Concept explainers
(a)
Interpretation:
Changes in bond order, bond distance, and magnetic properties expected when
Concept Introduction:
Bond order is calculated by the expression given as follows:
The magnetic properties are related to terms such as diamagnetism and paramagnetism. Paramagnetism defines the ability of elements to be weakly attracted in an external magnetic field. It arises due to the presence of unpaired electrons. Diamagnetism defines the ability to be repelled in the external magnetic field environment. This is because diamagnetic species have paired electrons.
The bond length is estimated to be an average of covalent radii of two atoms within a bond. When bond order increases bond becomes stronger and bond length reduces. This accounts for shorter bond length in the case of unsaturated compounds while longer bonds in saturated compounds.
(a)

Explanation of Solution
For
The corresponding molecular orbitals in
Bond order is calculated by the expression given as follows:
Substitute 4 for anti-bonding electrons and 8 for bonding electrons in equation (1).
Thus bond order is 2 in
For
Substitute 4 for anti-bonding electrons and 7 for bonding electrons in equation (1).
Thus bond order is 1.5 in
Since the reduction in bond implies bond is longer thus the bond length is more in case of
(b)
Interpretation:
Changes in bond order, bond distance, and magnetic properties expected when
Concept Introduction:
Refer to part (a).
(b)

Explanation of Solution
For
The corresponding molecular orbitals in
Bond order is calculated by the expression given as follows:
Substitute 4 for anti-bonding electron and 10 for bonding electrons in equation (1).
Thus bond order is 3 in
For
Substitute 4 for anti-bonding electrons and 9 for bonding electrons in equation (1).
Thus bond order is 2.5 in
Since the reduction in bond order implies bond is longer thus the bond length is more in case of
Further in
(b)
Interpretation:
Changes in bond order, bond distance, and magnetic properties expected when
Concept Introduction:
Refer to part (a).
(b)

Explanation of Solution
For
The corresponding molecular orbitals in
Bond order is calculated by the expression given as follows:
Substitute 6 for anti-bonding electrons and 10 for bonding electrons in equation (1).
Thus bond order is 2 in
For
Substitute 5 for anti-bonding electrons and 10 for bonding electrons in equation (1).
Thus bond order is 2.5 in
Since the reduction in bond order implies bond is shorter thus the bond length is more in case of
Further in
Want to see more full solutions like this?
Chapter 2 Solutions
CHEMICAL PRINCIPLES (LL) W/ACCESS
- Determine 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_forward
- R₂ 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_forwardIdentify which compound is more acidic. Justify your choice.arrow_forward
- Provide the reasonable steps to achieve the following synthesis.arrow_forwardWhen anisole is treated with excess bromine, the reaction gives a product which shows two singlets in 1H NMR. Draw the product.arrow_forward(ii) Draw a reasonable mechanism for the following reaction: CI NaOH heat OH (hint: SNAr Reaction) :arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning




