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Solutions for Chapter 5.14SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
acetoacetic ester synthesis
A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.
activation energy (Ea).
The minimum amount of energy required to initiate a chemical reaction. (13.4)
A format for naming primary amines containing a complex alkyl group.
Male sex hormones.
The hemiacetal or acetal carbon of the cyclic form of a carbohydrate
An alkane containing two rings that share two carbons
A dispersion of particles of one substance (the dispersed phase) throughout a dispersing medium made of another substance. (12.8)
In an acid-base reaction, the product that results when an acid is deprotonated.
The breakdown of a compound into two or more components. (4.4)
Diamagnetic current in NMR
The circulation of electron density in a molecule in an applied magnetic fi eld.
Enantiomeric excess (ee)
The difference between the percentage of two enantiomers in a mixture
In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.
A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules
Protons that are exchanged at a rapid rate.
The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)
A substance that does not ionize in water and consequently gives a nonconducting solution. (Section 4.1)
A compound with the structure R2CRN!OH.
From the Greek, poly 1 meros, meaning many parts. Any long-chain molecule synthesized by linking together many single parts called monomers
A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.
In IR spectroscopy, when two bonds are stretching in phase with each other.
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