Concept explainers
Interpretation:
The two-center orbital picture that describes each of the two weak resonance contributors of
Concept introduction:
Overlap of atomic orbitals (AOs) can be thought of as wave interference. It can be constructive or destructive. Constructive interference increases the electron density between the two nuclei (an antinode) and results in a molecular orbital (MO) of lower energy. The phases of the overlapping orbitals are the same in this case. Destructive interference reduces the electron density between the two nuclei and results in an MO of higher energy. The phases of such AOs are the opposite. Since the electron density between the two nuclei decreases, there is a node (or a nodal plane) between the two atoms.

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Chapter 14 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
- Draw the product of the reaction shown below. Ignore small byproducts that would evaporate pleasearrow_forwardPoly(ethylene adipate) is a biodegradable polyester (shown below). Identify the type of polymerization process used in the production of this polymer.arrow_forwardPolymers may be composed of thousands of monomers. draw two repeat units(dimer) of the polymer formed in this reaction. assume there are hydrogen atoms on the two ends of the dimer. ignore inorganic byproducts pleasearrow_forward
- Draw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproductsarrow_forwardDraw the product of this reaction please. Ignore inorganic byproductsarrow_forwardOne of the pi molecular orbitals of 1,3-butadiene (CH2=CHCH=CH2) is shown below. Please identify the number of nodal planes perpendicular to the bonding axisarrow_forward
- Draw the monomers required to synthesize this condensation polymer please.arrow_forwardProvide the correct systematic name for the compound shown here. Please take into account the keyboard options belowarrow_forwardcurved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s)arrow_forward
- Identify the 'cartoon' drawing of the acceptor orbital in the first mechanistic step of an electrophilic addition reaction of butadiene with HBr. Pleasearrow_forwardH- H H H H H H Identify and select all structures below that represent a constitutional isomer(s) of the compound shown above. H- H H H A. H H H H-C CI H H D. H H H H H H C C -H H C C H H H H B. H CI H H- C C H H H H E. H CI H C.arrow_forwardWhy doesn't this carry on to form a ring by deprotonating the alpha carbon and the negatively-charged carbon attacking the C=O?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
