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Solutions for Chapter 20.8: Conjugation Effects in ,-Unsaturated Aldehydes and Ketones
Full solutions for Organic Chemistry, | 9th Edition
Solutions for Chapter 20.8: Conjugation Effects in ,-Unsaturated Aldehydes and KetonesGet Full Solutions
Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)
axis of symmetry
An axis about which a compound possesses rotational symmetry.
A polyhydroxyaldehyde, a polyhydroxyketone, or a substance that gives these compounds on hydrolysis.
A law stating that at constant pressure, the volume of a given quantity of gas is proportional to absolute temperature. (Section 10.3)
Compound containing only carbon, chlorine, and fluorine.
A carbohydrate containing two monosaccharide units joined by a glycosidic bond.
A higher energy state than the ground state. (Section 6.3)
Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)
A form of magnetism in which unpaired electron spins align parallel to one another. (Section 23.1)
A five-membered cyclic hemiacetal form of a carbohydrate.
Proteins that consist of chains that are coiled into compact shapes.
A polymer that isformed via anionic polymerization.
The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)
The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).
In NMR spectroscopy, a signal that is comprised of only one peak.
A sodium or potassium salt of a fatty acid
A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers as, for example, between adipic acid and hexamethylenediamine to form nylon 66. Also called condensation polymerization.
An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter
The starting alkyl halide in a substitution or elimination reaction.
A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.