×
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 10.4: Allylic Anions

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 10.4: Allylic Anions

Solutions for Chapter 10.4
4 5 0 269 Reviews
16
2

Since 1 problems in chapter 10.4: Allylic Anions have been answered, more than 36443 students have viewed full step-by-step solutions from this chapter. Chapter 10.4: Allylic Anions includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • acetal

    A functional group characterized by two alkoxy (OR) groups connected to the same carbon atom.Acetals can be used as protecting groups for aldehydes or ketones.

  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • Anti stereoselectivity

    The addition of atoms or groups of atoms to opposite faces of a carbon-carbon double bond.

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • Brønsted-Lowry base

    A proton acceptor

  • cell potential

    The potential difference between the cathode and anode in an electrochemical cell; it is measured in volts: 1 V = 1 J>C. Also called electromotive force. (Section 20.4)

  • Chair conformation

    The most stable nonplanar conformation of a cyclohexane ring; all bond angles are approximately 109.5°, and all bonds on adjacent carbons are staggered.

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • geminal

    Two groups connected to the same carbon atom. For example, a geminal dihalide is a compound with two halogens connected to the same carbon atom.

  • Grignard reagent

    A carbanion with the structure RMgX.

  • Hofmann elimination

    A reaction in which an amino group is treated with excess methyl iodide, thereby converting it into an excellent leaving group, followed by treatment with a strong base to give an E2 reaction that yields an alkene.

  • hydrazone

    A compound with the structure R2CRN!NH2.

  • Lactone

    A cyclic ester.

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • Regioselective reaction

    An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • saturated

    A compound that contains no p bonds.

  • Twist-boat conformation

    A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.

×
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