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Solutions for Chapter 11.16: Benzylic Side Chains and Retrosynthetic Analysis

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 11.16: Benzylic Side Chains and Retrosynthetic Analysis

Solutions for Chapter 11.16
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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. Since 1 problems in chapter 11.16: Benzylic Side Chains and Retrosynthetic Analysis have been answered, more than 29229 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 11.16: Benzylic Side Chains and Retrosynthetic Analysis includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Amorphous domain

    A disordered, noncrystalline region in the solid state of a polymer.

  • autooxidation

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

  • bent

    A type of geometry resulting from an sp3-hybridized atom that has two lone pairs. For example, the oxygen atom in H2O.

  • bond order.

    The difference between the numbers of electrons in bonding molecular orbitals and antibonding molecular orbitals, divided by two. (10.7)

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • 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)

  • degenerate

    Having the same energy.

  • diagonal relationship.

    Similarities between pairs of elements in different groups and periods of the periodic table. (8.6)

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • Ether

    A compound containing an oxygen atom bonded to two carbon atoms.

  • Friedel-Crafts reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • Levorotatory

    Refers to a substance that rotates the plane of polarized light to the left.

  • Monomer

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

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • tertiary alkyl halide

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

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • thiols

    Compounds containing a mercapto group (SH).

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