Solutions for Chapter 5.18: The E1 Mechanism of Dehydrohalogenation of Alkyl Halides
Full solutions for Organic Chemistry, | 9th Edition
Solutions for Chapter 5.18: The E1 Mechanism of Dehydrohalogenation of Alkyl HalidesGet Full Solutions
The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.
An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)
One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)
A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)
A compound containing a carboxyl, !COOH, group.
E (Section 5.2C)
From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides
In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)
The practice in which water laden with sand and other materials is pumped at high pressure into rock formations to release natural gas and other petroleum materials. (Section 18.4)
A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)
Glass transition temperature (TG)
The temperature at which a polymer undergoes the transition from a hard glass to a rubbery state
Haloarene (aryl halide)
A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X
Matter that has a distinct volume but no specific shape. (Section 1.2)
A method for building a peptide from protected building blocks.
An electronwithdrawing group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the meta position.
Possessing the ability to rotate the plane of polarized light. (Section 23.4)
On an aromatic ring, the C4position.
partially condensed structures
A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.
A group that is used during synthesis to protect a functional group from the reaction conditions.
A series of structures that are melded together (conceptually) to circumvent the inadequacies of bond-line drawings.
Ions that go through a reaction unchanged and that appear on both sides of the complete ionic equation. (Section 4.2)
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