Atkins' Physical chemistry
11th Edition
ISBN: 9780198814740
Author: ATKINS, P. W. (peter William), 1940- (author.)
Publisher: Oxford University Press,
expand_more
expand_more
format_list_bulleted
Question
Chapter 14, Problem 14C.3AE
Interpretation Introduction
Interpretation:
The pressure differential of water across the surface of a spherical droplet of radius
Concept introduction:
Liquids are formed due to particles being apart for more than a few diameters. These molecules interact to form the liquid phase. The
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
ох
4-tert-butyl oxy cyclohex-1-ene
Incorrect, 1 attempt remaining
The systematic name of this compound classifies the -OR group as
a substituent of the hydrocarbon, which is considered the principal
functional group. The ether substituent is named with the suffix
'oxy'.
The general format for the systematic name of a hydrocarbon is:
[prefix/substituent] + [parent] + [functional group suffix]
Substituents are listed in alphabetical order. Molecules with a chiral
center will indicate the absolute configuration at the beginning of its
name with the R and S notation.
5. Compressibility (6 points total). The isothermal compressibility is a measure of how
hard/easy it is to compress an object (how squishy is it?) at constant temperature. It is
др
defined as Br=-()=-(200²)T'
(a) You might wonder why there is a negative sign in this formula. What does it mean when
this quantity is positive and what does it mean when this quantity is negative?
(b) Derive the formula for the isothermal compressibility of an ideal gas (it is very simple!)
(c) Explain under what conditions for the ideal gas the compressibility is higher or lower,
and why that makes sense.
19. (3 pts) in Chapter 7 we will see a reaction of halocyclohexanes that requires that the halogen occupy an axial position with
this in mind, would you expect cis-1-bromo-3-methylcyclohexane or trans-1-bromo-3-methylcyclohexane to be more
reactive in this reaction? Briefly explain your choice using structures to support your answer.
Mere-eries-cecleone)
The tran-i-browse-3-methylcyclohexione
Chapter 14 Solutions
Atkins' Physical chemistry
Ch. 14 - Prob. 14A.1STCh. 14 - Prob. 14A.2STCh. 14 - Prob. 14B.1STCh. 14 - Prob. 14C.1STCh. 14 - Prob. 14C.2STCh. 14 - Prob. 14D.1STCh. 14 - Prob. 14D.2STCh. 14 - Prob. 14E.1STCh. 14 - Prob. 14A.1DQCh. 14 - Prob. 14A.2DQ
Ch. 14 - Prob. 14A.3DQCh. 14 - Prob. 14A.1AECh. 14 - Prob. 14A.1BECh. 14 - Prob. 14A.2AECh. 14 - Prob. 14A.2BECh. 14 - Prob. 14A.3AECh. 14 - Prob. 14A.3BECh. 14 - Prob. 14A.4AECh. 14 - Prob. 14A.4BECh. 14 - Prob. 14A.5AECh. 14 - Prob. 14A.5BECh. 14 - Prob. 14A.6AECh. 14 - Prob. 14A.6BECh. 14 - Prob. 14A.7AECh. 14 - Prob. 14A.7BECh. 14 - Prob. 14A.8AECh. 14 - Prob. 14A.8BECh. 14 - Prob. 14A.9AECh. 14 - Prob. 14A.9BECh. 14 - Prob. 14A.1PCh. 14 - Prob. 14A.2PCh. 14 - Prob. 14A.3PCh. 14 - Prob. 14A.4PCh. 14 - Prob. 14A.5PCh. 14 - Prob. 14A.6PCh. 14 - Prob. 14A.7PCh. 14 - Prob. 14A.8PCh. 14 - Prob. 14A.10PCh. 14 - Prob. 14A.12PCh. 14 - Prob. 14A.13PCh. 14 - Prob. 14B.1DQCh. 14 - Prob. 14B.2DQCh. 14 - Prob. 14B.3DQCh. 14 - Prob. 14B.4DQCh. 14 - Prob. 14B.5DQCh. 14 - Prob. 14B.1AECh. 14 - Prob. 14B.1BECh. 14 - Prob. 14B.2AECh. 14 - Prob. 