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Textbooks / Chemistry / Student Solutions Manual for Physical Chemistry 10

Student Solutions Manual for Physical Chemistry 10th Edition Solutions

Do I need to buy Student Solutions Manual for Physical Chemistry | 10th Edition to pass the class?

ISBN: 9781464124495

Student Solutions Manual for Physical Chemistry | 10th Edition - Solutions by Chapter

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Textbook: Student Solutions Manual for Physical Chemistry
Edition: 10
Author: Charles Trapp; Carmen Giunta; Marshall Cady
ISBN: 9781464124495

The full step-by-step solution to problem in Student Solutions Manual for Physical Chemistry were answered by , our top Chemistry solution expert on 10/03/18, 06:29PM. Since problems from 0 chapters in Student Solutions Manual for Physical Chemistry have been answered, more than 200 students have viewed full step-by-step answer. Student Solutions Manual for Physical Chemistry was written by and is associated to the ISBN: 9781464124495. This expansive textbook survival guide covers the following chapters: 0. This textbook survival guide was created for the textbook: Student Solutions Manual for Physical Chemistry, edition: 10.

Key Chemistry Terms and definitions covered in this textbook
  • Allene

    The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.

  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • anti-Markovnikov addition

    An addition reaction in which a hydrogen atom is installed at the more substituted vinylic position and another group (such as a halogen) is installed at the less substituted vinylic position.

  • Avogadro’s law.

    At constant pressure and temperature, the volume of a gas is directly proportional to the number of moles of the gas present. (5.3)

  • basic oxide (basic anhydride)

    An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • Carbocation

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

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • electronegativity

    A measure of the ability of an atom that is bonded to another atom to attract electrons to itself. (Section 8.4)

  • Fischer esterifi cation

    The process of forming an ester by refl uxing a carboxylic acid and an alcohol in the presence of an acid catalyst, commonly H2SO4, ArSO3H, or HCl

  • Gibbs free energy change (DG°)

    The energy that dictates the position of chemical equilibria and rates of chemical reactions. A thermodynamic function of enthalpy, entropy, and temperature, given by the equation DG° 5 DH° 2 TDS°. If DG° , 0, the position of equilibria for the reaction favors products. If DG° . 0, the position of equilibria favors reactants.

  • glycoside

    An acetal that is obtained by treating the cyclic hemiacetal form of a monosaccharide with an alcohol under acid-catalyzed conditions.

  • neutralization reaction

    A reaction in which an acid and a base react in stoichiometrically equivalent amounts; the neutralization reaction between an acid and a metal hydroxide produces water and a salt. (Section 4.3)

  • 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.

  • saturated

    A compound that contains no p bonds.

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • Strecker synthesis

    A synthetictechnique for preparing racemic a-amino acidsfrom aldehydes.