Concept explainers
Interpretation: All the resonance forms of the sulfur-nitrogen anion,
Concept introduction: Formal charges play an important role in choosing between the possible molecular structures. The preferred structure is the one in which formal charges are zero.
To determine: All the resonance forms of the sulfur-nitrogen anion,

Answer to Problem 8.90QP
Solution
All the resonance forms of the sulfur-nitrogen anion,
Explanation of Solution
Explanation
The given anion is
It is given that the atoms are arranged as
Figure 1
The atoms in the resonating structures are named as a,b,c,d and e.
The formal charge on each atom of resonating structure (I) of
Formal charge is calculated by the formula,
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in nitrogen (c) is
Number of lone pair electrons in nitrogen (c) is
Number of bond pair electrons in nitrogen (c) is
To calculate the formal charge on nitrogen (c), substitute the value of valence electrons, lone pair electrons and bond pair electrons in the equation (1).
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
The formal charge on each atom of resonating structure (II) of
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in nitrogen (c) is
Number of lone pair electrons in nitrogen (c) is
Number of bond pair electrons in nitrogen (c) is
To calculate the formal charge on nitrogen (c), substitute the value of valence electrons, lone pair electrons and bond pair electrons in the equation (1).
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
The formal charge on each atom of resonating structure (III) of
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in nitrogen (c) is
Number of lone pair electrons in nitrogen (c) is
Number of bond pair electrons in nitrogen (c) is
To calculate the formal charge on nitrogen (c), substitute the value of valence electrons, lone pair electrons and bond pair electrons in the equation (1).
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
The formal charge on each atom of resonating structure (IV) of
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in nitrogen (c) is
Number of lone pair electrons in nitrogen (c) is
Number of bond pair electrons in nitrogen (c) is
To calculate the formal charge on nitrogen (c), substitute the value of valence electrons, lone pair electrons and bond pair electrons in the equation (1).
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Number of valence electrons in
Number of lone pair electrons in
Number of bond pair electrons in
To calculate the formal charge on
Conclusion
All the resonance forms of the sulfur-nitrogen anion,
Want to see more full solutions like this?
Chapter 8 Solutions
CHEMISTRY W/WRKBK AND SMARTWORK (LL)
- Can I please get help with this?arrow_forward1. Draw structures corresponding to each of the following names [3 ONLY]: A. 2,2,2-trichloroethanal (chloral). B. trans-3-isopropylcyclohexanecarbaldehyde C. What is the correct structure for 2-hydroxyacetophenone? Circle the letter of your response. a C 0 OH OH OH HO b. H3C CH 0 H d OH D. Provide IUPAC names for each structure below. 0 H C-H 0 0 CH3 H NO₂ E. The substance formed on addition of water to an aldehyde or ketone is called a hydrate or a/an: a. vicinal diol b. geminal diol C. acetal d. ketalarrow_forwardAssign this spectrumarrow_forward
- Redraw the tripeptide with or without its acidic hydrogensto demonstrate where the total charge of -2 comes from: *see imagearrow_forward2. Consider the data below to answer the following questions. Cyanohydrins are important intermediates in the synthesis of α-hydroxycarboxylic acids from ketones and aldehydes. The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid. Nitriles can also be hydrolyzed to carboxylic acids using aqueous base. Unfortunately, when a cyanohydrin is treated with aqueous base the original carbonyl compound is isolated. OH CH-COOH 0 HO CN C H30* C. H H HC N NaOH H₂O C=O 0 cyanohydrin H + NaCN + H₂Oarrow_forwardAssign all integrated peaksarrow_forward
- - Consider the data in the Table below to answer the following questions: Acidities of Substituted Benzoic and Acetic Acids pk,s at 25C Y-CH COOH Y Y - CH₂COOH meta para H 4.75 4.19 4.19 2.47 3.64 3.55 3.57 4.09 4.46 CN OCH 3 A. Draw the structure of the strongest acid in the table above. B. Explain why cyanoacetic acid and methoxyacetic acid are more acidic than their correspondingly substituted benzoic acid counterparts.arrow_forwardDraw the curved arrow mechanism for this reaction starting with 2-propanol in sulfuric acid. Show all nonzero formal charges and all nonbonded electrons in each step. Species not involved in a particular step do not need to be included in that step, and resonance forms do not need to be shown. Note that the alcohol is in much higher concentration than H₂O in this reaction. Harrow_forwardProvide reactions showing the following conversions: * see imagearrow_forward
- . Draw structures corresponding to each of the following names or Provide IUPAC names for each of the ollowing structures [for 4 ONLY]. A. 2-propylpentanoic acid. B. m-chlorobenzoic acid. D. C. O O HOC(CH2)3COH glutaricadd OH OH H3C CH3 C=C H COOH salicylicadd tiglicadd CH₂C=N Joe Marrow_forward. Provide structure(s) for the starting material(s), reagent(s) or the major organic product(s) of each of the ollowing reactions or sequences of reactions. Show all relevant stereochemistry [five only] A. O B. OET CH3 1. LIAIH, ether 2 H₂O O (CH3)2CH-C-CI + 0 0 ether (CH3)2CH-C-O-C-CH3 CH3 C. 0 OH HO CH3 ° Clarrow_forwardHow would you prepare each of the following compounds using either an acetoacetic ester synthesis or a alonic ester synthesis? Show all intermediate structures and all reagents.[Three only] A. B. COOH OH C. D. 0 H2C CHCH2CH2CCH3arrow_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





