×
Log in to StudySoup
Get Full Access to
Join StudySoup for FREE
Get Full Access to

Already have an account? Login here
×
Reset your password

Textbooks / Chemistry / Chemistry Principles and Practice 54256

Chemistry Principles and Practice 54256th Edition Solutions

Do I need to buy Chemistry Principles and Practice | 54256th Edition to pass the class?

ISBN: 9780534420123

Chemistry Principles and Practice | 54256th Edition - Solutions by Chapter

Do I need to buy this book?
1 Review

72% of students who have bought this book said that they did not need the hard copy to pass the class. Were they right? Add what you think:

Chemistry Principles and Practice 54256th Edition Student Assesment

Daren from University of Texas at Arlington said

"If I knew then what I knew now I would not have bought the book. It was over priced and My professor only used it a few times."

Textbook: Chemistry Principles and Practice
Edition: 54256
Author: Daniel L.; Goode, Scott R.; Ball, David W. Reger (Author)
ISBN: 9780534420123

The full step-by-step solution to problem in Chemistry Principles and Practice 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: Chemistry Principles and Practice, edition: 54256. Chemistry Principles and Practice was written by and is associated to the ISBN: 9780534420123. Since problems from 0 chapters in Chemistry Principles and Practice have been answered, more than 200 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • atomic number (Z).

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

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • Carboxyl group (Section 1.3D)

    A !COOH group.

  • Coulomb’s law.

    The potential energy between two ions is directly proportional to the product of their charges and inversely proportional to the distance between them. (9.3)

  • curved arrows

    Tools that are used for drawing resonance structures and for showing the flow of electron density during each step of a reaction mechanism.

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • Fluid-mosaic model

    A biological membrane that consists of a phospholipid bilayer with proteins, carbohydrates, and other lipids on the surface and embedded in the bilayer

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • interstitial alloy

    An alloy in which smaller atoms fit into spaces between larger atoms. The larger atoms are metallic elements and the smaller atoms are typically nonmetallic elements. (Section 12.3)

  • Lactam

    A cyclic amide.

  • nematic liquid crystalline phase

    A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)

  • oxonium ion

    An intermediate with a positively charged oxygen atom.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

  • vinylic

    The carbon atoms of a carbon-carbon double bond.

  • weak deactivators

    Groups that weakly deactivate an aromatic ring toward electrophilic aromatic substitution, thereby decreasing the rate of the reaction.