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Solutions for Chapter 16.16SE: 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 16.16SE

Solutions for Chapter 16.16SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 16.16SE have been answered, more than 67719 students have viewed full step-by-step solutions from this chapter. Chapter 16.16SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acetylide ion

    The conjugate base of acetylene or any terminal alkyne.

  • acidic anhydride (acidic oxide)

    An oxide that forms an acid when added to water; soluble nonmetal oxides are acidic anhydrides. (Section 22.5)

  • amorphous solid.

    A solid that lacks a regular three-dimensional arrangement of atoms or molecules. (11.7)

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • azo coupling

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

  • boiling-point elevation (DTb).

    The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)

  • carbonyl group

    A CRO bond. carboxylic acid derivative (Sect. 21.6): A compound that is similar in structure to a carboxylic acid (RCOOH) but the OH group of the carboxylic acid has been replaced with a different group, Z, where Z is a heteroatom such as Cl, O, N, etc. Nitriles (R!C#N) are also considered to be carboxylic acid derivatives because they have the same oxidation state as carboxylic acids.

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • Equivalent hydrogens

    Hydrogens that have the same chemical environment

  • fossil fuels

    Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)

  • Haber process

    The catalyst system and conditions of temperature and pressure developed by Fritz Haber and coworkers for the formation of NH3 from H2 and N2. (Section 15.2)

  • Hofmann product

    The less substituted product (alkene) of an elimination reaction.

  • ion-product constant

    For water, Kw is the product of the aquated hydrogen ion and hydroxide ion concentrations: 3H+43OH-4 = Kw = 1.0 * 10-14 at 25 °C. (Section 16.3)

  • Ka

    A measure of the strength of an acid: Ka = Keq 3H2O4 = 3H3O+ 4 3A- 4 3HA4

  • loss of a leaving group

    One of the four arrow-pushing patterns for ionic reactions.

  • mole

    A collection of Avogadro’s number 16.022 * 10232 of objects; for example, a mole of H2O is 6.022 * 1023 H2O molecules. (Section 3.4)

  • Polypeptide

    A macromolecule containing many amino acid units, each joined to the next by a peptide bond

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • Robinson annulation

    The combination of a Michael addition followed by an aldol condensation to form a ring.

Textbook Survival Guides

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