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Solutions for Chapter Chapter 42: 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 42: Sample Preparation

Solutions for Chapter Chapter 42
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter Chapter 42: Sample Preparation includes 1 full step-by-step solutions. Since 1 problems in chapter Chapter 42: Sample Preparation have been answered, more than 46177 students have viewed full step-by-step solutions from this chapter. Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • acetal

    A functional group characterized by two alkoxy (OR) groups connected to the same carbon atom.Acetals can be used as protecting groups for aldehydes or ketones.

  • alkanes.

    Hydrocarbons having the general formula CnH2n12, where n 5 1,2, . . . . (24.2)

  • androgens

    Male sex hormones.

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • band gap

    The energy gap between a fully occupied band called a valence band and an empty band called the conduction band. (Section 12.7)

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • Dielectric constant

    A measure of a solvent’s ability to insulate opposite charges from one another

  • electromotive force (emf)

    A measure of the driving force, or electrical pressure, for the completion of an electrochemical reaction. Electromotive force is measured in volts: 1 V = 1 J>C. Also called the cell potential. (Section 20.4)

  • enzymes

    Important biological molecules that catalyze virtually all cellular processes.

  • Homolytic bond cleavage

    Cleavage of a bond so that each fragment retains one electron; formation of radicals.

  • imidazole

    A compound containing a five-membered ring that is similar to pyrrole but has one extra nitrogen atom at the 3 position.

  • molecular weight

    The mass of the collection of atoms represented by the chemical formula for a molecule. (Section 3.3)

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • polysaccharide

    A substance made up of many monosaccharide units joined together. (Section 24.8)

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • Strecker synthesis

    A synthetictechnique for preparing racemic a-amino acidsfrom aldehydes.

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