Solutions for Chapter 4.15SE: 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 4.15SE

Solutions for Chapter 4.15SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 4.15SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 4.15SE have been answered, more than 148594 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • (n 1 1) rule

    If a hydrogen has n hydrogens nonequivalent to it but equivalent among themselves on the same or adjacent atom(s), its 1 H!NMR signal is split into (n 1 1) peaks

  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • amphiprotic

    Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)

  • atomic number

    The number of protons in the nucleus of an atom of an element. (Section 2.3)

  • azo dyes

    A class of colored compounds that are formed via azo coupling.

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • Brønsted-Lowry base

    A compound that can serve as a proton acceptor.

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • dextrorotatory

    A compound that rotates plane-polarized light in a clockwise direction (+).

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • Friedel-Crafts reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • Hund’s rule

    When considering electrons in atomic orbitals, a rule that states that one electron is placed in each degenerate orbital first, before electrons are paired up.

  • mercapto group

    An SH group.

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • Pro-S-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an S confi guration

  • sigma 1S2 bond

    A covalent bond in which electron density is concentrated along the internuclear axis. (Section 9.6)

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • Transesterifi cation

    Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

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