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Organic Chemistry 7th Edition - Solutions by Chapter

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Organic Chemistry | 7th Edition - Solutions by Chapter

The full step-by-step solution to problem in Organic Chemistry were answered by Patricia, our top Chemistry solution expert on 03/16/18, 05:02PM. This expansive textbook survival guide covers the following chapters: 24. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since problems from 24 chapters in Organic Chemistry have been answered, more than 5508 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • Addition reaction

    A reaction in which two atoms or groups of atoms react with a double bond, forming a compound with the two new groups bonded to the carbons of the original double bond.

  • atmosphere (atm)

    A unit of pressure equal to 760 torr; 1 atm = 101.325 kPa. (Section 10.2) atom The smallest representative particle of an element. (Sections 1.1 and 2.1)

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • chair conformation

    The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered.

  • chlor-alkali process.

    The production of chlorine gas by the electrolysis of aqueous NaCl solution. (22.6)

  • conjugate base

    A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

  • Coupling constant

    The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • 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

  • Fourier transform NMR (FT-NMR)

    The modern NMR method that is based on a constant magnetic fi eld, a short pulse of electromagnetic radiation, and a mathematical Fourier transform to produce the spectrum

  • ideal solution

    A solution that obeys Raoult’s law. (Section 13.5)

  • low-spin complex

    A metal complex in which the electrons are paired in lower-energy orbitals. (Section 23.6)

  • molecular-orbital diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived; also called an energy-level diagram. (Section 9.7)

  • polar molecule

    A molecule that possesses a nonzero dipole moment. (Section 8.4)

  • quaternary ammonium salt

    An ionic compound containing a positively charged nitrogen atom connected to four alkyl groups.

  • secondary

    A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • unsaturated

    A compound containingone or more p bonds.

  • weak activators

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

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