- 14.12SE.1PE: Determining Molecularity and Identifying IntermediatesIt has been p...
- 14.12SE.2PE: Determining Molecularity and Identifying IntermediatesIt has been p...
Solutions for Chapter 14.12SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A carbon atom adjacent to a carbonyl group
Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)
A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.
The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.
A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)
A measure of a solvent’s ability to insulate opposite charges from one another
A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis
A quantity defined by the relationship H = E + PV; the enthalpy change, ?H, for a reaction that occurs at constant pressure is the heat evolved or absorbed in the reaction: ?H = qp. (Section 5.3)
A process in which a system releases heat to its surroundings. (Section 5.2)
heat of fusion
The enthalpy change, ?H, for melting a solid. (Section 11.4)
Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.
The difference between the mass of a nucleus and the total masses of the individual nucleons that it contains. (Section 21.6)
Elements that lie along the diagonal line separating the metals from the nonmetals in the periodic table; the properties of metalloids are intermediate between those of metals and nonmetals. (Section 2.5)
In mass spectrometry,the ion that is generated when the compound is ionized.
plane of symmetry
A plane that bisects a compound into two halves that are mirror images of each other.
Primary structure of nucleic acids
The sequence of bases along the pentose-phosphodiester backbone of a DNA or RNA molecule read from the 5’ end to the 3’ end
A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.
A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.
Sanger dideoxy method
A method developed by Frederick Sanger for sequencing DNA molecules
A geometry adopted by an atom that has one lone pair and a steric number of 4.
Textbook Survival Guides
Having trouble accessing your account? Let us help you, contact support at +1(510) 944-1054 or email@example.com
Forgot password? Reset it here