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Textbooks / Chemistry / Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card 3

Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card 3rd Edition Solutions

Do I need to buy Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card | 3rd Edition to pass the class?

ISBN: 9781337088299

Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card | 3rd Edition - Solutions by Chapter

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Textbook: Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card
Edition: 3
Author: Daniel L. Reger (Author), Scott R. Goode (Author), David W. Ball (Author)
ISBN: 9781337088299

Since problems from 0 chapters in Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card have been answered, more than 200 students have viewed full step-by-step answer. Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card was written by and is associated to the ISBN: 9781337088299. The full step-by-step solution to problem in Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card were answered by , our top Chemistry solution expert on 11/06/18, 07:54PM. This expansive textbook survival guide covers the following chapters: 0. This textbook survival guide was created for the textbook: Bundle: Chemistry: Principles and Practice, 3rd + OWL eBook 2-Semester Printed Access Card, edition: 3.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymers

    Polymers that are formed via cationic addition, anionic addition, or free-radical addition.

  • bar

    A unit of pressure equal to 105 Pa. (Section 10.2)

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • beta (b) anomer

    The cyclic hemiacetal of an aldose, in which the hydroxyl group at the anomeric position is cis to the CH2OH group.

  • beta (b) pleated sheet

    For proteins, a feature of secondary structure that forms when two or more protein chains line up side-by-side.

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • bond enthalpy

    The enthalpy change, ?H, required to break a particular bond when the substance is in the gas phase. (Section 8.8)

  • bonding molecular orbital

    A molecular orbital in which the electron density is concentrated in the internuclear region. The energy of a bonding molecular orbital is lower than the energy of the separate atomic orbitals from which it forms. (Section 9.7)

  • endothermic

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

  • enzyme

    A protein molecule that acts to catalyze specific biochemical reactions. (Section 14.7)

  • Freons

    CFCs that were heavily used for a wide variety of commercial applications, including as refrigerants, as propellants, in the production of foam insulation, as fire-fighting materials, and many other useful applications.

  • heat capacity

    The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)

  • Meso compound

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

  • n+1 rule

    In NMR spectroscopy, if n is the number of neighboring protons, then the multiplicity will be n+1.

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • stretching

    In IR spectroscopy, atype of vibration that generally produces a signal in the diagnostic region of an IR spectrum.

  • substitution reactions

    Reactions in which one group is replaced by another group.

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.