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Solutions for Chapter 10.2SE: 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 10.2SE

Solutions for Chapter 10.2SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 10.2SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 10.2SE have been answered, more than 66104 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alpha (a) amino acid

    A compound containing a carboxylic acid group (COOH) as well as an amino group (NH2), both of which are attached to the same carbon atom.

  • Anabolic steroid

    A steroid hormone, such as testosterone, that promotes tissue and muscle growth and development

  • annulenes

    Compounds consisting of a single ring containing a fully conjugated p system. Benzene is [6]annulene.

  • biodegradable

    Organic material that bacteria are able to oxidize. (Section 18.4)

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • E1

    A unimolecular b-elimination reaction

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • Gabriel synthesis

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

  • heterocycle

    A cyclic compound containing at least one heteroatom (such as S, N, or O) in the ring.

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • instantaneous rate

    The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

  • intermolecular forces

    The short-range attractive forces operating between the particles that make up the units of a liquid or solid substance. These same forces also cause gases to liquefy or solidify at low temperatures and high pressures. (Chapter 11: Introduction)

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • parts per million (ppm)

    The concentration of a solution in grams of solute per 106 (million) grams of solution; equals milligrams of solute per liter of solution for aqueous solutions. (Section 13.4)

  • prostaglandins

    Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.

  • Reductive amination

    A method for preparing substituted amines by treating an aldehyde or ketone with an amine in the presence of a reducing agent

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • Restriction endonuclease

    An enzyme that catalyzes the hydrolysis of a particular phosphodiester bond within a DNA strand.

  • VSEPR theory

    Valence Shell Electron Pair Repulsion theory, which can be used to predict the geometry around an atom.

Textbook Survival Guides

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