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Solutions for Chapter Chapter 25: Chromatographic Methods and Capillary Electrophoresis

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Full solutions for Quantitative Chemical Analysis | 8th Edition

ISBN: 9781429218153

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Solutions for Chapter Chapter 25: Chromatographic Methods and Capillary Electrophoresis

Solutions for Chapter Chapter 25
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Textbook: Quantitative Chemical Analysis
Edition: 8
Author: Daniel C. Harris
ISBN: 9781429218153

This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8. Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. Since 51 problems in chapter Chapter 25: Chromatographic Methods and Capillary Electrophoresis have been answered, more than 49315 students have viewed full step-by-step solutions from this chapter. Chapter Chapter 25: Chromatographic Methods and Capillary Electrophoresis includes 51 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

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

    Attraction between unlike molecules. (11.3)

  • alkoxy substituent

    An OR group.

  • anti-periplanar

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

  • asymmetric stretching

    In IR spectroscopy, when two bonds are stretching out of phase with each other.

  • back-side attack

    In SN2 reactions, the side opposite the leaving group, which is where the nucleophile attacks.

  • chemical equation.

    An equation that uses chemical symbols to show what happens during a chemical reaction. (3.7)

  • dextrorotatory, or merely dextro or d

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the right (clockwise). (Section 23.4)

  • diborane

    B2H6. A dimeric structure formed when one borane molecule reacts with another.

  • E (Section 5.2C)

    From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • induction

    The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.

  • insulators

    Materials that do not conduct electricity. (Section 12.7)

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • kinetic control

    A reaction for which the product distribution is determined by the relative rates at which the products are formed.

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • polyether

    A compound containing several ether groups.

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

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