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Solutions for Chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDes
Full solutions for Organic Chemistry | 6th Edition
Solutions for Chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDesGet Full Solutions
A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.
A substance composed of two or more elements united chemically in definite proportions. (Section 1.2)
The species formed when a base accepts a proton from an acid
conjugate acid–base pair
An acid and a base, such as H2O and OH-, that differ only in the presence or absence of a proton. (Section 16.2)
A compound in which two p bonds are separated from each other by exactly one s bond.
coupling (of radicals)
A radical process in which two radicals join together and form a bond.
Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects
A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.
The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)
The attractive forces between molecules.
Protons that are exchanged at a rapid rate.
The lowest unoccupied molecular orbital.
A theory that accounts for the allowed states for electrons in molecules.(Section 9.7)
A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.
A voltaic cell that cannot be recharged. (Section 20.7)
A process of reasoning backwards from a target molecule to a suitable set of starting materials.
The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).
Atomic orbitals that are achieved by mathematically averaging one s orbital with only one p orbital to form two hybridized atomic orbitals.
A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.
A geometry adopted by an atom that has one lone pair and a steric number of 4.