Thermochemistry Chapter 9 Lecture 3 Flashcards

1
Q

Thermodynamic state of a system

A

Specifying values of a set of measurable properties sufficient to determine all other properties.
e.g. n, P, and T determine states of an ideal gas. V=nRT/P d=m/v = nM/v = PM/RT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

State function

A

unique value for a specified state of a system.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

State function: Extensive examples

A

Volume, Mass, Internal Energy, Enthalpy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

State function Intensive

A

Density, Pressure, Temperature

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Path dependent Extensive

A

Heat, Work

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Path dependent Intensive

A

Heat, Capacity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

First Law of Thermodynamics

A

(Uf-Ui) = q + w = q -P (Vf-Vi)
Change in the internal energy of the closed system (U) is equal to the amount of work + heat supplied to the system.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Enthalpy H

A

Extensive state function that is the sum of the internal energy and pressure-volume product: H = U + PV or (Hf-Hi) = (Uf-Ui) + P(Vf-Vi)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What happens when there is constant pressure for Enthalpy?

A

Only heat can be gained or loss by function H=qp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Standard Enthalpy of reaction

A

(Hrxn) Change that occurs when all the reactants and products are in standard states.
Examples:
Gas: pure gas at 1 atm
liquid: pure liquid at 1 atm
Solid: pure solid at 1 atm
Solute: At concentration of 1M (mole/liter)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Hess’s law

A

Total enthalpy change = reaction is the sum of all changes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Standard Enthalpy of formation

A

(Hf) is enthalpy change in the formation of one mole of a substance in the standard state from the reference forms of its elements in standard states.
Ex: (Hf) of H2O(l) = -285.8 Kj/ mol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Allotropes

A

Different structured form of elements within the same physical state:
Ex: O2 & O3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what does it mean for (Hf-Hi)<0

A

They are stable because the enthalpy of a compound that is lower than the constitute elements and its decomposition need energy input as heat.
Usually exothermic rxns

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what does it mean for (Hf-Hi)>0

A

They are less stable because when they are greater than constitute elements, they release heat upon decomposition.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How can you calculate the change in Enthalpy?

A

Subtract the Enthalpies formation that are in the product from the enthalpy’s formation in reactant side
Product- Reactant = (Hf-Hi)

17
Q

Exothermic reactions in relation to Q

A

They are overall having a negative enthalpy reaction and q is negative because it exits the system.

18
Q

why is change in G >0 equal product in favored?

A

If G < 0 they are stable enough for reactants to turn into products the inverse happens if G <0

19
Q

what are the rules of S universe in relation to 0?

A

Suniv > 0 = product is favored
Suniv < 0 = reactant is favored
Cause less entropy overall means the reactant was probably better in having more randomness.

20
Q

If the surrounding is doing work on the system in chemical reaction

A

The moles of gas decrease

21
Q

What happens when chemical energy increases?

A

Chemical bonds break down.

22
Q

Finding Enthalpy vaporization

A

Hvap = (-R ln ( P2/P1) )/ 1/T2 - 1/T1

23
Q

Finding Pressure

A

P2 = P1 e^ Hvap/R (1/T2 - 1/T1)

24
Q

Constant of mole —> L

A

1mole =22.4L

25
Q

Finding Temp change in Hvap

A

T2= [1/T1 - Rln(P2/P1)/Hvap)^-1