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Solutions for Chapter 6: Chemical Reactivity and Mechanisms

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Solutions for Chapter 6: Chemical Reactivity and Mechanisms

Solutions for Chapter 6
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

Chapter 6: Chemical Reactivity and Mechanisms includes 64 full step-by-step solutions. Since 64 problems in chapter 6: Chemical Reactivity and Mechanisms have been answered, more than 146235 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition reactions

    Reactions that are characterized by the addition of two groups across a double bond. In the process, the pi (p) bond is broken.

  • alkyl group

    A substituent lacking p bonds and comprised of only carbon and hydrogen atoms.

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • amino acids.

    A compound that contains at least one amino group and at least one carboxyl group. (25.3)

  • amphiprotic

    Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • catalyst

    A substance that changes the speed of a chemical reaction without itself undergoing a permanent chemical change in the process. (Section 14.7)

  • desalination

    The removal of salts from seawater, brine, or brackish water to make it fit for human consumption. (Section 18.4)

  • electrolyte

    A solute that produces ions in solution; an electrolytic solution conducts an electric current. (Section 4.1)

  • elemental semiconductor

    A semiconducting material composed of just one element. (Section 12.7)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • magic numbers

    Numbers of protons and neutrons that result in very stable nuclei. (Section 21.2)

  • main-group elements

    Elements in the s and p blocks of the periodic table. (Section 6.9)

  • net ionic equation

    A chemical equation for a solution reaction in which soluble strong electrolytes are written as ions and spectator ions are omitted. (Section 4.2)

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • Transfer RNA (tRNA

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

  • triglyceride

    A triester formed from glycerol and three long-chain carboxylic acids.

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.