- 6.3SE.1PE: Energy of a PhotonCalculate the energy of one photon of yellow ligh...
- 6.3SE.2PE: Energy of a PhotonCalculate the energy of one photon of yellow ligh...
Solutions for Chapter 6.3SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
Polymers that are formed via cationic addition, anionic addition, or free-radical addition.
An alloy of mercury with another metal or metals. (21.2)
An equation that relates the rate constant for a reaction to the frequency factor, A, the activation energy, Ea, and the temperature, T: k = Ae-Ea>RT. In its logarithmic form it is written ln k = -Ea>RT + ln A. (Section 14.5)
A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.
bonding atomic radius
The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)
A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.
coupling (of radicals)
A radical process in which two radicals join together and form a bond.
The term used to express the concept of less shielding in NMR
The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.
A symbol used to show that structures on either side of it are resonance-contributing structures
A protein molecule that acts to catalyze specific biochemical reactions. (Section 14.7)
A property that depends on the amount of material considered; for example, mass or volume. (Section 1.3)
The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)
The lowest unoccupied molecular orbital.
Nuclear magnetic resonance (NMR) spectroscopy
A spectroscopic technique that gives information about the number and types of atoms in a molecule, for example, hydrogens (1 H!NMR) and carbons (13C!NMR)
The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.
A nucleophilic substitution in which the solvent is also the nucleophile
Isomers that have the same molecular formula and the same connectivity of their atoms but a different orientation of their atoms in space
An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.
Groups that weakly deactivate an aromatic ring toward electrophilic aromatic substitution, thereby decreasing the rate of the reaction.
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