14B.2BECh. 14 - Prob. 14B.3AECh. 14 - Prob. 14B.3BECh. 14 - Prob. 14B.4AECh. 14 - Prob. 14B.4BECh. 14 - Prob. 14B.5AECh. 14 - Prob. 14B.5BECh. 14 - Prob. 14B.6AECh. 14 - Prob. 14B.6BECh. 14 - Prob. 14B.1PCh. 14 - Prob. 14B.2PCh. 14 - Prob. 14B.3PCh. 14 - Prob. 14B.4PCh. 14 - Prob. 14B.5PCh. 14 - Prob. 14B.6PCh. 14 - Prob. 14B.7PCh. 14 - Prob. 14B.8PCh. 14 - Prob. 14B.10PCh. 14 - Prob. 14C.1DQCh. 14 - Prob. 14C.2DQCh. 14 - Prob. 14C.1AECh. 14 - Prob. 14C.1BECh. 14 - Prob. 14C.2AECh. 14 - Prob. 14C.2BECh. 14 - Prob. 14C.3AECh. 14 - Prob. 14C.3BECh. 14 - Prob. 14C.4AECh. 14 - Prob. 14C.4BECh. 14 - Prob. 14C.1PCh. 14 - Prob. 14C.2PCh. 14 - Prob. 14D.1DQCh. 14 - Prob. 14D.2DQCh. 14 - Prob. 14D.3DQCh. 14 - Prob. 14D.4DQCh. 14 - Prob. 14D.5DQCh. 14 - Prob. 14D.1AECh. 14 - Prob. 14D.1BECh. 14 - Prob. 14D.2AECh. 14 - Prob. 14D.2BECh. 14 - Prob. 14D.3AECh. 14 - Prob. 14D.3BECh. 14 - Prob. 14D.4AECh. 14 - Prob. 14D.4BECh. 14 - Prob. 14D.5AECh. 14 - Prob. 14D.5BECh. 14 - Prob. 14D.6AECh. 14 - Prob. 14D.6BECh. 14 - Prob. 14D.8AECh. 14 - Prob. 14D.8BECh. 14 - Prob. 14D.9AECh. 14 - Prob. 14D.9BECh. 14 - Prob. 14D.2PCh. 14 - Prob. 14D.3PCh. 14 - Prob. 14D.4PCh. 14 - Prob. 14D.6PCh. 14 - Prob. 14D.7PCh. 14 - Prob. 14D.8PCh. 14 - Prob. 14D.9PCh. 14 - Prob. 14D.10PCh. 14 - Prob. 14E.1DQCh. 14 - Prob. 14E.2DQCh. 14 - Prob. 14E.3DQCh. 14 - Prob. 14E.4DQCh. 14 - Prob. 14E.5DQCh. 14 - Prob. 14E.1AECh. 14 - Prob. 14E.1BECh. 14 - Prob. 14E.1PCh. 14 - Prob. 14E.3PCh. 14 - Prob. 14.1IACh. 14 - Prob. 14.2IACh. 14 - Prob. 14.6IACh. 14 - Prob. 14.8IA
Knowledge Booster
Similar questions
- Please help me calculate the undiluted samples ppm concentration. My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve. Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4arrow_forwardProvide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₁₂C C(CH3)3 C=C H3C CH3 CH3CH2CH CI CH3 Submit Answer Retry Entire Group 2 more group attempts remaining Previous Nextarrow_forwardArrange the following compounds / ions in increasing nucleophilicity (least to most nucleophilic) CH3NH2 CH3C=C: CH3COO 1 2 3 5 Multiple Choice 1 point 1, 2, 3 2, 1, 3 3, 1, 2 2, 3, 1 The other answers are not correct 0000arrow_forward
- curved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the cured electron-pushing arrows for thw following reaction or mechanistic steps. be sure to account for all bond-breaking and bond making stepsarrow_forwardUsing the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.arrow_forwardSynthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4arrow_forward
- Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)arrow_forwardHi I need help on the question provided in the image.arrow_forwardDraw a reasonable mechanism for the following reaction:arrow_forward
- Draw the mechanism for the following reaction: CH3 CH3 Et-OH Et Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H± EXP. L CONT. י Α [1] осн CH3 а CH3 :Ö Et H 0 N о S 0 Br Et-ÖH | P LL Farrow_forward20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY

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

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

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

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY