Solutions for Chapter 14.7: Retrosynthetic Analysis and Grignard and Organolithium Reagents

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 14.7: Retrosynthetic Analysis and Grignard and Organolithium Reagents

Solutions for Chapter 14.7
4 5 0 369 Reviews
16
4

Chapter 14.7: Retrosynthetic Analysis and Grignard and Organolithium Reagents includes 1 full step-by-step solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 14.7: Retrosynthetic Analysis and Grignard and Organolithium Reagents have been answered, more than 10850 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • Aramid

    A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • battery.

    A galvanic cell, or a series of combined galvanic cells, that can be used as a source of direct electric current at a constant voltage. (18.6)

  • becquerel

    The SI unit of radioactivity. It corresponds to one nuclear disintegration per second. (Section 21.4)

  • common ion effect.

    The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substances. (16.2)

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • constructive interference

    When two waves interact with each other in a way that produces a wave with a larger amplitude.

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • Energy diagram

    A graph showing the changes in energy that occur during a chemical reaction; energy is plotted on the vertical axis, and reaction progress is plotted on the horizontal axis. Also called a reaction coordinate diagram

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • inversion of configuration

    During a reaction, when the configuration of a chirality center is changed.

  • ion

    Electrically charged atom or group of atoms (polyatomic ion); ions can be positively or negatively charged, depending on whether electrons are lost (positive) or gained (negative) by the atoms. (Section 2.7)

  • mineral

    A solid, inorganic substance occurring in nature, such as calcium carbonate, which occurs as calcite. (Section 23.1)

  • noble gases

    Members of group 8A in the periodic table. (Section 7.8)

  • rate law

    An equation that relates the reaction rate to the concentrations of reactants (and sometimes of products also). (Section 14.3)

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • tetrahedral intermediate

    An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.

  • thermoplastics

    Polymers that are hard at room temperature but soft when heated.

×
Log in to StudySoup
Get Full Access to Organic Chemistry,

Forgot password? Reset password here

Join StudySoup for FREE
Get Full Access to Organic Chemistry,
Join with Email
Already have an account? Login here
Reset your password

I don't want to reset my password

Need help? Contact support

Need an Account? Is not associated with an account
Sign up
We're here to help

Having trouble accessing your account? Let us help you, contact support at +1(510) 944-1054 or support@studysoup.com

Got it, thanks!
Password Reset Request Sent An email has been sent to the email address associated to your account. Follow the link in the email to reset your password. If you're having trouble finding our email please check your spam folder
Got it, thanks!
Already have an Account? Is already in use
Log in
Incorrect Password The password used to log in with this account is incorrect
Try Again

Forgot password? Reset it here