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Solutions for Chapter 7.9: The Chirality Axis
Full solutions for Organic Chemistry, | 9th Edition
A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.
A CH3CO! group; also called an acetyl group
In IR spectroscopy, when two bonds are stretching out of phase with each other.
Air oxidation of materials such as unsaturated fatty acids.
In gas chromatography, a plot that identifies the retention time of each compound in the mixture.
common ion effect.
The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substances. (16.2)
The deterioration of metals by an electrochemical process. (18.7)
Cyclic polyethers whose molecular models resemble crowns.
A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)
A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)
A push or a pull. (Section 5.1)
Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)
A polymer that contains sections of one homopolymer that have been grafted onto a chain of the other homopolymer.
A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)
A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.
A Lewis base bonded to a metal atom in a coordination compound. It may bond strongly or weakly.
A member of the family of compounds having the 20-carbon skeleton of prostanoic acid
Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.
Ions that go through a reaction unchanged and that appear on both sides of the complete ionic equation. (Section 4.2)
The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers