Solutions for Chapter 5.7SE: 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 5.7SE

Solutions for Chapter 5.7SE
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Since 2 problems in chapter 5.7SE have been answered, more than 146716 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 5.7SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

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

    The product obtainedfrom 1,2-addition across a conjugated p system.

  • acyl peroxide

    A peroxide for which each oxygen atom is connected to an acyl group. Acyl peroxides are often used as radical initiators, because the O!O bond is especially weak.

  • Angle strain

    The strain that arises when a bond angle is either compressed or expanded compared to its optimal value.

  • Avogadro’s number (NA)

    The number of 12C atoms in exactly 12 g of 12C; it equals 6.022 * 1023 mol-1. (Section 3.4)

  • bidentate ligand

    A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)

  • concentration of a solution.

    The amount of solute present in a given quantity of solvent or solution. (4.5)

  • Diels-Alder adduct

    A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.

  • displacement reaction

    A reaction in which an element reacts with a compound, displacing an element from it. (Section 4.4)

  • Hammond’s postulate

    The structure of the transition state for an exothermic step looks more like the reactants of that step than the products. Conversely, the structure of the transition state for an endothermic step looks more like the products of that step than the reactants.

  • Ketose

    A monosaccharide containing a ketone group.

  • Lactone

    A cyclic ester.

  • Messenger RNA (mRNA)

    A ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins

  • ortho

    On an aromatic ring, the C2 position.

  • phase diagram

    A graphic representation of the equilibria among the solid, liquid, and gaseous phases of a substance as a function of temperature and pressure. (Section 11.6)

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • secondary

    A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).

  • semiconductor

    A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)

  • solvolysis

    A substitution reaction in which the solvent functions as the nucleophile.

  • thiolate

    The conjugate base of a thiol.

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