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Textbooks / Chemistry / General Chemistry: Principles and Modern Applications 10

General Chemistry: Principles and Modern Applications 10th Edition - Solutions by Chapter

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Full solutions for General Chemistry: Principles and Modern Applications | 10th Edition

ISBN: 9780132064521

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

General Chemistry: Principles and Modern Applications | 10th Edition - Solutions by Chapter

The full step-by-step solution to problem in General Chemistry: Principles and Modern Applications were answered by , our top Chemistry solution expert on 12/23/17, 04:52PM. General Chemistry: Principles and Modern Applications was written by and is associated to the ISBN: 9780132064521. This expansive textbook survival guide covers the following chapters: 28. This textbook survival guide was created for the textbook: General Chemistry: Principles and Modern Applications, edition: 10. Since problems from 28 chapters in General Chemistry: Principles and Modern Applications have been answered, more than 83295 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • acid ionization constant (Ka).

    The equilibrium constant for the acid ionization. (15.5)

  • aliphatic hydrocarbons.

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

  • alkylthio group

    An SR group.

  • annulenes

    Compounds consisting of a single ring containing a fully conjugated p system. Benzene is [6]annulene.

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • density

    The ratio of an object’s mass to its volume. (Section 1.4)

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • enantiomers

    Two mirror-image molecules of a chiral substance. The enantiomers are nonsuperimposable. (Section 23.4)

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • extensive property

    A property that depends on the amount of material considered; for example, mass or volume. (Section 1.3)

  • Grignard reagent

    A carbanion with the structure RMgX.

  • halogenation

    A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.

  • Heterocycle

    A cyclic compound whose ring contains more than one kind of atom. Oxirane (ethylene oxide), for example, is a heterocycle whose ring contains two carbon atoms and one oxygen atom.

  • joule (J)

    The SI unit of energy, 1 kg@m2 >s2. A related unit is the calorie: 4.184 J = 1 cal. (Section 5.1)

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • Photodynamic therapy

    Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.