- 20.10SE.1PE: Using Standard Reduction Potentials to Calculate ?G° and K(a) Use t...
- 20.10SE.2PE: Using Standard Reduction Potentials to Calculate ?G° and K(a) Use t...
Solutions for Chapter 20.10SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
The product obtained from 1,4-addition across a conjugated p system.
activated complex (transition state)
The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)
A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)
basic oxide (basic anhydride)
An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)
Center of symmetry
A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.
A type of double-stranded DNA in which the 59 and 39 ends of each strand are joined by phosphodiester groups.
A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.
A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.
A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)
Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)
Enantiomeric excess (ee)
The difference between the percentage of two enantiomers in a mixture
Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects
A compound containing a hydroxyl group bonded to a doubly bonded carbon atom.
A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules
When considering electrons in atomic orbitals, a rule that states that one electron is placed in each degenerate orbital first, before electrons are paired up.
A compound containing an !OOH group.
A way to view a molecule by looking along a carbon-carbon single bond
A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).
A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A counterclockwise sequence for 1-2-3 is designated as S.
A polymer in which the repeating units contain chirality centers which have alternating configuration.