Solutions for Chapter 2.1SE: 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 2.1SE

Solutions for Chapter 2.1SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 2.1SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 2.1SE have been answered, more than 146008 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • aldose

    A carbohydrate that contains an aldehyde group.

  • Annulene

    A cyclic hydrocarbon with a continuous alternation of single and double bonds.

  • anomers

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

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • cellulose

    A polysaccharide of glucose; it is the major structural element in plant matter. (Section 24.8)

  • chlorofluorocarbons

    Compounds composed entirely of chlorine, fluorine, and carbon. (Section 18.3)

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • conjugate acid–base pair

    An acid and a base, such as H2O and OH-, that differ only in the presence or absence of a proton. (Section 16.2)

  • conrotatory

    In electrocyclic reactions,a type of rotation in which the orbitals being used to form the new s bond must rotate in the same way.

  • corrosion.

    The deterioration of metals by an electrochemical process. (18.7)

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • lattice energy

    The energy required to separate completely the ions in an ionic solid. (Section 8.2)

  • N-glycoside

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

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • SN2 reaction

    A bimolecular nucleophilic substitution reaction.

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

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