Make up to $500 this semester by taking notes for StudySoup as an Elite Notetaker Apply Now

Solutions for Chapter 1.2: ClassIcal theorIes of chemIcal BondIng

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 1.2: ClassIcal theorIes of chemIcal BondIng

Since 7 problems in chapter 1.2: ClassIcal theorIes of chemIcal BondIng have been answered, more than 8061 students have viewed full step-by-step solutions from this chapter. Chapter 1.2: ClassIcal theorIes of chemIcal BondIng includes 7 full step-by-step solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781936221349. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • Aromatic compound

    A term used initially to classify benzene and its derivatives. More accurately, it is used to classify any compound that meets the Hückel criteria for aromaticity (Section 21.2A).

  • atomic mass.

    The mass of an atom in atomic mass units. (3.1)

  • Beer’s law

    In UV-Vis spectroscopy, an equation describing the relationship between molar absorptivity (e), absorbance (A), concentration (C), and path length (l): e = A (C Ž l)

  • chemical changes

    Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • Diastereotopic groups

    Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions

  • Equatorial bond

    A bond to a chair conformation of cyclohexane that extends from the ring roughly perpendicular to the imaginary axis through the center of the ring; a bond that lies roughly along the equator of a cyclohexane ring

  • gas

    Matter that has no fixed volume or shape; it conforms to the volume and shape of its container. (Section 1.2)

  • isothermal process

    One that occurs at constant temperature. (Section 19.1)

  • Lactam

    A cyclic amide.

  • nitrous acid

    A compound with molecular formula HONO.

  • oligomers

    During the polymerization process, compounds constructed from just a few monomers.

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • s-trans

    A conformation of a conjugateddiene in which the disposition of the two p bonds with regard to the connecting single bond is translike (a dihedral angle of 180°).

  • Shell

    A region of space around a nucleus that can be occupied by electrons, corresponding to a principal quantum number

  • simple lipid

    A lipid that does not undergo hydrolysis in aqueous acid or base to produce smaller fragments.

  • Vibrational infrared region

    A common type of spin-spin coupling involving the H atoms on two C atoms that are bonded to each other.

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.

×
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