- 24.4SE.1PE: Naming unsaturated HydrocarbonsName the following compounds: If a c...
- 24.4SE.2PE: Naming unsaturated HydrocarbonsName the following compounds: Draw t...
Solutions for Chapter 24.4SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A carboxylic acid that contains an amino 1¬NH22 group attached to the carbon atom adjacent to the carboxylic acid 1¬COOH2 functional group. (Section 24.7)
The hemiacetal or acetal carbon of the cyclic form of a carbohydrate
A rule that determines the order in which orbitals are filled by electrons. Specifically, the lowest energy orbital is filled first.
A reaction in which a molecule, such as HCl, HBr, HI, or HOH, is split out or eliminated from adjacent carbons
An sp3 -hybridized carbon bonded to a benzene ring
Bonding molecular orbital
A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals
The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)
Haloalkane (alkyl halide)
A compound containing a halogen atom covalently bonded to an sp3 -hybridized carbon atom. Given the symbol R!X.
An ion formed by the addition of an electron to a hydrogen atom: H-. (Section 7.7)
nucleophilic aromatic substitution
A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.
A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond
The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).
A compound that does not rotate plane-polarized light.
partially condensed structures
A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.
A substance capable of dissociating more than one proton in water; H2SO4 is an example. (Section 16.6)
reaction quotient (Q)
The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)
A method that chemists use to deal with the inadequacy of bond-line drawings.
A pericyclic reaction in which one s bond is formed at the expense of another.
An addition reaction in which two groups are added to the same face of a p bond.
An ester of glycerol with three fatty acids
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