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Solutions for Chapter 22: Carbonyl Alpha-Substitution Reactions

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9781305080485

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Solutions for Chapter 22: Carbonyl Alpha-Substitution Reactions

Solutions for Chapter 22
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Textbook: Organic Chemistry
Edition: 9
Author: John E. McMurry
ISBN: 9781305080485

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Chapter 22: Carbonyl Alpha-Substitution Reactions includes 69 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781305080485. Since 69 problems in chapter 22: Carbonyl Alpha-Substitution Reactions have been answered, more than 15239 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • accuracy

    A measure of how closely individual measurements agree with the correct value. (Section 1.5)

  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • Benzyne intermediate

    A reactive intermediate formed by b-elimination from adjacent carbon atoms of a benzene ring and having a triple bond in the benzene ring. The second p bond of the benzyne triple bond is formed by the weak overlap of coplanar 2p orbitals on adjacent carbons.

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • chiral

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

  • corrosion.

    The deterioration of metals by an electrochemical process. (18.7)

  • Coupling constant

    The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.

  • Diastereomers

    Stereoisomers that are not mirror images of each other; refers to relationships among two or more objects

  • diffusion

    The spreading of one substance through a space occupied by one or more other substances. (Section 10.8)

  • dilution.

    A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • hydrogen bonding

    A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • solubility

    The amount of a substance that dissolves in a given quantity of solvent at a given temperature to form a saturated solution. (Sections 4.2 and 13.2)

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

  • triplet

    In NMR spectroscopy, a signal that is comprised of three peaks.

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

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