
To find:
a) Draw Lewis structure for possible arrangement of
b) Assign formal charges of each structure.
c) Give reason why structure is not stable.

Answer to Problem 4.113QA
Solution:
a) i) ii)
b) i) Formal charge on each N is -1 and on O is +2.
ii) Formal charge on one of N is -2 and on O is +2.
c) In both structure the formal charge on oxygen is +2. Since oxygen is more electronegative than Nitrogen none of these structure is stable.
Explanation of Solution
1) Concept:
Each molecule contains two Nitrogen and one oxygen has an overall charge zero. Nitrogen and oxygen are in group 15 and 16 and have bonding capacity three and two. Nitrogen can show hypervalency.
2) Calculations:
The number of valence electrons are,
Elements | Valence electrons | ||
Symbol | Number of atom | In one atom | Total |
N | 2 | 5 | 10 |
O | 1 | 6 | 6 |
Valence electrons in molecule | 16 |
First possible arrangement of
Second possible arrangement of
Formula:
To find formal charge we need to use following equation,
Calculation:
Step 1) Calculations of formal charge on atoms in first structure,
Step 2) Calculations of formal charge on atoms in second structure,
Oxygen has electronegativity 3.5 and nitrogen has electronegativity 3.0. Thus, structures with formal negative charges on nitrogen and formal positive charges on oxygen are not preferred. Therefore none of these structures is stable.
Conclusion:
a) Lewis structure for possible arrangement of
i) ii)
b) i) Formal charge on each N is -1 and on O is +2.
ii) Formal charge on one of N is -2 and on O is 2+
c) Oxygen is more electronegative than Nitrogen and each of structure contains +2 charge on oxygen so none of these structure is likely to be stable.
Want to see more full solutions like this?
Chapter 4 Solutions
Chemistry: An Atoms-Focused Approach (Second Edition)
- What are is the organic molecule X and product Y of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardAt 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Without using graphs, calculate the order of the reaction. t/s [R]/(mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardPredict the organic products that form in the reaction below, and draw the skeletal ("line") structures of the missing organic products. Please include all steps & drawings & explanations.arrow_forward
- What are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forwardWhat are the products of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardWhat would happen if you added the HCI to the Grignard reagent before adding benzophenone? Draw a reaction mechanism to support your answer.arrow_forward
- At 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Calculate the order of the reaction. t/s [R]/ (mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardWrite the correct IUPAC names of the molecules in the picturearrow_forwardHow many grams of solid NaCN have to be added to 1.5L of water to dissolve 0.18 mol of Fe(OH)3 in the form Fe(CN)63 - ? ( For simplicity, ignore the reaction of CN - ion with water) Ksp for Fe(OH)3 is 2.8E -39, and Kform for Fe(CN)63 - is 1.0E31arrow_forward
- Draw the most stable chair conformation of 1-ethyl-1-methylcyclohexane, clearly showing the axial and equatorial substituents. [4] Draw structures corresponding to the following IUPAC name for each of the following compounds; [5] i) 4-Isopropyl-2,4,5-trimethylheptane ii) trans-1-tert-butyl-4-ethylcyclohexane iii) Cyclobutylcycloheptane iv) cis-1,4-di-isopropylcyclohexane (chair conformation) v) 3-Ethyl-5-isobutylnonanearrow_forwardDraw and name molecules that meet the following descriptions; [4] a) An organic molecule containing 2 sp2 hybridised carbon and 1 sp-hybridised carbon atom. b) A cycloalkene, C7H12, with a tetrasubstituted double bond. Also answer question 2 from the imagearrow_forwardH 14. Draw the line angle form of the following molecule make sure you use the proper notation to indicate spatial positioning of atoms. F F H 15. Convert the following condensed form to line angle form: (CH3)3CCH2COCH2CON(CH2CH3)2arrow_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





