×
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 9.5: Benzylic Halides, Allylic Halides, Vinylic Halides, and Aryl Halides

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 9.5: Benzylic Halides, Allylic Halides, Vinylic Halides, and Aryl Halides

This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 9.5: Benzylic Halides, Allylic Halides, Vinylic Halides, and Aryl Halides includes 4 full step-by-step solutions. Since 4 problems in chapter 9.5: Benzylic Halides, Allylic Halides, Vinylic Halides, and Aryl Halides have been answered, more than 35743 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • activity

    The decay rate of a radioactive material, generally expressed as the number of disintegrations per unit time. (Section 21.4)

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • Basicity

    An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • Confi gurational isomers

    Isomers that differ by the confi guration of substituents on an atom. Refers to the arrangement of atoms about a stereocenter

  • covalent bond

    A bond that results when two atoms share a pair of electrons.

  • 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 impact ionization (EI)

    In mass spectrometry, an ionization technique that involves bombarding a compoundwith high-energy electrons.

  • electrospray ionization (ESI):

    In mass spectrometry, an ionization technique in which the compound is first dissolved in a solvent and then sprayed via a high-voltage needle into a vacuum chamber. The tiny droplets of solution become charged by the needle, and subsequent evaporation forms gas-phase molecular ions that typically carry one or more charges.

  • Equivalent hydrogens

    Hydrogens that have the same chemical environment

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • kinetics

    A term that refers to the rate of a reaction.

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • nitrogen rule

    In mass spectrometry, an odd molecular weight indicates an odd number of nitrogen atoms in the compound, while an even molecular weight indicates either an even number of nitrogen atoms or the absence of nitrogen.

  • nitrosonium ion

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

  • potential energy

    The energy that an object possesses as a result of its composition or its position with respect to another object. (Section 5.1)

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

  • strong deactivators

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

×
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