Solutions for Chapter 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev Rule
Full solutions for Organic Chemistry, | 9th Edition
Solutions for Chapter 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev RuleGet Full Solutions
A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.
The electrode at which reduction occurs. (18.2)
An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)
The species formed when a base accepts a proton from an acid
The negative charge carried by an electron; it has a magnitude of 1.602 * 10-19 C. (Section 2.3)
Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects
Any process with a negative DH (the system gives energy to the surroundings).
Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.
Compounds that contain only carbon, fluorine, and hydrogen (no chlorine).
A nonpolar group that does not have favorable interactions with water.
A spectrum that contains radiation at only certain specific wavelengths. (Section 6.3)
The lowest unoccupied molecular orbital.
In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.
A naturally occurring mixture of gaseous hydrocarbon compounds composed of hydrogen and carbon. (Section 5.8)
partially condensed structures
A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.
The removal of an electron from an atom or molecule by absorption of light. (Section 18.2)
The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)
An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.
S (Section 3.3
From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise
The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)