Interpretation:
Whether molecules of period 2 are paramagnetic like oxygen molecule or not have to be determined.
Concept Introduction:
Molecular orbital diagram is a linear combination of atomic orbitals of similar energy and similar symmetry. It is formed by the proper overlap of the atomic orbitals.
There are 3 types of molecular orbitals as follows:
1. Bonding molecular orbital: They are formed by the constructive interference of atomic orbitals and electrons in it stabilize the molecule and are of lesser in energy.
2. Antibonding molecular orbital: This type of orbitals increases the energy of molecule and destabilizes it and weakens the bond between the atoms.
3. Non-bonding molecular orbital: These types of orbitals have energy similar to atomic orbitals that is addition or removal of electron does not change the energy of molecule.
The order of energy in molecular orbital follows two rules as follows:
1. For
2. For atomic number more than 14 order of energy is,
Bond order

Want to see the full answer?
Check out a sample textbook solution
Chapter 2 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate 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_forward
- Question 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_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol.arrow_forward
- 2,2-Dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol. Indicate the products obtained.arrow_forwardAdd conditions above and below the arrow that turn the reactant below into the product below in a single transformationADS fint anditions 百 Abl res condinese NC ง Add on condtions 1.0 B H,N.arrow_forward3. Provide all the steps and reagents for this synthesis. OHarrow_forward
- Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistryChemistryISBN: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: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning





