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Solutions for Chapter 22.5SE: 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 22.5SE

Solutions for Chapter 22.5SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 22.5SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 22.5SE have been answered, more than 66104 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • anomers

    Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.

  • band theory.

    Delocalized electrons move freely through “bands” formed by overlapping molecular orbitals. (21.3)

  • chromatogram

    In gas chromatography, a plot that identifies the retention time of each compound in the mixture.

  • conjugated

    A compound in which two p bonds are separated from each other by exactly one s bond.

  • Cycloalkane

    A saturated hydrocarbon that contains carbons joined to form a ring

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • electrophoresis

    A technique for separating amino acids from each other based on a difference in pI values.

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Ground state

    The lowest energy state of a system.

  • halogenation

    A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.

  • localized lone pair

    A lone pair thatis not participating in resonance.

  • Molecular orbital (MO) theory

    A theory of chemical bonding in which electrons in molecules occupy molecular orbitals that extend over the entire molecule and are formed by the combination of the atomic orbitals that make up the molecule

  • nuclear binding energy

    The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)

  • polynucleotide

    A polymer constructed from nucleotides linked together.

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • Principle of microscopic reversibility

    This principle states that the sequence of transition states and reactive intermediates in the mechanism of any reversible reaction must be the same, but in reverse order, for the reverse reaction as for the forward reaction

  • qualitative analysis

    The determination of the presence or absence of a particular substance in a mixture. (Section 17.7)

  • Stereoselective reaction

    A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.

Textbook Survival Guides

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