- 16.1SE.1PE: Identifying Conjugate Acids and Bases(a) What is the conjugate base...
- 16.1SE.2PE: Identifying Conjugate Acids and Bases(a) What is the conjugate base...
Solutions for Chapter 16.1SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
Steric interactions that occur between axial substituents in a chair conformation.
A pattern of variation in the amount of light absorbed by a sample as a function of wavelength. (Section 23.5)
A reaction that achieves the addition of water across a double bond in the presence of an acid catalyst.
A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms
The wave function (?) of an electron in an atom. (7.5)
Avogadro’s number (NA)
The number of 12C atoms in exactly 12 g of 12C; it equals 6.022 * 1023 mol-1. (Section 3.4)
A reaction in which a molecule, such as HCl, HBr, HI, or HOH, is split out or eliminated from adjacent carbons
An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.
Polymers that can be broken down by enzymes produced by soil microorganisms.
C-Terminal amino acid
The amino acid at the end of a polypeptide chain having the free !COOH group.
Dalton’s law of partial pressures.
The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)
A compound in which two hydrocarbon groups are bonded to one oxygen. (Section 24.4)
A compound with the structure R2CRN!NH2.
A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.
Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)
A compound with the structure R!O!O!H.
Solids that are composed of molecules. (Sections 12.1 and 12.6)
A system for naming organic compounds.
A constant of proportionality between the reaction rate and the concentrations of reactants that appear in the rate law. (Section 14.3)
A reaction in which one substrate produces two stereoisomers in unequal amounts.