Solutions for Chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONS
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONSGet Full Solutions
An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.
Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.
A galvanic cell, or a series of combined galvanic cells, that can be used as a source of direct electric current at a constant voltage. (18.6)
An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)
A term describing a molecule or an ion that cannot be superimposed on its mirror image. (Sections 23.4 and 24.5)
A type of double-stranded DNA in which the 59 and 39 ends of each strand are joined by phosphodiester groups.
A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.
Compounds containing the CN2 ion. (22.3)
A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction
An effect that causes different regions of space to be characterized by different magnetic field strengths.
For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.
A state of a system at higher energy than the ground state.
A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.
The study of which frequencies of radiation are absorbed or emitted by a particular substance and the correlation of these frequencies with details of molecular structure.
Triglycerides that are liquids at room temperature.
A chemical entity with an unpaired electron.
retention of configuration
During a reaction, when the configuration of a chirality center remains unchanged.
A compound that contains no p bonds.
A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)
A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.