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Solutions for Chapter 10.7SE: 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 10.7SE

Solutions for Chapter 10.7SE
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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 10.7SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 10.7SE have been answered, more than 66111 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkynide ion

    The conjugate base of a terminal alkyne.

  • allotropes.

    Two or more forms of the same element that differ significantly in chemical and physical properties. (2.6)

  • Allylic carbon

    A carbon adjacent to a carbon-carbon double bond.

  • atmosphere (atm)

    A unit of pressure equal to 760 torr; 1 atm = 101.325 kPa. (Section 10.2) atom The smallest representative particle of an element. (Sections 1.1 and 2.1)

  • Carbocation

    A species in which a carbon atom has only six electrons in its valence shell and bears a positive charge

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • endothermic

    Any process with a positive DH (the system receives energy from the surroundings).

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • Hydrogen bonding

    The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • Imine

    A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base

  • isolated diene

    A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • polycarbonates

    Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons

  • Polynuclear aromatic hydrocarbon (PAH)

    A hydrocarbon containing two or more fused benzene rings

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • regioselective

    A reaction that can produce two or more constitutional isomers but nevertheless produces one as the major product.

  • stereoisomers

    Compounds that have the same constitution but differ in the 3D arrangement of atoms.

  • thiols

    Compounds containing a mercapto group (SH).

Textbook Survival Guides

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