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Solutions for Chapter 10.15SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 10.15SE

Solutions for Chapter 10.15SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 10.15SE includes 2 full step-by-step solutions. Since 2 problems in chapter 10.15SE have been answered, more than 246911 students have viewed full step-by-step solutions from this chapter. 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.

Key Chemistry Terms and definitions covered in this textbook
  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • aliphatic hydrocarbons.

    Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)

  • bond enthalpy.

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

  • Boyle’s law.

    The volume of a fixed amount of gas maintained at constant temperature is inversely proportional to the gas pressure. (5.3)

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • cathode.

    The electrode at which reduction occurs. (18.2)

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • chiral

    An object that is not superimposable on its mirror image.

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • cholesteric liquid crystalline phase

    A liquid crystal formed from flat, disc-shaped molecules that align through a stacking of the molecular discs. (Section 11.7)

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • crossed aldol reaction

    An aldol reaction that occurs between different partners.

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • diamagnetic.

    Repelled by a magnet; a diamagnetic substance contains only paired electrons. (7.8)

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • exergonic

    Any process with a negative DG.

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • hydrolysis

    A reaction in which bonds are cleaved by treatment with water.

  • internal energy

    The total energy possessed by a system. When a system undergoes a change, the change in internal energy, ?E, is defined as the heat, q, added to the system, plus the work, w, done on the system by its surroundings: ?E = q + w. (Section 5.2)

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