Solutions for Chapter 2.9SE: 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 2.9SE

Solutions for Chapter 2.9SE
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This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 2.9SE have been answered, more than 108704 students have viewed full step-by-step solutions from this chapter. Chapter 2.9SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • acidic anhydride (acidic oxide)

    An oxide that forms an acid when added to water; soluble nonmetal oxides are acidic anhydrides. (Section 22.5)

  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • alkynes

    Compounds containing a carbon-carbon triple bond.

  • alpha (a) rays.

    Helium ions with a positive charge of 12. (2.2)

  • amine

    Compounds containing a nitrogen atom that is connected to one, two, or three alkyl or aryl groups.

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • Chain propagation

    A step in a chain reaction characterized by the reaction of a reactive intermediate and a molecule to give a new reactive intermediate and a new molecule.

  • Cyanohydrin

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

  • disrotatory

    In electrocyclicreactions, a type of rotation in which the orbitalsbeing used to form the new s bond must rotate in opposite directions (one rotates clockwise while the other rotates counterclockwise).

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • Enolate anion

    An anion derived by loss of a hydrogen from a carbon alpha to a carbonyl group; the anion of an enol.

  • formal charge

    The number of valence electrons in an isolated atom minus the number of electrons assigned to the atom in the Lewis structure. (Section 8.5)

  • orbital

    An allowed energy state of an electron in the quantum mechanical model of the atom; the term orbital is also used to describe the spatial distribution of the electron. An orbital is defined by the values of three quantum numbers: n, l, and ml (Section 6.5)

  • Polynuclear aromatic hydrocarbon (PAH)

    A hydrocarbon containing two or more fused benzene rings

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

  • spectrum

    The distribution among various wavelengths of the radiant energy emitted or absorbed by an object. (Section 6.3)

  • Thermodynamic control

    Experimental conditions that permit the establishment of equilibrium between two or more products of a reaction. The composition of the product mixture is determined by the relative stabilities of the products.

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