CHEM10009 Study Guide - Final Guide: Thermodynamics, Internal Energy, Exothermic Process

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rubyswan228

11 Jun 2018

School

University of Melbourne

Department

Chemistry

Course

CHEM10009

Professor

Dr. David Jones

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Internal energy (U): sum of all energies of particles in system

Enthalpy (H): heat energy transferred due to temp. diff (in Joules)

Exothermic - -

Giving off energy

○

Endothermic - +

Gaining energy

○

Entropy (S): number of ways energy is distributed (J/(molK)

Increase in entropy of Universe (system + surroundings) will occur

spontaneously

Ice melting - water has higher entropy

Factors that affect entropy

Volume

Increased entropy with increased volume

○

Temp

Increased temp, increased entropy

○

Physical state

Gas > liquid > solid

○

Number of particles

More particles more entropy

○

Gibbs energy (G): energy available to do work

(-) spontaneous

(+) non-spontaneous

(0) equilibrium

For constant P and T

W = work done on the system (+ve for work done on, -ve for work done by)

W = -pV at constant pressure

○

-ve for expansion

○

+ve for compression (work is done)

○

0 for no volume change

○

Heat = q (J)

Total heat capacity = C (J/K)

System: particular part of universe

1st law of thermodynamics: energy cannot be created or destroyed

2nd law of thermodynamics: the entropy of the universe increases in the course of

a spontaneous change

The entropy of the universe never decreases

Calculating heat of reaction

Calorimeter - minimizes heat loss b/w system and surroundings

USE q = C deltaT

○

Bomb calorimeter - system remains at CONSTANT VOLUME

Hess's LAW

To calculate deltaH for another reaction from kown

Determining reaction enthalpies from enthalpies of formation

Entropy change for surroundings = heat transferred TO surroundings FROM the

system divided by temp

Q system = delta H

Gibbs free energy

Max amount of work that can be extracted from the energy of a reaction

Delta H Delta S Delta G

+ + Spontaneous only at high temps

- - Spontaneous at low temps

+ - Non-spontaneous

- + Spontaneous

Thermodynamics

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Document Summary

Internal energy (u): sum of all energies of particles in system. Enthalpy (h): heat energy transferred due to temp. diff (in joules) Entropy (s): number of ways energy is distributed (j/(molk) Increase in entropy of universe (system + surroundings) will occur spontaneously. Gibbs energy (g): energy available to do work (-) spontaneous (+) non-spontaneous (0) equilibrium. W = work done on the system (+ve for work done on, -ve for work done by) 1st law of thermodynamics: energy cannot be created or destroyed. 2nd law of thermodynamics: the entropy of the universe increases in the course of a spontaneous change. Calorimeter - minimizes heat loss b/w system and surroundings. Bomb calorimeter - system remains at constant volume. To calculate deltah for another reaction from kown. Entropy change for surroundings = heat transferred to surroundings from the system divided by temp. Max amount of work that can be extracted from the energy of a reaction.

Related Questions

For which system below would quantum effects be leastnoticeable?

-The collision of two N₂ molecules in a gas, whichchanges the rotational energy of both

-Polarization of the electron density of ethanol resulting inexcitation of vibrational motions

-An electron-sized particle moving in a 1 m³ box asthe temperature decreases by 10 degrees

-A hydrogen atom being struck by a UV photon

We have dealt with two different ensembles, canonical andmicrocanonical. Which of the following statements is inaccurateregarding these ensembles?

-The canonical ensemble is always considered as a subset of alarger reservoir, which acts as the surroundings.

-The microcanonical ensemble is defined to have constant energy,volume, and composition.

-The microcanonical ensemble is a smaller subset of microstatesof the canonical ensemble.

-The canonical ensemble is generally more useful than themicrocanonical for chemical processes.

Which statement below is most correct regarding the partitionfunction of an ensemble?

-For a given temperature, the high-energy contributions to thepartition function are more heavily weighted.

-Once a partition function is defined in a specific ensemble, itis valid in all other ensembles.

-It tells us the numerical order of the energy levels for agiven system.

-It provides a measure of the energy levels available to asystem at a given temperature.

Consider a cup-carrier from your favorite take-out restaurant.The carrier can hold four cups, and you have to place two cups (onelarge, one small) into the carrier, with no preference forposition. How many microstates can you form with two cups in thefour spaces?

-12

-8

-16

-6

Boltzmann's definition of the entropy was a breakthrough inunderstanding statistical thermodynamics. What is the bestdefinition of Boltzmann's entropy?

-The Boltzmann entropy is a count of the total distinctmicrostates in a system.

-The Boltzmann entropy is a measure of the randomness of anensemble.

