Solutions for Chapter 14.8: An Organozinc Reagent for Cyclopropane Synthesis
Full solutions for Organic Chemistry, | 9th Edition
Steric interactions that occur between axial substituents in a chair conformation.
For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.
The cycle that relates lattice energies of ionic compounds to ionization energies, electron affinities, heats of sublimation and formation, and bond enthalpies. (9.3)
A process by which molecular oxygen is used to convert food into CO2, water, and energy.
In NMR spectroscopy, protons (or carbon atoms) that occupy identical electronic environments and produce only one signal.
A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)
A polymer that is constructed from more than one repeating unit.
A molecule containing an !OH group and a !CN group bonded to the same carbon.
The joining of two light nuclei to form a more massive one. (Section 21.6)
A reaction in which a methyl ketone is converted into a carboxylic acid upon treatment with excess base and excess halogen, followed by aqueous acid.
Materials that do not conduct electricity. (Section 12.7)
The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)
A term that describes the position of equilibrium for a reaction: Keq = 3H3O+ 4 3A- 4 3HA4 3H2O4
Refers to groups occupying 1,3-positions on a benzene ring.
A system of measurement used in science and in most countries. The meter and the gram are examples of metric units. (Section 1.4)
A cyclic ether containing a three-membered ring system. Also called an epoxide.
A biopolymer formed from amino acids. (Section 24.7)
sigma 1S2 molecular orbital
A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)
A sodium or potassium salt of a fatty acid
A name that is assigned using the rules of IUPAC nomenclature.
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