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 21081 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • back-side attack

    In SN2 reactions, the side opposite the leaving group, which is where the nucleophile attacks.

  • breeder reactor.

    A nuclear reactor that produces more fissionable materials than it uses. (19.5)

  • chair conformation

    The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered.

  • density.

    The mass of a substance divided by its volume. (1.6)

  • elastomers

    Polymers that return to their original shape after being stretched.

  • frequency

    For electromagnetic radiation, the number of wavelengths that pass a particular point in space per unit time.

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • molecular equation

    A chemical equation in which the formula for each substance is written without regard for whether it is an electrolyte or a nonelectrolyte. (Section 4.2)

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • N-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !NH2 group

  • nucleus

    The very small, very dense, positively charged portion of an atom; it is composed of protons and neutrons. (Section 2.2)

  • Oil

    When used in the context of fats and oils, a mixture of triglycerides that is liquid at room temperature

  • Oxidative addition

    Addition of a reagent to a metal center causing it to add two substituents and to increase its oxidation state by two

  • periodic table

    The arrangement of elements in order of increasing atomic number, with elements having similar properties placed in vertical columns. (Section 2.5)

  • polar aprotic solvent

    A solvent that lacks hydrogen atoms connected directly to an electronegative atom.

  • retention of configuration

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

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

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