×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 19.7SE: 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 19.7SE

Solutions for Chapter 19.7SE
4 5 0 293 Reviews
11
0

Chapter 19.7SE includes 2 full step-by-step solutions. Since 2 problems in chapter 19.7SE have been answered, more than 262935 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. 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.

Key Chemistry Terms and definitions covered in this textbook
  • amines.

    Organic bases that have the functional group —NR2, where R may be H, an alkyl group, or an aromatic group. (24.4)

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • bond length.

    The distance between the nuclei of two bonded atoms in a molecule. (9.4)

  • Carbohydrate

    A polyhydroxyaldehyde, a polyhydroxyketone, or a substance that gives these compounds on hydrolysis.

  • chiral

    A term describing a molecule or an ion that cannot be superimposed on its mirror image. (Sections 23.4 and 24.5)

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • Frequency

    The number of full cycles of a wave that pass a given point in a second, and reported in hertz (Hz), which has the units s21

  • Friedel-Crafts alkylation

    An electrophilic aromatic substitution reaction that installs an alkyl group on an aromatic ring.

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • nonmetallic elements (nonmetals)

    Elements in the upper right corner of the periodic table; nonmetals differ from metals in their physical and chemical properties. (Section 2.5)

  • Pauli exclusion principle

    The rule that states that an atomic orbital or molecular orbital can accommodate a maximum of two electrons with opposite spin.

  • polymer

    A large molecule of high molecular mass, formed by the joining together, or polymerization, of a large number of molecules of low molecular mass. The individual molecules forming the polymer are called monomers. (Sections 12.1 and 12.8)

  • Primary structure of proteins

    The sequence of amino acids in the polypeptide chain, read from the N-terminal amino acid to the C-terminal amino acid.

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • simple lipid

    A lipid that does not undergo hydrolysis in aqueous acid or base to produce smaller fragments.

  • tetrahedral

    The geometry of an atom with four bonds separated from each other by 109.5°.

  • Tollens’ reagent

    A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.

  • upfield

    The right side of an NMRspectrum.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password