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Solutions for Chapter Chapter 50: Sample Preparation

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 50: Sample Preparation

Solutions for Chapter Chapter 50
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Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. Chapter Chapter 50: Sample Preparation includes 1 full step-by-step solutions. Since 1 problems in chapter Chapter 50: Sample Preparation have been answered, more than 46231 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions.

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

    An alloy of mercury with another metal or metals. (21.2)

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • biodegradable

    Organic material that bacteria are able to oxidize. (Section 18.4)

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • chlorofluorocarbons (CFCs)

    Compound containing only carbon, chlorine, and fluorine.

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • Gilman reagent

    A lithium dialkyl cuprate (R2CuLi).

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • inversion of configuration

    During a reaction, when the configuration of a chirality center is changed.

  • Lewis acid

    A compound capable offunctioning as an electron pair acceptor.

  • Mass spectrometry

    An analytical technique for measuring the mass-to-charge ratio (m/z) of ions.

  • Ostwald process

    An industrial process used to make nitric acid from ammonia. The NH3 is catalytically oxidized by O2 to form NO; NO in air is oxidized to NO2; HNO3 is formed in a disproportionation reaction when NO2 dissolves in water. (Section 22.7)

  • phospholipids

    Esterlike derivatives of phosphoric acid.

  • Secondary structure of proteins

    The ordered arrangements (conformations) of amino acids in localized regions of a polypeptide or protein

  • specific rotation

    For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.

  • transport protein

    A protein used to transport molecules or ions from one location to another. Hemoglobin is a classic example of a transport protein, used to transport molecular oxygen from the lungs to all the tissues of the body.

  • Valence shell

    The outermost occupied electron shell of an atom.

  • weak deactivators

    Groups that weakly deactivate an aromatic ring toward electrophilic aromatic substitution, thereby decreasing the rate of the reaction.

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