×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 9: Organic Chemistry 8th Edition

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321768414

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Solutions for Chapter 9

Solutions for Chapter 9
4 5 0 305 Reviews
20
1
Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321768414. Chapter 9 includes 43 full step-by-step solutions. Since 43 problems in chapter 9 have been answered, more than 205918 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acid

    A substance that is able to donate a H+ ion (a proton) and, hence, increases the concentration of H+1aq2 when it dissolves in water. (Section 4.3)

  • activation energy (Ea)

    The minimum energy needed for reaction; the height of the energy barrier to formation of products. (Section 14.5)

  • amphoteric oxide.

    An oxide that exhibits both acidic and basic properties. (8.6)

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • crossed Claisen condensation

    A Claisen condensation reaction that occurs between different partners.

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • delocalization

    The spreading of a charge or lone pair as described by resonance theory.

  • Dienophile

    A compound containing a double bond (consisting of one or two C, N, or O atoms) that can react with a conjugated diene to give a Diels-Alder adduct.

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • Gibbs free energy (G)

    The ultimate arbiter of the spontaneity of a reaction, where DG = DH - T DS.

  • ionic bond

    A bond between oppositely charged ions. The ions are formed from atoms by transfer of one or more electrons. (Section 8.1)

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • peptidases

    A variety of enzymes that selectively hydrolyze specific peptide bonds.

  • reducing agent

    A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

  • thermosetting resins

    Highly crosslinked polymers that are generally very hard and insoluble.

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password