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Solutions for Chapter 17.5SE: 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 17.5SE

Solutions for Chapter 17.5SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 17.5SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 17.5SE have been answered, more than 67409 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • amphiprotic

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

  • Avogadro’s law.

    At constant pressure and temperature, the volume of a gas is directly proportional to the number of moles of the gas present. (5.3)

  • base-dissociation constant (Kb)

    An equilibrium constant that expresses the extent to which a base reacts with solvent water, accepting a proton and forming OH-1aq2. (Section 16.7)

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • electron shell

    A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)

  • enolate

    The resonance-stabilized conjugate base of a ketone, aldehyde, or ester.

  • equilibrium-constant expression

    The expression that describes the relationship among the concentrations (or partial pressures) of the substances present in a system at equilibrium. The numerator is obtained by multiplying the concentrations of the substances on the product side of the equation, each raised to a power equal to its coefficient in the chemical equation. The denominator similarly contains the concentrations of the substances on the reactant side of the equation. (Section 15.2)

  • Gilman reagent

    A lithium dialkyl cuprate (R2CuLi).

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • Lewis acid

    A compound capable offunctioning as an electron pair acceptor.

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • Molecular ion (M1)

    The radical cation formed by removal of a single electron from a parent molecule in a mass spectrometer.

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • Nucleotide

    A nucleoside in which a molecule of phosphoric acid is esterifi ed with an !OH of the monosaccharide, most commonly either the 39!OH or the 59!OH.

  • reaction mechanism

    A detailed picture, or model, of how the reaction occurs; that is, the order in which bonds are broken and formed and the changes in relative positions of the atoms as the reaction proceeds. (Section 14.6)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • s-cis

    A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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