Solutions for Chapter 5.16: Anti Elimination in E2 Reactions: Stereoelectronic Effects
Full solutions for Organic Chemistry, | 9th Edition
Solutions for Chapter 5.16: Anti Elimination in E2 Reactions: Stereoelectronic EffectsGet Full Solutions
Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)
A substituent lacking p bonds and comprised of only carbon and hydrogen atoms.
The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.
A compound that can serve as a proton donor.
A step in a chain reaction characterized by the reaction of a reactive intermediate and a molecule to give a new reactive intermediate and a new molecule.
A form of carbon produced when wood is heated strongly in a deficiency of air. (Section 22.9)
The isotope of hydrogen whose nucleus contains a proton and a neutron: 2 1H. (Section 22.2)
electrostatic potential maps
A three-dimensional, rainbowlike image used to visualize partial charges in a compound.
Female sex hormones.
The charge on an atom in a polyatomic ion or molecule
The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.
The lowest energy state of a system.
Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)
Numbers of protons and neutrons that result in very stable nuclei. (Section 21.2)
A collection of Avogadro’s number 16.022 * 10232 of objects; for example, a mole of H2O is 6.022 * 1023 H2O molecules. (Section 3.4)
A compound with molecular formula HONO.
The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).
A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)
The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both
In NMR spectroscopy, a signal that is comprised of only one peak.
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