![EBK GENERAL CHEMISTRY: THE ESSENTIAL CO](https://www.bartleby.com/isbn_cover_images/8220106637203/8220106637203_largeCoverImage.jpg)
Concept explainers
Interpretation:
The three resonance structures for the given molecule
Concept Introduction:
Octet rule: According to octet rule, when an atom contains eight electrons in its valence shell (outermost shell), it will be stable. Most of the atom will donate or accept electrons to its outer most orbital to satisfy the octet rule.
The Lewis structure is based on the concept of the octet rule so that the electrons shared in each atom should have 8 electrons in its outer shell.
Sometimes the
All the possible resonance structures are imaginary whereas the resonance hybrid is real.
Resonance is a method used to describe about delocalized electrons inside certain molecules or polyatomic ions since the Lewis structure can’t express it. A molecule or ion containing delocalized electrons can be represented by using several similar structures such structures are called as resonance structures or canonical structures.
The general rules to be followed for drawing resonance structures are given below:
- 1. The position of the atoms does not change only the pi electrons and a lone pair of electrons can change their positions.
- 2. The total number of valence electrons in all the resonance structures remains the same.
- 3. Octet rule must not be violated. No atom can have electrons more than 8 in its valence shell except sulphur.
- 4. Transfer of electrons between the bonds is shown by curved arrows.
Formal charge of an atom can be determined by the given formula.
![Check Mark](/static/check-mark.png)
Answer to Problem 9.54QP
The resonance structure can be drawn as,
Explanation of Solution
Total electrons in
Accordingly Lewis structure of
The resonance structures of molecule is as follows,
- Oxygen atom
Substituting these values to the equation,
- Carbon atom
Substituting these values to the equation,
- Sulphur atom
Substituting these values to the equation,
- Oxygen atom
Substituting these values to the equation,
- Carbon atom
Substituting these values to the equation,
- Sulphur atom
Substituting these values to the equation,
- Oxygen atom
Substituting these values to the equation,
- Carbon atom
Substituting these values to the equation,
- Sulphur atom
Substituting these values to the equation,
The three resonance structures for the given molecule
Want to see more full solutions like this?
Chapter 9 Solutions
EBK GENERAL CHEMISTRY: THE ESSENTIAL CO
- 5) Confidence interval. Berglund and Wichardt investigated the quantitative determination of Cr in high-alloy steels using a potentiometric titration of Cr(VI). Before the titration, samples of the steel were dissolved in acid and the chromium oxidized to Cr(VI) using peroxydisulfate. Shown here are the results (as %w/w Cr) for the analysis of a reference steel. 16.968, 16.922, 16.840, 16.883, 16.887, 16.977, 16.857, 16.728 Calculate the mean, the standard deviation, and the 95% confidence interval about the mean. What does this confidence interval mean?arrow_forwardIn the Nitrous Acid Test for Amines, what is the observable result for primary amines? Group of answer choices nitrogen gas bubbles form a soluble nitrite salt yellow oily layer of nitrosoaminearrow_forward3. a. Use the MS to propose at least two possible molecular formulas. For an unknown compound: 101. 27.0 29.0 41.0 50.0 52.0 55.0 57.0 100 57.5 58.0 58.5 62.0 63.0 64.0 65.0 74.0 40 75.0 76.0 20 20 40 60 80 100 120 140 160 180 200 220 m/z 99.5 68564810898409581251883040 115.0 116.0 77404799 17417M 117.0 12.9 118.0 33.5 119.0 36 133 0 1.2 157.0 2.1 159.0 16 169.0 219 170.0 17 171.0 21.6 172.0 17 181.0 1.3 183.0 197.0 100.0 198.0 200. 784 Relative Intensity 2 2 8 ō (ppm) 6 2arrow_forward
- Solve the structure and assign each of the following spectra (IR and C-NMR)arrow_forward1. For an unknown compound with a molecular formula of C8H100: a. What is the DU? (show your work) b. Solve the structure and assign each of the following spectra. 8 6 2 ō (ppm) 4 2 0 200 150 100 50 ō (ppm) LOD D 4000 3000 2000 1500 1000 500 HAVENUMBERI -11arrow_forward16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してしarrow_forward
- 3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CNarrow_forwardShow work..don't give Ai generated solution...arrow_forwardLabel the spectrum with spectroscopyarrow_forward
- 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
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)