- 9.7SE.1PE: Delocalized BondingDescribe the bonding in the nitrate ion. N03-. D...
- 9.7SE.2PE: Delocalized BondingDescribe the bonding in the nitrate ion. N03-. D...
Solutions for Chapter 9.7SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)
The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.
An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.
Chemical shift (d)
The shift in parts per million of an NMR signal relative to the signal of TMS
A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.
A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.
A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.
deoxyribonucleic acid (DNA)
A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)
The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.
A carbohydrate containing two monosaccharide units joined by a glycosidic bond.
A solute that produces ions in solution; an electrolytic solution conducts an electric current. (Section 4.1)
A mode of radioactive decay in which an inner-shell orbital electron is captured by the nucleus. (Section 21.1)
A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.
Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.
A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)
A phosphoric monoester, which is the simplest kind of phosphoglyceride.
The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.
A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).
A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.
An addition reaction in which two groups are added to the same face of a p bond.