
General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 5, Problem 5.54SP
Interpretation Introduction
Interpretation:
From the given molecular orbital diagram, which of the three is likely to be stable, the bond order of the each and which contain unpaired electrons has to be determined.
Concept introduction:
Bond order:
- Bond order is nothing but the number of
chemical bonds that involved in between a pair of atoms. - Bond order indicates the stability of a bond and it reflects the stability of the molecule.
- An element having bond order zero value is not exit in the universe, but compounds may have a bond order of zero.
- According to molecular orbital theory bond order can be calculated by using the following formula.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
For the titration of a divalent metal ion (M2+) with EDTA, the stoichiometry of the reaction is typically:
1:1 (one mole of EDTA per mole of metal ion)
2:1 (two moles of EDTA per mole of metal ion)
1:2 (one mole of EDTA per two moles of metal ion)
None of the above
Please help me solve this reaction.
Indicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.
Chapter 5 Solutions
General Chemistry: Atoms First
Ch. 5.1 - Predict the shapes of the following molecules or...Ch. 5.1 - Acetic acid, CH3CO2H, is the main organic...Ch. 5.1 - Benzene, C6H6, is a cyclic molecule in which all...Ch. 5.1 - What is the geometrical arrangement of charge...Ch. 5.3 - Describe the bonding in propane, C3H8, a fuel...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of each carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...
Ch. 5.4 - Identify each of the following sets of hybrid...Ch. 5.4 - The following ball-and-stick molecular model is a...Ch. 5.5 - Construct an MO diagram for the He2+ ion. Is this...Ch. 5.6 - The B2 and C2 molecules have MO diagrams similar...Ch. 5.7 - Draw two electron-dot resonance structures for the...Ch. 5.7 - Why is molecular shape so important in biological...Ch. 5.7 - Prob. 5.17CPCh. 5 - What is the geometry around the central atom in...Ch. 5 - Prob. 5.19CPCh. 5 - Prob. 5.20CPCh. 5 - Prob. 5.21CPCh. 5 - Prob. 5.22CPCh. 5 - Prob. 5.23CPCh. 5 - Prob. 5.24SPCh. 5 - Prob. 5.25SPCh. 5 - Prob. 5.26SPCh. 5 - How many charge clouds are there around central...Ch. 5 - Prob. 5.28SPCh. 5 - Prob. 5.29SPCh. 5 - What shape do you expect for each of the following...Ch. 5 - Prob. 5.31SPCh. 5 - Prob. 5.32SPCh. 5 - Prob. 5.33SPCh. 5 - What bond angles do you expect for each of the...Ch. 5 - Prob. 5.35SPCh. 5 - Prob. 5.36SPCh. 5 - Prob. 5.37SPCh. 5 - Prob. 5.38SPCh. 5 - A potential replacement for the chlorofluorocarbon...Ch. 5 - Prob. 5.40SPCh. 5 - Prob. 5.41SPCh. 5 - Prob. 5.42SPCh. 5 - Prob. 5.43SPCh. 5 - What hybridization do you expect for atoms that...Ch. 5 - Prob. 5.45SPCh. 5 - Prob. 5.46SPCh. 5 - What hybridization would you expect for the...Ch. 5 - Prob. 5.48SPCh. 5 - Prob. 5.49SPCh. 5 - Prob. 5.50SPCh. 5 - Prob. 5.51SPCh. 5 - Prob. 5.52SPCh. 5 - Prob. 5.53SPCh. 5 - Prob. 5.54SPCh. 5 - Prob. 5.55SPCh. 5 - Prob. 5.56SPCh. 5 - Prob. 5.57SPCh. 5 - Prob. 5.58SPCh. 5 - Prob. 5.59SPCh. 5 - Prob. 5.60SPCh. 5 - Prob. 5.61SPCh. 5 - Prob. 5.62CHPCh. 5 - The following molecular model is a representation...Ch. 5 - Prob. 5.64CHPCh. 5 - Prob. 5.65CHPCh. 5 - Prob. 5.66CHPCh. 5 - Prob. 5.67CHPCh. 5 - Calcium carbide, CaC2, reacts with water to...Ch. 5 - Prob. 5.69CHPCh. 5 - The N2O5 molecule has six NO bonds and two NO ...Ch. 5 - In the cyanate ion, OCN, carbon is the central...Ch. 5 - Aspirin has the following connections among atoms....Ch. 5 - Prob. 5.73CHPCh. 5 - At high temperatures, sulfur vapor is...Ch. 5 - Carbon monoxide is produced by incomplete...Ch. 5 - Prob. 5.76CHPCh. 5 - Prob. 5.77CHPCh. 5 - Prob. 5.78CHPCh. 5 - The diatomic cyanide ion (CN) and nitrosonium ion...Ch. 5 - Prob. 5.80MPCh. 5 - Prob. 5.81MPCh. 5 - Prob. 5.82MP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningGeneral Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning


Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning

Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY