Table of Contents Table of Contents
Previous Page  322 / 912 Next Page
Basic version Information
Show Menu
Previous Page 322 / 912 Next Page
Page Background

314 Chapter 9

Copyright © 2017 Pearson Education, Inc.

inversion of configuration

turning the carbon inside out like an umbrella so that the resulting product has a

configuration opposite that of the reactant.

ion-dipole interaction

the interaction between an ion and the dipole of a molecule.

kinetics

the field of chemistry that deals with the rates of chemical reactions.

leaving group

the group that is displaced in a substitution reaction.

nucleophile

an electron-rich atom or molecule.

nucleophilicity

a measure of how readily an atom or a molecule with a lone pair attacks another atom.

nucleophilic substitution

a reaction in which a nucleophile substitutes for an atom or a group.

reaction

partial racemization

formation of a pair of enantiomers in unequal amounts.

protic solvent

a solvent that has a hydrogen bonded to an oxygen or to a nitrogen.

rate constant

the constant of proportionality in the rate law for a reaction; it describes how

difficult it is to overcome the energy barrier of a reaction.

rate law

the equation that shows the relationship between the rate of a reaction and the

concentration of the reactants.

regioselectivity

the preferential formation of a constitutional isomer.

sawhorse projection

a way to represent the three-dimensional spatial relationships of atoms by looking

at the carbon–carbon bond from an oblique angle.

second-order reaction

a reaction whose rate is dependent on the concentration of two reactants.

S

N

1

reaction

a unimolecular nucleophilic substitution reaction.

S

N

2

reaction

a bimolecular nucleophilic substitution reaction.

solvent-separated ion pair

an ion pair that results when the cation and anion are separated by one or more

solvent molecules.

solvolysis

reaction with a solvent.

steric effects

effects due to the fact that groups occupy a certain volume of space.

steric hindrance

caused by bulky groups at the site of a reaction that make it difficult for the reactants

to approach each other.

substitution reaction

a reaction that exchanges one substituent of a reactant for another.