-The Boltzmann entropy is a count of the accessible energylevels at a given temperature.

-The Boltzmann entropy is a measure of the useful work availablein an ensemble.

Our canonical ensemble was defined such that the temperature,volume, and number of particles were each held constant. In termsof the Legendre transform, which thermodynamic potential isfundamental in the canonical ensemble?

-The Helmholtz energy

-The internal energy

-The Gibbs energy

-The enthalpy

The equipartition principle can be used to estimate the constantvolume heat capacities of gases. Under which circumstances wouldthe full equipartition heat capacity most closelyapproximate the measured value of C_V?

-A sample of N₂ gas at 373K

-A sample of propane gas (C₃H₈) at roomtemperature

-A sample of water vapor at 373K

-A sample of Br₂ vapor at room temperature

Which factor below does not contribute to the rotationalpartition function of a molecule?

-The rotational quantum number

-The nuclear and electronic spin states

-The rotational constant(s)

-The temperature of the molecule

We were able to reduce the vibrational partition function froman infinite series to a function of a single exponential, but onlyapproximately. Which approximation below was NOT used?

-We assumed that the vibrational energy can be expressed asv?_e.

-We assumed that the energy levels were close enough to allowintegration instead of summation.

-We assumed that the vibrational motion is purely harmonic.

-We assumed that the separations are relatively small, due tohigh temperature or lower vibrational constant.

The derived partition function for an ideal gas depends on allof the physical parameters listed below except for which one?

-Molecular symmetry

-The temperature of the molecules

-The volume of the sample

-Mass of the molecules

Deriving the translational partition function is more involvedthan deriving the rotational and vibrational partition functions.Which statement below is NOT a reason for this?

-There are so many possible translational energy levels, thatthe integral does not converge to a finite value.

-The integral of translational states for a single particle mustbe taken over a 6-dimensional hypervolume.

-The degeneracy of translational states is not obvious becausethey lie so close in energy.

-Translational degrees of freedom involve interactions betweenall molecules in the sample, whereas rotations and vibrations donot.

The connection between the Equipartition Principle and thetranslational partition functions helped to demonstrate that thetemperature of a system depends on the easily excited degrees offreedom. Why should this be true?

-In systems with easily excited degrees of freedom, a change inthe entropy requires energy changes on the order of thermalenergy.

-In systems with easily excited degrees of freedom, smallincreases in the pressure make excited states more accessible,

increasing the temperature.

-In systems with easily excited degrees of freedom, thepotential energy is no longer dependent on the temperature of thesystem.

-In systems with easily excited degrees of freedom, thermalenergy is sufficient to allow one to treat the energy levels as acontinuum.

The connection between the Maxwell-Boltzmann distribution andthe translational partition function allowed us to betterunderstand the distribution of speeds. Which statement below is NOTa consequence of the translational partition function?

-The population of the lowest speeds is very small.

-The pressure of the gas increases as the velocityincreases.

-An increase in the temperature will result in shifting thedistribution to higher energies.

-The population of the highest speeds is very small.

When dealing with quantum energy levels, there are severalimportant factors to consider. Which concept below is NOT importantto quantum energy levels?

-The set of quantum numbers

-Degeneracy

-The deBroglie wavelength

-The ground state

HERE IS HOW THIS IS GOING TO WORK! IF YOU ANSWER THE QUESTIONS IWILL GIVE YOU THE 3K POINTS + MORE AFTER I REPOST IT.

2. The amount of heat involved in the synthesis of 1 mole of acompound from its elements, with all substances in their standardstates at 25*C, is called _________.

3. What is a valid unit for specific heat?

4. Use Hess's Law to find the heat of reaction in the examplebelow.

N2O4 (g) ----> 2NO2 (g)

Given that:

N2O4 (g) ----> N2 (g) + 2O2 (g) (Delta H =-9.7kJ)

2NO2 (g) ----> 2O2(g) + N2(g) ( Delta H= -67.7kJ)

5. Use Hess's Law to find the heat of reaction in the examplebelow. (Example doesn't exist btw.)

6. (Delta H) for the formation of rust (Fe2O3) is -826 kJ/mol. Howmuch energy is involved in the formation of 5 grams ofrust?

7. How many kilocalories of heat are required to raise thetemperature of 50g of aluminum from -5*C to 35*C? (Specific heat ofAluminum = 0.21 cal/g*C)

8.Calculate the (Delta H) for this reaction:

Zn(s) + Cu (2+ ion)(aq) ---> Zn(2+) + Cu(s)

(Delta H) for Cu(2+) = +64.4 kJ/Mol; (Delta H) for Zn(2+) = -152.4kJ/mol

9. The following equation shows the reaction that occurs whennitroglycerine explodes.

4C3H5O9N3 ----> 12CO2 + 6N2 + O2 +10H2O + 1725 Kcal

Is this reaction exothermic , endothermic, a combustion reaction ,or a combination reaction?

