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Solutions for Chapter 19.1SE: 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 19.1SE

Solutions for Chapter 19.1SE
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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 19.1SE includes 2 full step-by-step solutions. Since 2 problems in chapter 19.1SE have been answered, more than 245299 students have viewed full step-by-step solutions from this chapter.

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

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

  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • anode.

    The electrode at which oxidation occurs. (18.2)

  • anti-periplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of approximately 180°.

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • aqueous solution.

    A solution in which the solvent is water. (4.1)

  • chiral.

    Compounds or ions that are not superimposable with their mirror images. (23.4)

  • compound.

    A substance composed of atoms of two or more elements chemically united in fixed proportions. (1.4)

  • continuous-wave (CW) spectrometer

    An NMR spectrometer that holds the magnetic field constant and slowly sweeps through a range of rf frequencies, monitoring which frequencies are absorbed.

  • d-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the right.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • intermolecular forces

    The short-range attractive forces operating between the particles that make up the units of a liquid or solid substance. These same forces also cause gases to liquefy or solidify at low temperatures and high pressures. (Chapter 11: Introduction)

  • Ketose

    A monosaccharide containing a ketone group.

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • Oxidative addition

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

  • 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.

  • R,S System

    A set of rules for specifying absolute confi guration about a chiral center; also called the Cahn-Ingold-Prelog system

  • Reductive amination

    A method for preparing substituted amines by treating an aldehyde or ketone with an amine in the presence of a reducing agent

  • spin-spin splitting

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms, in which the multiplicity of each signal is affected by the other.

  • Triol

    A compound containing three hydroxyl groups.

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