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Solutions for Chapter 24: The Organic Chemistry of the Metabolic Pathways

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 24: The Organic Chemistry of the Metabolic Pathways

Solutions for Chapter 24
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Textbook: Organic Chemistry
Edition: 8
Author: Paula Yurkanis Bruice
ISBN: 9780134042282

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Since 54 problems in chapter 24: The Organic Chemistry of the Metabolic Pathways have been answered, more than 33202 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 24: The Organic Chemistry of the Metabolic Pathways includes 54 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780134042282.

Key Chemistry Terms and definitions covered in this textbook
  • a-Helix

    A type of secondary structure in which a section of polypeptide chain coils into a spiral, most commonly a right-handed spiral.

  • Activating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.

  • alkenes.

    Hydrocarbons that contain one or more carbon-carbon double bonds. They have the general formula CnH2n, where n 5 2,3, . . . . (24.2)

  • aqueous solution.

    A solution in which the solvent is water. (4.1)

  • aryl amine

    An amine in which the nitrogen atom is connected directly to an aromatic ring.

  • Avogadro’s number (NA)

    The number of 12C atoms in exactly 12 g of 12C; it equals 6.022 * 1023 mol-1. (Section 3.4)

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • 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

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • isotopes

    Atoms of the same element containing different numbers of neutrons and therefore having different masses. (Section 2.3)

  • Ketone

    A compound containing a carbonyl group bonded to two carbons.

  • node

    Points in an atom at which the electron density is zero. For example, the node in a 2s orbital is a spherical surface. (Section 6.6)

  • Oligosaccharide

    A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.

  • paramagnetism

    A property that a substance possesses if it contains one or more unpaired electrons. A paramagnetic substance is drawn into a magnetic field. (Section 9.8)

  • physical changes

    Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)

  • syn-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 0°.

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

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