PHYSICAL CHEMISTRY. VOL.1+2 (LL)(11TH)
11th Edition
ISBN: 9780198826910
Author: ATKINS
Publisher: Oxford University Press
expand_more
expand_more
format_list_bulleted
Question
Chapter 13, Problem 13F.2DQ
Interpretation Introduction
Interpretation:
A physical interpretation of the relation between equilibrium constant and partition functions of the reactants and products in a reaction has to be stated.
Concept introduction:
Partition function acts as a link between
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
1) For the following molecules:
(i) Label the indicated alkenes as either cis (Z), trans (E), or N/A (for non-stereogenic
centers) by bubbling in the appropriate label on the molecule.
(ii) Complete the IUPAC name located below the structure (HINT: Put the letter of the
configuration in parentheses at the beginning of the name!)
E
z
N/A
()-3,4,6-trimethylhept-2-ene
E
Oz
O N/A
()-3-ethyl-1-fluoro-4-methylhex-3-ene
E
-+-
N/A
Me
)-2,3-dimethylpent-2-ene
(d)
(b)
E
O N/A
Br
()-5-bromo-1-chloro-3-ethyloct-4-ene
ОЕ
Z
N/A
Et
(___)-3-ethyl-4-methylhex-3-ene
E
(f) Oz
N/A
z
N/A
HO
(4.7)-4-(2-hydroxyethyl)-7-methylnona-4,7-dien-2-one
O
9:21AM Tue Mar 4
## 64%
Problem 51 of 15
Submit
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product
structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s).
Be sure to account for all bond-breaking and bond-making steps.
H
:0:
CI.
AI
:CI:
:CI:
Cl
AI
Select to Add Arrows
Select to Add Arrows
O:
Cl
:CI:
:0:
H
CI: CI
CO
Select to Add Arrows
Select to Add Arrows
:O:
CI
:0:
Cl.
10:
AI
(i) Draw in the missing lone pair(s) of electrons of the reactants on the left
(ii) Draw (curved) arrows to show the flow of electrons in the acid/base reaction on the left
(iii) Draw the products of the acid/base on the right
(iv) Select the correct label for each product as either "conjugate acid" or "conjugate base"
(a)
JOH
OH
NH₂
acid
base
(b)
De
"H
conjugate acid
conjugate acid
conjugate base
conjugate base
acid
base
conjugate acid
conjugate base
conjugate acid
conjugate base
acid
base
Chapter 13 Solutions
PHYSICAL CHEMISTRY. VOL.1+2 (LL)(11TH)
Ch. 13 - Prob. 13A.1STCh. 13 - Prob. 13B.1STCh. 13 - Prob. 13B.2STCh. 13 - Prob. 13C.1STCh. 13 - Prob. 13F.1STCh. 13 - Prob. 13F.3STCh. 13 - Prob. 13A.1DQCh. 13 - Prob. 13A.2DQCh. 13 - Prob. 13A.3DQCh. 13 - Prob. 13A.4DQ
Ch. 13 - Prob. 13A.1AECh. 13 - Prob. 13A.1BECh. 13 - Prob. 13A.2AECh. 13 - Prob. 13A.2BECh. 13 - Prob. 13A.3AECh. 13 - Prob. 13A.3BECh. 13 - Prob. 13A.4AECh. 13 - Prob. 13A.4BECh. 13 - Prob. 13A.5AECh. 13 - Prob. 13A.5BECh. 13 - Prob. 13A.6AECh. 13 - Prob. 13A.6BECh. 13 - Prob. 13A.1PCh. 13 - Prob. 13A.2PCh. 13 - Prob. 13A.4PCh. 13 - Prob. 13A.5PCh. 13 - Prob. 13A.6PCh. 13 - Prob. 13A.7PCh. 13 - Prob. 13B.1DQCh. 13 - Prob. 13B.2DQCh. 13 - Prob. 13B.3DQCh. 13 - Prob. 13B.1AECh. 13 - Prob. 13B.1BECh. 13 - Prob. 13B.2AECh. 13 - Prob. 13B.2BECh. 13 - Prob. 13B.3AECh. 13 - Prob. 13B.3BECh. 13 - Prob. 13B.4AECh. 13 - Prob. 13B.4BECh. 13 - Prob. 13B.7AECh. 13 - Prob. 13B.7BECh. 13 - Prob. 13B.8AECh. 13 - Prob. 13B.8BECh. 13 - Prob. 13B.9AECh. 13 - Prob. 13B.9BECh. 13 - Prob. 13B.10AECh. 13 - Prob. 13B.10BECh. 13 - Prob. 13B.11AECh. 13 - Prob. 13B.11BECh. 13 - Prob. 13B.12AECh. 13 - Prob. 13B.12BECh. 13 - Prob. 13B.4PCh. 13 - Prob. 13B.5PCh. 13 - Prob. 13B.6PCh. 13 - Prob. 13B.7PCh. 13 - Prob. 13B.8PCh. 13 - Prob. 13B.10PCh. 13 - Prob. 13C.1DQCh. 13 - Prob. 13C.2DQCh. 13 - Prob. 13C.1AECh. 13 - Prob. 13C.1BECh. 13 - Prob. 13C.6AECh. 13 - Prob. 13C.6BECh. 13 - Prob. 13C.7AECh. 13 - Prob. 13C.7BECh. 13 - Prob. 13C.3PCh. 13 - Prob. 13C.7PCh. 13 - Prob. 13C.8PCh. 13 - Prob. 13C.9PCh. 13 - Prob. 13D.1DQCh. 13 - Prob. 13D.2DQCh. 13 - Prob. 13D.3DQCh. 13 - Prob. 13D.4DQCh. 13 - Prob. 13D.1AECh. 13 - Prob. 13D.1BECh. 13 - Prob. 13D.1PCh. 13 - Prob. 13D.2PCh. 13 - Prob. 13E.1DQCh. 13 - Prob. 13E.2DQCh. 13 - Prob. 13E.3DQCh. 13 - Prob. 13E.4DQCh. 13 - Prob. 13E.5DQCh. 13 - Prob. 