
GENERAL CHEMISTRY-MOD.MASTERINGCHEM.
11th Edition
ISBN: 9780134193601
Author: Petrucci
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 13, Problem 19E
Interpretation Introduction
Interpretation:
Temperature that equilibrium established should be calculated.
Concept introduction:
During phase change temperature of the compound remain unchanged.
Clausius Clapeyron equation is represented as follows:
ln (P2P1) = -ΔvapHR (1T2 - 1T1)
Here, P is pressure, R is Universal gas constant, T is temperature and ΔvapH is change in enthalpy of vaporization.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
mical
lation
or
mula
trations,
AAAAAAAAAAAAA
Experiment #8 Electrical conductivity & Electrolytes
Conductivity of solutions
FLINN Scientific conductivity meter scale
-
RED LED
Scale
0
Green LED
OFF
OFF
1
Dim
OFF
2
medium
OFF
Bright
Dim
4
Very Bright
Medium
3
LED Conductivity
Low or None'
Low
Medium
High
very high
SE = Strong Electrolyte, FE = Fair Electrolyte
WE Weak Electrolyte, NE= Noni Electrolyte
9 0.1 M NaOH.
10. 0.1M NH3
11. D.1M HCT
12. 0.1 M HC2H3D2
13 0 m H2SO4
Prediction
observed conductivity
?
Very bright red, dim green (4)
?
Saturated
Bright red, dim green 3 Cacal)
Bright red, dim green 3
Prediction
Bright red, No green ? observed
Bright red,dim green
?
Conductivity
Just red?
I Can you help me understand how I'm supposed
to find the predictions of the following solutions?
I know this is an Ionic compound and that
the more ions in a solution means it is able
to carry a charge, right?
AAAAAA
The light are not matching up with the scale
So I'm confused about what I should be…
Label these peaks in H- NMR and C- NMR
Complete the following table. The only density needed is already given. Show your
calculations in a neat and easy-to-follow manner in the space below the table. All units
should be included and significant figures should be given close attention. Be sure to notice
that the amount of material should be in millimoles rather than moles, and the theoretical
mass of the product should in milligrams rather than grams.
LOCH 3
+
H2SO4
HNO 3
O=C-OCH 3
NO2
x
H₂O
F.W.
4.0 mL 1.3 M
amount
0.50 mL
in H2SO4
mg Theoretical
Theoretical
mmoles
density
1.09
Chapter 13 Solutions
GENERAL CHEMISTRY-MOD.MASTERINGCHEM.
Ch. 13 - Prob. 1ECh. 13 - Consider a sample of ideal gas initially in a...Ch. 13 - Prob. 3ECh. 13 - Prob. 4ECh. 13 - Indicate whether each of the following changes...Ch. 13 - Arrange the entropy changes of the following...Ch. 13 - Prob. 7ECh. 13 - Prob. 8ECh. 13 - Indicate whether entropy increases or decreases in...Ch. 13 - Which substance in each of the following pairs...
