ATKINS' PHYSICAL CHEMISTRY
11th Edition
ISBN: 9780190053956
Author: ATKINS
Publisher: Oxford University Press
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 14, Problem 14C.1BE
Interpretation Introduction
Interpretation:
The vapour pressure of bulk water at
Concept introduction:
Liquids are formed due to particles being apart from 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
None
None
n Feb 3
A
T
+
4. (2 pts) Draw the structure of the major component of the Limonene isolated. Explain how
you confirmed the structure.
5. (2 pts) Draw the fragment corresponding to the base peak in the Mass spectrum of
Limonene.
6. (1 pts) Predict the 1H NMR spectral data of R-Limonene.
Proton NMR: 5.3 pon multiplet (H Ring
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
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
- Part VI. Ca H 10 O is the molecular formula of compound Tom and gives the in the table below. Give a possible structure for compound Tom. 13C Signals summarized C1 C2 C3 C4 C5 C6 C7 13C shift (ppm) 23.5 27.0 33.0 35.8 127 162 205 DEPT-90 + DEPT-135 + +arrow_forward2. Using the following data to calculate the value of AvapH o of water at 298K. AvapH o of water at 373K is 40.7 kJ/mol; molar heat capacity of liquid water at constant pressure is 75.2J mol-1 K-1 and molar heat capacity of water vapor at constant pressure is 33.6 J mol-1 K-1.arrow_forwardPart VII. Below are the 'HNMR 13 3 C-NMR, COSY 2D- NMR, and HSQC 20-NMR (Similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H13 O. Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum ли 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 1.0 0.9 0.8 f1 (ppm)arrow_forward
- 3. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-pentene. expanded structure: Condensed structure: Skeletal formula: 4. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-methyl-3-heptene. expanded structure: Condensed structure: Skeletal formula: following structurearrow_forwardPart IV. Propose a plausible Structure w/ the following descriptions: a) A 5-carbon hydrocarbon w/ a single peak in its proton decoupled the DEPT-135 Spectrum shows a negative peak C-NMR spectrum where b) what cyclohexane dione isomer gives the largest no. Of 13C NMR signals? c) C5H120 (5-carbon alcohol) w/ most deshielded carbon absent in any of its DEPT Spectivaarrow_forward13C NMR is good for: a) determining the molecular weight of the compound b) identifying certain functional groups. c) determining the carbon skeleton, for example methyl vs ethyl vs propyl groups d) determining how many different kinds of carbon are in the moleculearrow_forward
- 6 D 2. (1 pt) Limonene can be isolated by performing steam distillation of orange peel. Could you have performed this experiment using hexane instead of water? Explain. 3. (2 pts) Using GCMS results, analyze and discuss the purity of the Limonene obtained from the steam distillation of orange peel.arrow_forwardPart III. Arrange the following carbons (in blue) in order of increasing chemical shift. HO B NH 2 A CIarrow_forward6. Choose the compound that will produce the spectrum below and assign the signals as carbonyl, aryl, or alkyl. 100 ō (ppm) 50 0 7. 200 150 Assign all of the protons on the spectrum below. 8. A B 4 E C 3 ō (ppm) 2 1 0 Choose the compound that will produce the spectrum below and assign the signals to the corresponding protons. OH 6 OH 3 2 1 0 4 ō (ppm)arrow_forward
- In the Thermo Fisher application note about wine analysis (Lesson 3), the following chromatogram was collected of nine components of wine. If peak 3 has a retention time of 3.15 minutes and a peak width of 0.070 minutes, and peak 4 has a retention time of 3.24 minutes and a peak width of 0.075 minutes, what is the resolution factor between the two peaks? [Hint: it will help to review Lesson 2 for this question.] MAU 300 200 T 34 5 100- 1 2 CO 6 7 8 9 0 2.4 2.6 2.8 3.0 3.2 3.4 3.6 3.8 4.0 4.2 4.4 4.6 4.8 5.0 5.2 Minutes 3.22 0.62 1.04 O 1.24arrow_forwardThe diagram shows two metals, A and B, which melt at 1000°C and 1400°C. State the weight percentage of the primary constituent (grains of C) that would be obtained by solidifying a 20% alloy of B. 1000°C a+L L+C 900°С 12 α a+C 45 1200 C L+y 140096 C+Y a+ß 800°C 700°C C+B 96 92 a+B 0 10 20 30 40 50 60 70 80 90 100 A % peso B Barrow_forward8. Choose the compound that will produce the spectrum below and assign the signals to the corresponding protons. 2 4 3 ō (ppm) OH 4 6 6 СОН 2 1 0arrow_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 Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary 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