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Solutions for Chapter 1.5SE: 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 1.5SE

Solutions for Chapter 1.5SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 1.5SE have been answered, more than 66938 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 1.5SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • atomic number (Z).

    The number of protons in the nucleus of an atom. (2.3)

  • Atropisomers

    Enantiomers that lack a chiral center and differ because of hindered rotation.

  • axial position

    For chair conformations of substituted cyclohexanes, a position that is parallel to a vertical axis passing through the center of the ring.

  • chemical formula

    A notation that uses chemical symbols with numerical subscripts to convey the relative proportions of atoms of the different elements in a substance. (Section 2.6)

  • continuous spectrum

    A spectrum that contains radiation distributed over all wavelengths. (Section 6.3)

  • crown ether

    Cyclic polyethers whose molecular models resemble crowns.

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • electron-domain geometry

    The three- dimensional arrangement of the electron domains around an atom according to the VSEPR model. (Section 9.2)

  • functional group

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

  • half-reaction

    An equation for either an oxidation or a reduction that explicitly shows the electrons involved, for example, Zn2 + 1aq2 + 2 e- ¡ Zn1s2. (Section 20.2)

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • high-resolution mass spectrometry

    A technique that involves the use of a detector that can measure the m/z values to four decimal places.This technique allows for the determination of the molecular formula of an unknown compound.

  • Lipid bilayer

    A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.

  • mass spectrum

    In mass spectrometry,a plot that shows the relative abundance ofeach cation that was detected.

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • Ortho

    Refers to groups occupying l,2-positions on a benzene ring.

  • ortho-para director

    A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.

  • replacement test

    A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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