Solutions for Chapter 25.5: Reactions of Amino Acids

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 25.5: Reactions of Amino Acids

Solutions for Chapter 25.5
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This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 25.5: Reactions of Amino Acids have been answered, more than 12590 students have viewed full step-by-step solutions from this chapter. Chapter 25.5: Reactions of Amino Acids includes 1 full step-by-step solutions. 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.

Key Chemistry Terms and definitions covered in this textbook
  • acyl peroxide

    A peroxide for which each oxygen atom is connected to an acyl group. Acyl peroxides are often used as radical initiators, because the O!O bond is especially weak.

  • alkanes.

    Hydrocarbons having the general formula CnH2n12, where n 5 1,2, . . . . (24.2)

  • Amino acid

    A compound that contains both an amino group and a carboxyl group

  • boiling point.

    The temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. (11.8)

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • 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.

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • Dieckmann cyclization

    An intramolecular Claisen condensation.

  • Diels-Alder adduct

    A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.

  • ionic bond

    A bond that results from the force of attraction between two oppositely charged ions.

  • isothermal process

    One that occurs at constant temperature. (Section 19.1)

  • Nonbonding electrons

    Valence electrons not involved in forming covalent bonds. Also called unshared pairs or lone pairs.

  • quantum mechanics

    A mathematical description of an electron that incorporates its wavelike properties.

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • spectroscopy

    The study of the interaction between matter and electromagnetic radiation.

  • spin-pairing energy

    The energy required to pair an electron with another electron occupying an orbital. (Section 23.6)

  • stereoisomers

    Compounds that have the same constitution but differ in the 3D arrangement of atoms.

  • Steroid

    A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.

  • structural proteins

    Fibrous proteins that are used for their structural rigidity. Examples include a-keratins found in hair, nails, skin, feathers, and wool.

  • Valence-shell electron-pair repulsion (VSEPR)

    A method for predicting bond angles based on the idea that electron pairs repel each other and keep as far apart as possible.

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