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Solutions for Chapter 16.12: Acid-Catalyzed Ring Opening of Epoxides
Full solutions for Organic Chemistry, | 9th Edition
Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)
The addition of H2 across only one face of a p bond.
The pressure exerted by Earth’s atmosphere. (5.2)
The process whereby water spontaneously forms low concentrations of H+1aq2 and OH-1aq2 ions by proton transfer from one water molecule to another. (Section 16.3)
A complex polymer resulting from the polymerization of two or more chemically different monomers. (Section 12.8)
crossed aldol reaction
An aldol reaction that occurs between different partners.
A state of balance in which opposing processes occur at the same rate. (Section 11.5)
The process by which a protein adopts its biologically active shape. (Section 24.7)
Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.
isoelectric point (pI)
For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.
The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)
The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)
A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.
A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.
A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.
The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)
A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.
An element, such as nitrogen, that forms three bonds.
The distance between consecutive peaks on a wave
Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.
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