Interpretation:
The ionic bond formed between Barium and Nitrogen needs to be explained using electronic configuration diagram
Concept introduction:
Molecules are bound together by different types of bonds namely ionic and covalent. Ionic bonds are formed when there is complete transfer of electrons from one atom to another. These atoms either lose or gain electrons to become negatively or positively charged ions. The forces of attraction between these ions cause the ionic bond formation.
Electronic configuration of atoms depicts the distribution of electrons in its energy shells following certain set of rules laid down by Aufbau’s Principle.

Answer to Problem 71A
The ionic compound Barium
Explanation of Solution
Ionic bonds involve the transfer of electrons from one atom to the other. The metal atoms, an electrons donor, loses electrons to form a positively charged ion while the non-metal atoms, electron acceptor, gains electrons to form negatively charged ions. During the process of donating or gaining electrons, the atoms follow octet rule to attain a stable noble gas configuration.
Barium has
Nitrogen has atomic number of 7 with electronic configuration as
To form compound between Barium and Nitrogen, it can be seen that Barium ion is formed by losing two electrons to get Xenon configuration while Nitrogen ion is formed by gaining 3 electrons to get Neon configuration. To bring electrical neutrality, 3 atoms of Barium ion will combine with 2 atoms of Nitrogen ion to form a stable compound. In other words, 6 electrons donated by Barium will be taken up by 6 vacancies in Nitrogen.
The ionic compound Barium
Chapter 7 Solutions
Chemistry: Matter and Change
Additional Science Textbook Solutions
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Biology: Life on Earth (11th Edition)
Microbiology: An Introduction
Applications and Investigations in Earth Science (9th Edition)
Human Anatomy & Physiology (2nd Edition)
Campbell Biology (11th Edition)
- For each of the following reactions: Fill in the missing reactant, reagent, or product (s), indicating stereochemistry where appropriate using dashed and wedged bonds. If the reaction forms a racemic mixture, draw both structures in the box and write the word “racemic”.arrow_forward1) Draw the correct chemical structure (using line-angle drawings / "line structures") from their given IUPAC name: a. hept-3-yne b. 5-bromo-1-fluoro-4-methylpent-2-ynearrow_forward15. How many absorptions are expected in the H-NMR spectra of fee songs? Explain your were a) CH,CH,CCH,CH, O CHUCH CHCHarrow_forward
- Firefly luciferin exhibits three rings. Identify which of the rings are aromatic. Identify which lone pairs are involved in establishing aromaticity. The lone pairs are labeled A-D below.arrow_forwardWhat is the [OH⁻] of a 1.80 M solution of pyridine (C₅H₅N, Kb = 1.70 × 10⁻⁹)?arrow_forwardWhat is the percent ionization in a 0.260 M solution of formic acid (HCOOH) (Ka = 1.78 × 10⁻⁴)?arrow_forward
- Determine the pH of solution of HC3H5O2 By constructing an ICE table writing the equilibrium constant expression, and using this information to determine the pH. The Ka of HC3H5O2 is 1.3 x 10-5arrow_forwardDetermine if the following salt is neutral, acidic or basic. If acidic or basic, write the appropriate equilibrium equation for the acid or base that exists when the salt is dissolved in aqueous solution. If neutral, simply write only NR. Be sure to include the proper phases for all species within the reaction LiNO3arrow_forwardAn unknown weak acid with a concentration of 0.410 M has a pH of 5.600. What is the Ka of the weak acid?arrow_forward
- (racemic) 19.84 Using your reaction roadmaps as a guide, show how to convert 2-oxepanone and ethanol into 1-cyclopentenecarbaldehyde. You must use 2-oxepanone as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way. & + EtOH H 2-Oxepanone 1-Cyclopentenecarbaldehydearrow_forwardR₂ R₁ R₁ a R Rg Nu R₂ Rg R₁ R R₁₂ R3 R R Nu enolate forming R₁ R B-Alkylated carbonyl species or amines Cyclic B-Ketoester R₁₁ HOB R R₁B R R₁₂ B-Hydroxy carbonyl R diester R2 R3 R₁ RB OR R₂ 0 aB-Unsaturated carbonyl NaOR Aldol HOR reaction 1) LDA 2) R-X 3) H₂O/H₂O ketone, aldehyde 1) 2°-amine 2) acid chloride 3) H₂O'/H₂O 0 O R₁ R₁ R R₁ R₁₂ Alkylated a-carbon R₁ H.C R₁ H.C Alkylated methyl ketone acetoacetic ester B-Ketoester ester R₁ HO R₂ R B-Dicarbonyl HO Alkylated carboxylic acid malonic ester Write the reagents required to bring about each reaction next to the arrows shown. Next, record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as forma- tion of an important intermediate, as a helpful reminder. You may want to keep track of all reactions that make carbon-carbon bonds, because these help you build large molecules from smaller fragments. This especially applies to the reactions in…arrow_forwardProvide the reasonable steps to achieve the following synthesis.arrow_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





