Solutions for Chapter 2.14SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 2.14SE

Solutions for Chapter 2.14SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 2.14SE have been answered, more than 107594 students have viewed full step-by-step solutions from this chapter. Chapter 2.14SE includes 2 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: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • autocatalytic

    A reaction for which the reagent necessary to catalyze the reaction is produced by the reaction itself.

  • buffered solution (buffer)

    A solution that undergoes a limited change in pH upon addition of a small amount of acid or base. (Section 17.2)

  • catalyst

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

  • column chromatography

    A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.

  • coplanar

    Atoms that lie in the same plane.

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • Dalton’s law of partial pressures.

    The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)

  • deshielded

    In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is poor.

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • haloform reaction

    A reaction in which a methyl ketone is converted into a carboxylic acid upon treatment with excess base and excess halogen, followed by aqueous acid.

  • hydrazone

    A compound with the structure R2CRN!NH2.

  • induction

    The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.

  • octet rule

    A rule stating that bonded atoms tend to possess or share a total of eight valence-shell electrons. (Section 8.1)

  • parent ion

    In mass spectrometry,the ion that is generated when the compound is ionized.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • propagation

    For radical reactions,the steps whose sum gives the net chemical reaction.

  • R,S System

    A set of rules for specifying absolute confi guration about a chiral center; also called the Cahn-Ingold-Prelog system

  • rare earth element

    See lanthanide element. (Sections 6.8 and 6.9)

  • Stereocenter

    An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter

  • triglyceride

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

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