10. What does it mean for ammonia, (NH3) to have a (Delta H f) =-46 kJ/mol?

(for example: Define heat of formation. What does a negative heatof formation mean? what do the units of kJ/mol mean?)

11. What is the maximum amount of KCl that can dissolve in 500g ofwater?

(solubility of KCl is 34 g/ 100g of water at 20*C)

12.List the ways(operations) that can help make a substancedissolve faster in a solvent?

13. If a crystal added to an aqueous solution causes many particlesto come out of solution, the original solution was (saturate,unsaturated, supersaturated).

14. What is the number of moles of solute in 165 mL of a 0.82 Msolution?

15. What mass of NaCl is needed to make 350 mL of a 1.00 Msolution?

16. Colligative properties depend upon...

17. If one mole of each of these solutes in added to the sameamount of water, which solution has the highest boiling point?(glucose, aluminum sulfate, magnesium acetate, copper (I)chloride)

18. When an acid reacts with a base, what compounds areformed?

19. If the [H+] in a solution is 1x10^(-13) mol/L, what is the[OH-]?

20. If the [OH-] = 1x10^-6 mol/L, what is the pH of thesolution?

21. For a solution to be considered acidic what must be thehydrogen-ion concentration?

22. Which of the following represents a Bronsted-Lowry conjugateacid-base pair?

a) SO3(2-) and SO2 b) CO3(2-) and CO c) H3O and H2 d) NH4(+) and NH3

23. With solutions of "strong" acids and "strong" bases, the word"strong" refers to ...

24. What are the products of Al(OH)3 + H2CO3?

25.What is the concentration of hydrochloric acid if 5.0 mL of acidis neutralized by 30.0 mL of 2.00M sodium hydroxide.

26. At equilibrium, what is the rate of production of reactantscompared with the rate of production of products?

27. What is the equilibrium constant for the following reaction2SO3 ---> 2SO2 + O2

28. How does an increase in pressure affect the following reaction?2SO3 (g) --> 2SO2(g) +O2(g)

29.What stresses would shift the reaction to the right?

2SO3(g) ==> 2SO2(g) + O2(g)

30. The Keq of a reaction 4.9 x 10^(-7). Are products or reactantsfavored at equilibrium?

31. In which of these systems is the entropy decreasing?

a) air escaping from a tire b) snow melting c) a gas condensing d) salt dissolving inwater

32. If an atom is reduced in a redox reaction, what must occur toanother atom in the system?

33. Identify the oxidizing agent in the following reaction: 2Na + S---> Na2S

34. What are transferred in an oxidation -reductionreaction?

35. Give the oxidation number for each atom in KMnO4.

36. Which atom has a change in oxidation number of +4 in thefollowing reaction?

K2Cr2O7 + H2O + S ----> KOH + Cr2O3 +SO2

37. What is the oxidation number of sulfur in each of the following:

a. SO3 c.SO2(2-)

b. Na2SO4 d. S2O4 (2-)

38.Fe(3+) ----> Fe represents oxidation, reduction, orhydrolysis?

39. When the half reactions Br2+ 2e- -----> 2Br- and Na---->e- + Na(+) are combined the balanced redox equation is_____________________ ( WRITE the BALANCED REDOX eq)

40. To balance the oxygen and hydrogen for a redox reaction thattakes place in basic solution, it is necessary to use whichsubstance?

41. What particle completes this nuclear equation? 55/25 Mn + 2/1 H====> _____ +2 1/0 n

42. The half-life of tungsten-182 (182/74 W) is 1.1x10^(17) years.How long would it take for a 376.2 kg sample to decay until only123.0 grams remain?

43. After 3 days, the quantity of certain radioisotope is reducedfrom 13.6 grams to 1.9 grams. Calculate the half-life of theisotope.

44. What is the name of the compound having the formulaC8H18.

45. What is the name of the following compound:

CH3---CH2----CH---CH2--C

I \

CH3 OH

46. What is an isomer? Give an isomer of hexane (C6H14) and drawit's structure.

47. What is the name of the hydrocarbons with double covalentbonds?

48. Draw the stucture for 3-methylbutanoic acid.

49. Draw the structure for methylbenzene?

50. What is the name of the following compound:

CH3----C-----CH3

CH3

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CHEM10009 Study Guide - Final Guide: Thermodynamics, Internal Energy, Exothermic Process

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