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Solutions for Chapter 6.7SE: 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.
Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)
The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.
An electrode at which oxidation occurs. (Section 20.3)
beta (b) position
The position immediately adjacent to an alpha (a) position.
An elementary reaction that involves two molecules. (Section 14.6)
The study of matter and the changes it undergoes. (1.1)
Compounds containing the CN2 ion. (22.3)
A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)
A push or a pull. (Section 5.1)
Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.
Solids that are composed of ions. (Section 12.1)
A carbohydrate that contains a ketone group.
The NO+ ion, which is formed when NaNO2 is treated with HCl.
A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.
A method of electron book-keeping in which all bonds are treated as if they were purely ionic.
Pi (p) molecular orbital
A molecular orbital formed by overlapping parallel 2p orbitals on adjacent atoms; its electron density lies above and below the line connecting the atoms
Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.
An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.
In bond-line structures, a group in front of the page.