ATKINS' PHYSICAL CHEMISTRY-ACCESS
11th Edition
ISBN: 9780198834700
Author: ATKINS
Publisher: OXF
expand_more
expand_more
format_list_bulleted
Question
Chapter 9, Problem 9E.3BE
(i)
Interpretation Introduction
Interpretation:
The delocalization energy and the
Concept introduction:
Delocalization of energy refers to the extra stabilization of the molecule, which is due to allowing the electrons to spread over the entire molecule. To calculate the delocalization energy, the energy of the molecule in question is compared with a molecule in which electrons cannot spread over the molecule.
(ii)
Interpretation Introduction
Interpretation:
The delocalization energy and the
Concept introduction:
Delocalization of energy refers to the extra stabilization of the molecule, which is due to allowing the electrons to spread over the entire molecule. To calculate the delocalization energy, the energy of the molecule in question is compared with a molecule in which electrons cannot spread over the molecule.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
For each reaction shown below follow the curved arrows to complete each equationby showing the structure of the products. Identify the acid, the base, the conjugated acid andconjugated base. Consutl the pKa table and choose the direciton theequilibrium goes. However show the curved arrows. Please explain if possible.
A molecule shows peaks at 1379, 1327, 1249, 739 cm-1. Draw a diagram of the energy levels for such a molecule. Draw arrows for the possible transitions that could occur for the molecule.
In the diagram imagine exciting an electron, what are its various options for getting back to the ground state?
What process would promote radiation less decay?
What do you expect for the lifetime of an electron in the T1 state?
Why is phosphorescence emission weak in most substances?
What could you do to a sample to enhance the likelihood that phosphorescence would occur over radiationless decay?
Rank the indicated C—C bonds in increasing order of bond length. Explain as why to the difference.
Chapter 9 Solutions
ATKINS' PHYSICAL CHEMISTRY-ACCESS
Ch. 9 - Prob. 9B.1STCh. 9 - Prob. 9A.1DQCh. 9 - Prob. 9A.2DQCh. 9 - Prob. 9A.3DQCh. 9 - Prob. 9A.4DQCh. 9 - Prob. 9A.5DQCh. 9 - Prob. 9A.1AECh. 9 - Prob. 9A.1BECh. 9 - Prob. 9A.2AECh. 9 - Prob. 9A.2BE
Ch. 9 - Prob. 9A.3AECh. 9 - Prob. 9A.3BECh. 9 - Prob. 9A.4AECh. 9 - Prob. 9A.4BECh. 9 - Prob. 9A.5AECh. 9 - Prob. 9A.5BECh. 9 - Prob. 9A.6AECh. 9 - Prob. 9A.6BECh. 9 - Prob. 9A.7AECh. 9 - Prob. 9A.7BECh. 9 - Prob. 9A.8AECh. 9 - Prob. 9A.8BECh. 9 - Prob. 9A.1PCh. 9 - Prob. 9A.2PCh. 9 - Prob. 9A.3PCh. 9 - Prob. 9B.2DQCh. 9 - Prob. 9B.3DQCh. 9 - Prob. 9B.1AECh. 9 - Prob. 9B.1BECh. 9 - Prob. 9B.2AECh. 9 - Prob. 9B.2BECh. 9 - Prob. 9B.3AECh. 9 - Prob. 9B.3BECh. 9 - Prob. 9B.4AECh. 9 - Prob. 9B.4BECh. 9 - Prob. 9B.1PCh. 9 - Prob. 9B.2PCh. 9 - Prob. 9B.3PCh. 9 - Prob. 9C.1DQCh. 9 - Prob. 9C.2DQCh. 9 - Prob. 9C.3DQCh. 9 - Prob. 9C.4DQCh. 9 - Prob. 9C.1AECh. 9 - Prob. 9C.1BECh. 9 - Prob. 9C.2AECh. 9 - Prob. 9C.2BECh. 9 - Prob. 9C.3AECh. 9 - Prob. 9C.3BECh. 9 - Prob. 9C.4AECh. 9 - Prob. 9C.4BECh. 9 - Prob. 9C.5AECh. 9 - Prob. 9C.5BECh. 9 - Prob. 9C.6AECh. 9 - Prob. 9C.6BECh. 9 - Prob. 9C.2PCh. 9 - Prob. 9C.4PCh. 9 - Prob. 9D.1DQCh. 9 - Prob. 9D.2DQCh. 9 - Prob. 9D.3DQCh. 9 - Prob. 9D.4DQCh. 9 - Prob. 9D.1AECh. 9 - Prob. 9D.1BECh. 9 - Prob. 9D.2AECh. 9 - Prob. 9D.2BECh. 9 - Prob. 9D.3AECh. 9 - Prob. 9D.3BECh. 9 - Prob. 9D.4AECh. 9 - Prob. 9D.4BECh. 9 - Prob. 9D.5AECh. 9 - Prob. 9D.5BECh. 9 - Prob. 9D.6AECh. 9 - Prob. 9D.6BECh. 9 - Prob. 9D.7AECh. 9 - Prob. 9D.7BECh. 9 - Prob. 9D.1PCh. 9 - Prob. 9E.1DQCh. 9 - Prob. 9E.2DQCh. 9 - Prob. 9E.3DQCh. 9 - Prob. 9E.4DQCh. 9 - Prob. 9E.5DQCh. 9 - Prob. 9E.1AECh. 9 - Prob. 9E.1BECh. 9 - Prob. 9E.2AECh. 9 - Prob. 9E.2BECh. 9 - Prob. 9E.3AECh. 9 - Prob. 9E.3BECh. 9 - Prob. 9E.4AECh. 9 - Prob. 9E.4BECh. 9 - Prob. 9E.6AECh. 9 - Prob. 9E.6BECh. 9 - Prob. 9E.1PCh. 9 - Prob. 9E.2PCh. 9 - Prob. 9E.3PCh. 9 - Prob. 9E.6PCh. 9 - Prob. 9.1IACh. 9 - Prob. 9.2IACh. 9 - Prob. 9.4IA
Knowledge Booster
Similar questions
- The SN 1 mechanism starts with the rate-determining step which is the dissociation of the alkyl halide into a carbocation and a halide ion. The next step is the rapid reaction of the carbocation intermediate with the nucleophile; this step completes the nucleophilic substitution stage. The step that follows the nucleophilic substitution is a fast acid-base reaction. The nucleophile now acts as a base to remove the proton from the oxonium ion from the previous step, to give the observed product. Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all nonzero formal charges. Cl: Add/Remove step G Click and drag to start drawing a structure.arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardA monochromatic light with a wavelength of 2.5x10-7m strikes a grating containing 10,000 slits/cm. Determine the angular positions of the second-order bright line.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Us the reaction conditions provided and follow the curved arrow to draw the resulting structure(s). Include all lone pairs and charges as appropriate. H :I H 0arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_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