×
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 / Organic Chemistry 12

Organic Chemistry 12th Edition Solutions

Do I need to buy Organic Chemistry | 12th Edition to pass the class?

ISBN: 9781118875766

Organic Chemistry | 12th Edition - Solutions by Chapter

Do I need to buy this book?
1 Review

79% 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:

Organic Chemistry 12th Edition Student Assesment

Bernardo from Temple University 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: Organic Chemistry
Edition: 12
Author: T. W. Graham Solomons (Author), Craig B. Fryhle (Author), Scott A. Snyder (Author)
ISBN: 9781118875766

Organic Chemistry was written by and is associated to the ISBN: 9781118875766. Since problems from 0 chapters in Organic Chemistry have been answered, more than 200 students have viewed full step-by-step answer. This expansive textbook survival guide covers the following chapters: 0. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 12. The full step-by-step solution to problem in Organic Chemistry were answered by , our top Chemistry solution expert on 10/03/18, 06:29PM.

Key Chemistry Terms and definitions covered in this textbook
  • chemical kinetics

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (Chapter 14: Introduction)

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • dipole–dipole force

    A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)

  • E (Section 5.2C)

    From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides

  • electron spin

    A property of the electron that makes it behave as though it were a tiny magnet. The electron behaves as if it were spinning on its axis; electron spin is quantized. (Section 6.7)

  • 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

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • gamma radiation

    Energetic electromagnetic radiation emanating from the nucleus of a radioactive atom. (Section 21.1)

  • Ground state

    The lowest energy state of a system.

  • intermediate

    A substance formed in one elementary step of a multistep mechanism and consumed in another; it is neither a reactant nor an ultimate product of the overall reaction. (Section 14.6)

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • Phospholipid

    A lipid containing glycerol esterifi ed with two molecules of fatty acid and one molecule of phosphoric acid.

  • Reaction coordinate diagram

    A graph showing the energy changes that occur during a chemical reaction; energy is plotted on the vertical axis and reaction progress is plotted on the horizontal axis.

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

  • Strecker synthesis

    A synthetictechnique for preparing racemic a-amino acidsfrom aldehydes.

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.