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Solutions for Chapter 17.12SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 17.12SE

Solutions for Chapter 17.12SE
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Chapter 17.12SE includes 2 full step-by-step solutions. 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. Since 2 problems in chapter 17.12SE have been answered, more than 262514 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
  • carbonyl group

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

  • chemical shift (d)

    In an NMR spectrum, the location of a signal, defined relative to the frequency of absorption of a reference compound, tetramethylsilane (TMS).

  • chlorofluorocarbons

    Compounds composed entirely of chlorine, fluorine, and carbon. (Section 18.3)

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • glucose

    A polyhydroxy aldehyde whose formula is CH2OH1CHOH24CHO; it is the most important of the monosaccharides. (Section 24.8)

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • Line-angle formula

    An abbreviated way to draw structural formulas in which vertices and line endings represent carbons

  • molal boiling-point-elevation constant (Kb)

    A constant characteristic of a particular solvent that gives the increase in boiling point as a function of solution molality: ?Tb = Kbm. (Section 13.5)

  • molecular solids

    Solids that are composed of molecules. (Sections 12.1 and 12.6)

  • peptide bond

    A bond formed between two amino acids. (Section 24.7)

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • solute

    A substance dissolved in a solvent to form a solution; it is normally the component of a solution present in the smaller amount. (Section 4.1)

  • Williamson ether synthesis

    A general method for the synthesis of dialkyl ethers by an SN2 reaction between a haloalkane and an alkoxide ion.

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