Solutions for Chapter 21.2: Structure and Bonding

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 21.2: Structure and Bonding

Solutions for Chapter 21.2
4 5 0 327 Reviews
19
0

This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 21.2: Structure and Bonding have been answered, more than 12525 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 21.2: Structure and Bonding includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Alcohol

    A compound containing an !OH (hydroxyl) group bonded to a carbon atom

  • alkyl halide

    An organic compound containing at least one halogen.

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • chemistry

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

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • crystallization.

    The process in which dissolved solute comes out of solution and forms crystals. (12.1)

  • degenerate

    Having the same energy.

  • degenerate

    A situation in which two or more orbitals have the same energy. (Section 6.7)

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • enolate

    The resonance-stabilized conjugate base of a ketone, aldehyde, or ester.

  • formation constant

    For a metal ion complex, the equilibrium constant for formation of the complex from the metal ion and base species present in solution. It is a measure of the tendency of the complex to form. (Section 17.5)

  • Frost circles

    A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.

  • Imine

    A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base

  • precipitation reaction

    A reaction that occurs between substances in solution in which one of the products is insoluble. (Section 4.2)

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • 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.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • ylide

    A compound with two oppositely charged atoms adjacent to each other.

×
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

×
Log in to StudySoup
Get Full Access to Thousands of Study Materials at Your School

Forgot password? Reset password here

Join StudySoup for FREE
Get Full Access to Thousands of Study Materials at Your School
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