Solutions for Chapter 6.3: What Does the Structure of the Transition State Look Like?
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 6.3: What Does the Structure of the Transition State Look Like?Get Full Solutions
A measure of how closely individual measurements agree with the correct value. (Section 1.5)
A reaction in which one molecule adds to another. (24.2)
A format for naming amines containing simple alkyl groups.
A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.
An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)
A substance capable of accepting a proton. (4.3)
A compound that can speed up the rate of a reaction without itself being consumed by the reaction.
A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.
Enthalpy change, DH
The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram
A term that describes the position of equilibrium for a reaction: Keq = 3H3O+ 4 3A- 4 3HA4 3H2O4
loss of a leaving group
One of the four arrow-pushing patterns for ionic reactions.
molal boiling-point-elevation constant (Kb)
A constant characteristic of a particular solvent that gives the increase in boiling point as a function of solution molality: ?Tb = Kbm. (Section 13.5)
A process in which a substance loses one or more electrons. (Section 4.4)
The conjugate base of phenol or a substituted phenol.
A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.
A radioactive nuclide. (Section 21.1)
A law stating that the partial pressure of a solvent over a solution, Psolution, is given by the vapor pressure of the pure solvent, P° solvent, times the mole fraction of a solvent in the solution, Xsolvent: Psolution = XsolventP° solvent. (Section 13.5)
An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter
Constitutional isomers that rapidly interconvert via the migration of a proton.
a !CH"CH2 group