Solutions for Chapter 15.7SE: 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 15.7SE

Solutions for Chapter 15.7SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 15.7SE have been answered, more than 145590 students have viewed full step-by-step solutions from this chapter. Chapter 15.7SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

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

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

  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • amino acid

    A carboxylic acid that contains an amino 1¬NH22 group attached to the carbon atom adjacent to the carboxylic acid 1¬COOH2 functional group. (Section 24.7)

  • bonding MO

    A low-energy molecular orbital resulting from the constructive interference between atomic orbitals.

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • endothermic

    Any process with a positive DH (the system receives energy from the surroundings).

  • hydroperoxide

    A compound with the structure R!O!O!H.

  • hydroxyl group

    An OH group.

  • molecular solids

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

  • net ionic equation

    A chemical equation for a solution reaction in which soluble strong electrolytes are written as ions and spectator ions are omitted. (Section 4.2)

  • nucleotides

    The product formed when a nucleoside is coupled to a phosphate group

  • Oligosaccharide

    A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.

  • Primary structure of nucleic acids

    The sequence of bases along the pentose-phosphodiester backbone of a DNA or RNA molecule read from the 5’ end to the 3’ end

  • protium

    The most common isotope of hydrogen. (Section 22.2)

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • sterically hindered

    A compound or region of a compound that is very bulky.

  • van der Waals forces

    A group of intermolecular attractive forces including dipole-dipole, dipole-induced dipole, and induced dipole-induced dipole (dispersion) forces

  • Vicinal coupling

    a !CH"CH2 group

  • Wittig reagent

    A reagent used to perform a Wittig reaction.

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

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