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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 38242 students have viewed full step-by-step answer.

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

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • alkanamine

    A format for naming primary amines containing a complex alkyl group.

  • atomic number (Z).

    The number of protons in the nucleus of an atom. (2.3)

  • atomic orbital.

    The wave function (?) of an electron in an atom. (7.5)

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • cation.

    An ion with a net positive charge. (2.5)

  • chiral

    An object that is not superimposable on its mirror image.

  • Cis, trans isomers

    Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.

  • cubic close packing

    A crystal structure where the atoms are packed together as close as possible, and the close-packed layers of atoms adopt a three-layer repeating pattern that leads to a face-centered cubic unit cell. (Section 12.3)

  • Functional group

    An atom or group of atoms within a molecule that shows a characteristic set of physical and chemical properties

  • halogenation

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

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • Molecular spectroscopy

    The study of which frequencies of radiation are absorbed or emitted by a particular substance and the correlation of these frequencies with details of molecular structure.

  • neutron

    An electrically neutral particle found in the nucleus of an atom; it has approximately the same mass as a proton. (Section 2.3)

  • overlap

    The extent to which atomic orbitals on different atoms share the same region of space. When the overlap between two orbitals is large, a strong bond may be formed. (Section 9.4)

  • Plane-polarized light

    Light oscillating in only parallel planes.

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • Spin-spin coupling

    An interaction in which nuclear spins of adjacent atoms infl uence each other and lead to the spitting of NMR signals.

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