Ch. 13 - Without performing any calculations or using data...Ch. 13 - By analogy to tH and tG how would you would you...Ch. 13 - Calculate the entropy change, S , for the...Ch. 13 - Calculate the entropy change, S , for the...Ch. 13 - IN Example 13-3, we dealt with vipH and vipH for...Ch. 13 - Pentane is one of the most volatile of the...Ch. 13 - Prob. 17ECh. 13 - Estimate the normal boiling point of bromine. Br2,...Ch. 13 - Prob. 19ECh. 13 - Refer to Figure 12-28 and equation (13.13) Which...Ch. 13 - Which of the following changes m a thermodynamic...Ch. 13 - If a reaction can be carried out only because of...Ch. 13 - Indicate which of the four cases in Table 13.3...Ch. 13 - Indicate which of the four cases in Table 13....Ch. 13 - For the mixing of ideal gases (see Figure 13-3),...Ch. 13 - In Chapter 14,, we will see that, for the...Ch. 13 - Explain why (a) some exothermic reactions do not...Ch. 13 - Explain why you would expect a reaction of the...Ch. 13 - From the data given in the following table,...Ch. 13 - Use data from Appendix D to determine values of tG...Ch. 13 - At 298 K, for the reaction...Ch. 13 - At 298 K, for the reaction...Ch. 13 - The following tG values are given for 25C ....Ch. 13 - The following tG values are given for 25C ....Ch. 13 - Write an equation for the combustion of one mole...Ch. 13 - Use molar entropies from Appendix D, together with...Ch. 13 - Assess the feasibility of the reaction...Ch. 13 - Prob. 38ECh. 13 - For each of the following reactions, write down...Ch. 13 - H2(g) can be prepared by passing steam over hot...Ch. 13 - In the synthesis of gasesous methanol from carbon...Ch. 13 - Prob. 42ECh. 13 - Use data from Appendix D to determine K at 298 K...Ch. 13 - Use data from Appendix D to establish for the...Ch. 13 - Use data from Appendix D to determine value at 298...Ch. 13 - Prob. 46ECh. 13 - Use thermodynamic data at 298 K to decide in with...Ch. 13 - Use thermodynamic data at 298 K to decide m which...Ch. 13 - For the reaction below, tG=27.07kJmol1 at 298 K....Ch. 13 - For the reaction below, tG=29.05kJmol1 at 298 K....Ch. 13 - For the reaction 2NO(g)+O2(g)2NO2(g) all but one...Ch. 13 - Prob. 52ECh. 13 - Prob. 53ECh. 13 - For the reaction 2SO2(g)+O2(g)2SO2(g),Kz=2.8102M1...Ch. 13 - Prob. 55ECh. 13 - Prob. 56ECh. 13 - Prob. 57ECh. 13 - Prob. 58ECh. 13 - To establish the law of conservation of mass,...Ch. 13 - Currently, CO2 is being studied as a source of...Ch. 13 - Prob. 61ECh. 13 - A possible reaction for converting methanol to...Ch. 13 - What must be the temperature W the following...Ch. 13 - Prob. 64ECh. 13 - The synthesis of ammonia by the Haber process...Ch. 13 - Use data from Appendix D to determine (a) tH,tS ,...Ch. 13 - Prob. 67ECh. 13 - The blowing equilibrium constants have been...Ch. 13 - For the reaction N 2 O 4 ( g ) 2N O 2 ( g ) , H e...Ch. 13 - Prob. 70ECh. 13 - Prob. 71ECh. 13 - Prob. 72ECh. 13 - Titanium is obtained by the reduction of TiCl4(l)...Ch. 13 - Prob. 74ECh. 13 - Prob. 75ECh. 13 - Prob. 76ECh. 13 - Prob. 77IAECh. 13 - Prob. 78IAECh. 13 - Consider the following hypothetical process in...Ch. 13 - One mole of argon gas, Ar(g), undergoes a change...Ch. 13 - Prob. 81IAECh. 13 - Consider the vaporization of water: H2O(l)H2O(g)...Ch. 13 - Prob. 83IAECh. 13 - Prob. 84IAECh. 13 - The following table shows the enthalpies end Gibbs...Ch. 13 - Prob. 86IAECh. 13 - Prob. 87IAECh. 13 - Prob. 88IAECh. 13 - Prob. 89IAECh. 13 - Prob. 90IAECh. 13 - Prob. 91IAECh. 13 - Prob. 92IAECh. 13 - Prob. 93IAECh. 13 - Prob. 94IAECh. 13 - Prob. 95IAECh. 13 - Use the following data to estimate,...Ch. 13 - Prob. 97IAECh. 13 - Prob. 98IAECh. 13 - Prob. 99IAECh. 13 - Prob. 100FPCh. 13 - The graph shows how shows how tG varies with...Ch. 13 - Prob. 102FPCh. 13 - Prob. 103FPCh. 13 - Prob. 104FPCh. 13 - Prob. 105SAECh. 13 - Briefly describe each of the following ideas,...Ch. 13 - Prob. 107SAECh. 13 - Prob. 108SAECh. 13 - Prob. 109SAECh. 13 - The reaction, 2Cl2O(g)2Cl2(g)+O2(g)tH=161kJ , is...Ch. 13 - Prob. 111SAECh. 13 - Prob. 112SAECh. 13 - Prob. 113SAECh. 13 - Prob. 114SAECh. 13 - Prob. 115SAECh. 13 - Prob. 116SAECh. 13 - Which of the following graphs of Gibbs energy...Ch. 13 - At room temperature and normal atmospheric...