- 13.8SE.1PE: Calculation of Boiling-Point Elevation and Freezing-Point Depressio...
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Solutions for Chapter 13.8SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A reaction in which one molecule adds to another. (24.2)
addition to p bond
One of the six kinds of arrow-pushing patterns used in drawing mechanisms for radical reactions. A radical adds to a p bond, destroying the p bond and generating a new radical.
A format for naming primary amines containing a complex alkyl group.
The vertical distance from the middle of a wave to the peak or trough. (7.1)
axis of symmetry
An axis about which a compound possesses rotational symmetry.
The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100
A ratio relating the same quantity in two systems of units that is used to convert the units of measurement. (Section 1.6)
A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.
directed aldol addition
A techniquefor performing a crossed aldol addition thatproduces one major product.
A compound with the structure R!S!S!R.
The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).
Haloarene (aryl halide)
A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X
The highest occupied molecular orbital.
An achiral compound possessing two or more chiral centers that also has chiral isomers
The product formed when a nucleoside is coupled to a phosphate group
A variety of enzymes that selectively hydrolyze specific peptide bonds.
A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons
A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)
A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.
Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.
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