13E.6DQCh. 13 - Prob. 13E.1AECh. 13 - Prob. 13E.1BECh. 13 - Prob. 13E.2AECh. 13 - Prob. 13E.2BECh. 13 - Prob. 13E.3AECh. 13 - Prob. 13E.3BECh. 13 - Prob. 13E.4AECh. 13 - Prob. 13E.4BECh. 13 - Prob. 13E.5AECh. 13 - Prob. 13E.5BECh. 13 - Prob. 13E.6AECh. 13 - Prob. 13E.6BECh. 13 - Prob. 13E.7AECh. 13 - Prob. 13E.7BECh. 13 - Prob. 13E.8AECh. 13 - Prob. 13E.8BECh. 13 - Prob. 13E.9AECh. 13 - Prob. 13E.9BECh. 13 - Prob. 13E.1PCh. 13 - Prob. 13E.2PCh. 13 - Prob. 13E.3PCh. 13 - Prob. 13E.4PCh. 13 - Prob. 13E.7PCh. 13 - Prob. 13E.9PCh. 13 - Prob. 13E.10PCh. 13 - Prob. 13E.11PCh. 13 - Prob. 13E.14PCh. 13 - Prob. 13E.15PCh. 13 - Prob. 13E.16PCh. 13 - Prob. 13E.17PCh. 13 - Prob. 13F.1DQCh. 13 - Prob. 13F.2DQCh. 13 - Prob. 13F.3DQCh. 13 - Prob. 13F.1AECh. 13 - Prob. 13F.1BECh. 13 - Prob. 13F.2AECh. 13 - Prob. 13F.2BECh. 13 - Prob. 13F.3AECh. 13 - Prob. 13F.3BECh. 13 - Prob. 13F.3PCh. 13 - Prob. 13F.4PCh. 13 - Prob. 13F.5PCh. 13 - Prob. 13F.6PCh. 13 - Prob. 13.1IA
Knowledge Booster
Similar questions
- Could someone answer this NMR and explain please Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below.arrow_forwardMacmillan Learning Draw the acyl chloride that would give the ketone shown using the Friedel-Crafts acylation reaction. Select Draw Templates More с H о Cl 2Q Erase AICI₂arrow_forwardDraw the complete mechanism for this reaction: .OH مدید OH H2SO4 + H₂O To save you some time, the starting material has been copied into the first drawing area. However, you will still need to add any other reactants or catalysts that take part in the reaction. ན ི.. OH Add/Remove step Х ด ك Click and drag to start drawing a structure.arrow_forward
- 9:27 AM Tue Mar 4 ← Problem 64 of 15 #63% Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. 0:0 0:0 :0: N. :0: :O :0: H H. :0: Select to Add Arrows O :0: H O :0: 0:0. S. H Select to Add Arrows S :0: :0: H Harrow_forwardOrder the following organic reactions by relative rate. That is, select '1' next to the reaction that will have the fastest initial rate, select '2' next to the reaction that will have the next fastest initial rate, and so on. If two reactions will have very similar initial rates, you can select the same number next to both. If a reaction will have zero or nearly zero initial rate, don't select a number and check the box in the table instead. Note: the "Nu" in these reactions means "a generic nucleophile." ملی CI :Nu 2 он 3 H Reaction Relative Rate (Choose one) ▼ Nu :CI: zero or nearly zero Nu :Nu bi (Choose one) zero or nearly zero : Nu لی Nu :H (Choose one) zero or nearly zeroarrow_forward9:12 AM Tue Mar 4 66% Problem 38 of 15 Submit Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the product formed in this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Br2 FeBrз H (+) Br: H : Br----FeBr3 く a SU 00 nd earrow_forward
- Under aqueous acidic conditions, nitriles will react to form a neutral organic intermediate 1 that has an N atom in it first, and then they will continue to react to form the final product 2: ☐ : P Draw the missing intermediate 1 and the final product 2 in the box below. You can draw the two structures in any arrangement you like. CN H₂O H₂O H+ H+ Click and drag to start drawing a structure. Хarrow_forwardOrganic bases have lone pairs of electrons that are capable of accepting protons. Lone pair electrons in a neutral or negatively charged species, or pi electron pairs. Explain the latter case (pi electron pairs).arrow_forwardDescribe the propyl anion.arrow_forward
- Indicate the names of these compounds (if they exist). 0: HỌC—NH CH3CH2-CH2arrow_forwardN Classify each of the following molecules as aromatic, antiaromatic, or nonaromatic. NH O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic O nonaromatic Garrow_forwardThe conjugate base of alkanes is called alkides. Correct?.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 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