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Solutions for Chapter 17.16SE: 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 17.16SE

Solutions for Chapter 17.16SE
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Since 2 problems in chapter 17.16SE have been answered, more than 237059 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. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 17.16SE 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
  • adsorption

    The binding of molecules to a surface. (Section 14.7)

  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • bonding molecular orbital

    A molecular orbital in which the electron density is concentrated in the internuclear region. The energy of a bonding molecular orbital is lower than the energy of the separate atomic orbitals from which it forms. (Section 9.7)

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • conjugate acid–base pair

    An acid and a base, such as H2O and OH-, that differ only in the presence or absence of a proton. (Section 16.2)

  • conrotatory

    In electrocyclic reactions,a type of rotation in which the orbitals being used to form the new s bond must rotate in the same way.

  • Cycloaddition reaction

    A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction

  • dipole–dipole force

    A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • fracking

    The practice in which water laden with sand and other materials is pumped at high pressure into rock formations to release natural gas and other petroleum materials. (Section 18.4)

  • Frost circles

    A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.

  • 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.

  • kinetic energy

    The energy that an object possesses by virtue of its motion. (Section 5.1)

  • Oxidative addition

    Addition of a reagent to a metal center causing it to add two substituents and to increase its oxidation state by two

  • Protecting group

    Reversibly creating an unreactive group for the purpose of preventing a functional group from potentially reacting to give an unwanted product or products

  • Reductive elimination

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

  • Upfield

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

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