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Kumada Coupling: 1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a mechanism and give two reasons why you would NOT get the desired product. Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene. Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardWintergreen from Aspirin: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? 2. Write the mechanism of the esterification reaction you did. 3. What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of ZybanⓇ: 1. Write a mechanism for the bromination of m-chloropropiophenone. Br₂ CH2Cl2 Cl Br 2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks). 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Synthesis of Ibuprofen-Part 2: 1. Some pain relievers including ibuprofen (MotrinⓇ) and naproxen (Aleve®) are "α-arylpropanoic acids." Look up the structure of naproxen (AleveⓇ), another a-arylpropionic acid. Using the same reactions that we used for making ibuprofen, show how to make naproxen from the compound below. Show all intermediates and reagents in your synthesis. Show how you would prepare ibuprofen starting from p-isobutylbenzene rather than p-isobutylacetophenenone. What reaction steps would need to change/add? 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAcid Catalyzed Aromatization of Carvone: 1. Starting with the ketone, below, draw a mechanism for the reaction to give the phenol as shown. H2SO4 HO- H₂O 2. Why do we use CDCl instead of CHCl, for acquiring our NMR spectra? 3. Why does it not matter which enantiomer of carvone is used for this reaction? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAssign this H NMRarrow_forward
- Please complete these blanks need that asaparrow_forwardNitration of Methyl Benzoate: 1. Predict the major product for the reaction below AND provide a mechanism. Include ALL resonance structures for the intermediate. C(CH3)3 NO₂* ? 2. Assuming the stoichiometry is 1:1 for the reaction above, what volume of concentrated nitric acid would be required to mononitrate 0.50 grams of the compound above? What product(s) might you expect if you nitrated phenol instead of methyl benzoate? Explain your reasoning. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSodium Borohydride Reduction (continued on the next page): 1. Draw the product of each of the reactions below and give the formula mass to the nearest whole number. ? (1) NaBH (2) acid (1) NaBD4 (2) acid ? 2. In mass spectra, alcohols typically break as shown in equation 8 in chapter 11 (refer to your lab manual). The larger group is generally lost and this gives rise to the base peak in the mass spectrum. For the products of each of the reactions in question # 1, draw the ion corresponding to the base peak for that product and give its mass to charge ratio (m/z). 3. Given the reaction below, calculate how many mg of 1-phenyl-1-butanol that can be produced using 31 mg NaBH4 and an excess of butyrophenone. 4. + NaBH4 OH (after workup with dilute HCI) What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Aspirin from Wintergreen: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? Write a step-by-step mechanism for the esterification of salicylic acid with acetic anhydride catalyzed by concentrated H₂SO4. 3. Calculate the exact monoisotopic mass of aspirin showing your work. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 1: 1. What characteristic absorption band changes would you expect in the IR spectrum on going from p-isobutylacetophenone to 1-(4-isobutylphenyl)-ethanol and then to 1-(4-isobutylphenyl)-1-choroethane as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. Given that the mechanism of the chlorination reaction today involves formation of a benzylic carbocation, explain why the following rearranged product is not formed. محرم محمد 3. Why do we use dilute HCl for the first step of the reaction today and concentrated HCI for the second step? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAssign only the C NMRarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning

Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning

Chemical Equilibria and Reaction Quotients; Author: Professor Dave Explains;https://www.youtube.com/watch?v=1GiZzCzmO5Q;License: Standard YouTube License, CC-BY