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Solutions for Chapter 16.1SE: 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 16.1SE

Solutions for Chapter 16.1SE
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Since 2 problems in chapter 16.1SE have been answered, more than 265799 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 16.1SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,3-diaxial interaction

    Steric interactions that occur between axial substituents in a chair conformation.

  • absorption spectrum

    A pattern of variation in the amount of light absorbed by a sample as a function of wavelength. (Section 23.5)

  • acid-catalyzed hydration

    A reaction that achieves the addition of water across a double bond in the presence of an acid catalyst.

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • atomic orbital.

    The wave function (?) of an electron in an atom. (7.5)

  • 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)

  • b-Elimination

    A reaction in which a molecule, such as HCl, HBr, HI, or HOH, is split out or eliminated from adjacent carbons

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • biodegradable polymers

    Polymers that can be broken down by enzymes produced by soil microorganisms.

  • C-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !COOH group.

  • Dalton’s law of partial pressures.

    The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)

  • ether

    A compound in which two hydrocarbon groups are bonded to one oxygen. (Section 24.4)

  • hydrazone

    A compound with the structure R2CRN!NH2.

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • hydrogen bonding

    Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)

  • hydroperoxide

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

  • molecular solids

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

  • nomenclature

    A system for naming organic compounds.

  • rate constant

    A constant of proportionality between the reaction rate and the concentrations of reactants that appear in the rate law. (Section 14.3)

  • stereoselective

    A reaction in which one substrate produces two stereoisomers in unequal amounts.