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Solutions for Chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONS

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONS

Solutions for Chapter 16.17
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Since 1 problems in chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONS have been answered, more than 38434 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 16.17: THE GENERAL MECHANISM FOR NUCLEOPHILIC ADDITIONAL - ELIMINATION REACTIONS includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • Activating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.

  • battery.

    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)

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • chiral

    A term describing a molecule or an ion that cannot be superimposed on its mirror image. (Sections 23.4 and 24.5)

  • Circular DNA

    A type of double-stranded DNA in which the 59 and 39 ends of each strand are joined by phosphodiester groups.

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • Cycloaddition reaction

    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

  • diamagnetic anisotropy

    An effect that causes different regions of space to be characterized by different magnetic field strengths.

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • Excited state

    A state of a system at higher energy than the ground state.

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • Molecular spectroscopy

    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.

  • oils

    Triglycerides that are liquids at room temperature.

  • radical

    A chemical entity with an unpaired electron.

  • retention of configuration

    During a reaction, when the configuration of a chirality center remains unchanged.

  • saturated

    A compound that contains no p bonds.

  • semiconductor

    A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)

  • soluble

    A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.

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