- 7.2.6: Name the following: a. CH2 CHCH2C CCH2CH3 d. HOCH2CH2C CH b. CH3CH ...
- 7.2.7: Name the following:
Solutions for Chapter 7.2: How to Name a Compound That Has More than One Functional Group
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 7.2: How to Name a Compound That Has More than One Functional GroupGet Full Solutions
Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)
An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.
A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 180°.
cholesteric liquid crystalline phase
A liquid crystal formed from flat, disc-shaped molecules that align through a stacking of the molecular discs. (Section 11.7)
The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)
Atoms that lie in the same plane.
A process during which a protein unfolds under conditions of mild heating.
Nonequivalent protons for which the replacement test produces diastereomers.
A unimolecular elimination reaction.
A bimolecular b-elimination reaction.
From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.
The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.
In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.
A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)
The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)
A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.
sigma 1S2 molecular orbital
A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)
Constitutional isomers that rapidly interconvert via the migration of a proton.
Cleavage by heating
In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.
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