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Solutions for Chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidation
Full solutions for Organic Chemistry | 8th Edition
Solutions for Chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidationGet Full Solutions
Compounds containing multiple aromatic rings fused together.
An !OR group where R is an alkyl group
A region of a polymer in which nearby chains are not linearly extended and are not parallel to one another.
The wave function (?) of an electron in an atom. (7.5)
The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)
A fi ve-membered cyclic form of a monosaccharide.
heat of vaporization
The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)
Hückel criteria for aromaticity
To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals
The polarization of the electron density of a covalent bond caused by the electronegativity of a nearby atom.
localized lone pair
A lone pair thatis not participating in resonance.
Anything that occupies space and has mass; the physical material of the universe. (Section 1.1)
A method for building a peptide from protected building blocks.
The concentration of a solution expressed as moles of solute per liter of solution; abbreviated M. (Section 4.5)
A conversion of one kind of nucleus to another. (Section 21.3)
Nucleophilic acyl substitution
A reaction in which a nucleophile bonded to the carbon of an acyl group is replaced by another nucleophile.
An intermediate that is believed to be formed during Wittig reactions.
A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons
Pi (p) bond
A covalent bond formed by the overlap of parallel 2p orbitals.
A crystal lattice in which the lattice points are located only at the corners of each unit cell. (Section 12.2)
A reaction that disobeys conservation of orbital symmetry.
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