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Solutions for Chapter 15.10SE: 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 15.10SE

Solutions for Chapter 15.10SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 15.10SE have been answered, more than 66481 students have viewed full step-by-step solutions from this chapter. Chapter 15.10SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • band

    An array of closely spaced molecular orbitals occupying a discrete range of energy. (Section 12.4)

  • base peak

    In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.

  • bonding molecular orbital.

    A molecular orbital that is of lower energy and greater stability than the atomic orbitals from which it was formed. (10.6)

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • configuration

    The 3D spatial orientation of the groups connected to a chirality center (R or S ) or of the groups in a stereoisiomeric alkene (E or Z).

  • d-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the right.

  • Dextrorotatory

    Refers to a substance that rotates the plane of polarized light to the right

  • equilibrium constant

    The numerical value of the equilibrium-constant expression for a system at equilibrium. The equilibrium constant is most usually denoted by Kp for gas-phase systems or Kc for solution-phase systems. (Section 15.2)

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • Newman projection

    A way to view a molecule by looking along a carbon-carbon single bond

  • nucleophilic attack

    One of the four arrow-pushing patterns for ionic reactions.

  • Nucleophilic substitution

    Any reaction in which one nucleophile is substituted for another at a tetravalent carbon atom.

  • Photodynamic therapy

    Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.

  • solute

    A substance dissolved in a solvent to form a solution; it is normally the component of a solution present in the smaller amount. (Section 4.1)

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • Trans

    A prefi x meaning across from.

  • wavenumber

    In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.

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