Solutions for Chapter 21: Amines

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 21: Amines

Solutions for Chapter 21
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Textbook: Organic Chemistry,
Edition: 9
Author: Francis A Carey Dr., Robert M. Giuliano
ISBN: 9780073402741

Since 40 problems in chapter 21: Amines have been answered, more than 10899 students have viewed full step-by-step solutions from this chapter. Chapter 21: Amines includes 40 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

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

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • alkyl amines

    A format for naming amines containing simple alkyl groups.

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • Cumulated

    A cumulated diene is one in which two double bonds share an sp-hybridized carbon

  • endothermic process

    A process in which a system absorbs heat from its surroundings. (Section 5.2)

  • Friedel-Crafts alkylation

    An electrophilic aromatic substitution reaction that installs an alkyl group on an aromatic ring.

  • Gabriel synthesis

    A method forpreparing primary amines that avoids formation of secondary and tertiary amines.

  • Lewis structure

    A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • Markovnikov’s rule

    In the addition of HX, H2O, or ROH to an alkene, hydrogen adds to the carbon of the double bond having the greater number of hydrogens.

  • pi 1P2 bond

    A covalent bond in which electron density is concentrated above and below the internuclear axis. (Section 9.6)

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.

  • reaction mechanism

    A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.

  • sigma (s) bond

    A bond that is characterized by circular symmetry with respect to the bond axis.

  • standard atmospheric pressure

    Defined as 760 torr or, in SI units, 101.325 kPa. (Section 10.2)

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • wavenumber

    In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.

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