry

(48 cards)

How do you calculate \(\Delta H_{rxn} \degree\)?

Front

Subtract the enthalpies of formation of the reactants multiplied by their stoichiometric coefficients from the enthalpies of formation of the products multiplied by their stoichiometric coefficients

Back

If a chemical equation is reversed, what happens to \(\Delta H_{rxn}\)?

Front

It changes sign

Back

Definition of molar heat capacity

Front

Amount of heat required to raise the temperature of 1 mole of a substance by \(1 \degree C\)

Back

Standard state

Front
  • For a Gas: The standard state for a gas is the pure gas at a pressure of exactly 1 atm.
  • For a Liquid or Solid: The standard state for a liquid or solid is the pure substance in its most stable form at a pressure of 1 atm and at the temperature of interest (often taken to be 25 °C).
  • For a Substance in Solution: The standard state for a substance in solution is a concentration of exactly 1 M.
Back

Negative \(\Delta H\)

Front

Exothermic reaction

Back

When energy is transferred to a substance, is \(\Delta E\) positive or negative?

Front

Positive

Back

Standard Enthalpy Change (\(\Delta H \degree\))

Front

The change in enthalpy for a process when all reactants and products are in their standard states. The degree sign indicates standard states.

Back

When a substance is warmed, is \(\Delta E\) positive or negative?

Front

Positive

Back

Definition of heat capacity

Front

Quantity of heat required to change its temperature by \(1 \degree C\)

Back

The amount of energy lost by the system must __ the amount gained by the surroundings

Front

equal

Back

Bomb calorimetry occurs at constant __ and measures __ for a reaction

Front

volume, \(\Delta E\)

Back

Positive \(\Delta H\)

Front

Endothermic reaction

Back

Sign Conventions for \(q\), \(w\), and \(\Delta E\)

Front
Back

If no heat escapes from the calorimeter, the amount of heat gained by the calorimeter __ that released by the reaction

Front

equals

Back

At constant volume, what is \(\Delta V\)?

Front

$$0$$

Back

Definition of specific heat capacity

Front

Amount of heat required to raise the temperature of \(1\) gram of the substance by \(1 \degree C\)

Back

$$E$$

Front

Internal energy - the sum of the kinetic and potential energies of all of the particles that compose the system

Back

Definition of \(\Delta E\)

Front

$$\Delta E = q + w$$

 

Where \(q\) is heat and \(w\) is work.

Back

The standard enthalpy of formation of pure elements in their standard state is __

Front

$$0$$

Back

Standard enthalpies of formation at \(298 K\)

Front
Back

What is \(q_{soln}\)?

Front

The heat absorbed by or lost from the solution (which is acting as the surroundings)

Back

Standard Enthalpy of Formation (\(\Delta H_f \degree\))

Front
  • For a Pure Compound: The change in enthalpy when 1 mol of the compound forms from its constituent elements in their standard states.
  • For a Pure Element in Its Standard State: \(\Delta H_f \degree = 0\).
Back

Relate the heat absorbed, heat capacity, and temperature change of a calorimeter

Front

$$q_{cal} = C_{cal} \cdot \Delta T$$

Back

Hess's law

 

Get \(\Delta H_{rxn}\) for \(A + 2B \rightarrow 2D\) using the equations \(A + 2B \rightarrow C\) and \(C \rightarrow 2D\)

Front
Back

What is \(\Delta H_{rxn}\)?

Front

Enthalpy of reaction or heat of reaction and depends on the amount of material undergoing the reaction

Back

Relate work to external pressure and change in volume

Front

$$w = −P_{ext} \cdot \Delta V$$

Back

Molar heat capacity

Front

$$\frac{J}{\text{mol} \cdot C \degree}$$

Back

Thermal equilibrium

Front

No additional net transfer of heat

Back

Convert from specific heat to molar heat capacity

Front

Multiply by the molar mass (\(\frac{g}{\text{mol}}\))

Back

At constant volume, what is \(w\)?

Front

$$0$$

Back

If a chemical equation is multiplied by some factor, what happens to \(\Delta H_{rxn}\)?

Front

It is also multiplied by the same factor

Back

Define change in enthalpy (\(\Delta H\))

Front

$$\Delta H = \Delta E + P \Delta V = q_p$$

Back

How do we measure the thermal energy exchanged between the reaction (defined as the system) and the surroundings?

Front

We observe the change in temperature of the surroundings

Back

Coffee-cup calorimetry occurs at constant __ and measures __ for a reaction

Front

pressure, \(\Delta H\)

Back

State function

Front

Does not depend on how the system arrived at that state

Back

Define enthalpy (\(H\))

Front

$$H = E + PV$$

Back

When work is done on the surroundings by the system, \(w\) is

Front

negative

Back

When two substances are mixed and allowed to come to thermal equilibrium, what is the relation between their \(q\) values?

Front

Equal in magnitude, but in opposite directions for each substance.

Back

What is \(\Delta E_{rxn}\)?

Front

$$\Delta E_{rxn} = q_v + w$$

Back

If a chemical equation can be expressed as the sum of a series of steps, what is \(\Delta H_{rxn}\) for the overall equation?

Front

The sum of the heats of reaction for each step

Back

What is \(q_v\)?

Front

Heat at constant volume

Back

The equation relating heat, temperature change, mass, and specific heat.

Front

$$Q = m C \Delta T$$

Back

Heat capacity of a calorimeter

Front

$$\frac{\text{Total amount of heat}}{\text{Temperature change}}$$

Back

Units of specific heat

Front

$$\frac{\text{energy}}{\text{mass} \cdot \text{temperature}}$$

 

Typically,

 

$$\frac{J}{g \cdot C \degree}$$

Back

How do we calculate \(q_{soln}\)?

Front

$$q_{soln} = m_{soln} \cdot C_{s, soln} \cdot \Delta T$$

Back

The standard enthalpy of formation is also called __

Front

Standard heat of formation

Back

What is \(q_p\)?

Front

Heat at constant pressure

Back

Relate \(q_{rxn}\) and \(q_{soln}\)

Front

$$q_{rxn} = −q_{soln}$$

Back