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Solutions for Chapter 25.7: Peptides

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 25.7: Peptides

Since 5 problems in chapter 25.7: Peptides have been answered, more than 36304 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 25.7: Peptides includes 5 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-adduct

    The product obtainedfrom 1,2-addition across a conjugated p system.

  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • coupling constant

    When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.

  • degenerate orbitals

    Orbitals that have the same energy.

  • delocalized molecular orbitals.

    Molecular orbitals that are not confined between two adjacent bonding atoms but actually extend over three or more atoms. (10.8)

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • enol

    A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • ion

    Electrically charged atom or group of atoms (polyatomic ion); ions can be positively or negatively charged, depending on whether electrons are lost (positive) or gained (negative) by the atoms. (Section 2.7)

  • Mercaptan

    A common name for a thiol; that is, any compound that contains an -SH (sulfhydryl) group

  • methylene group

    A CH2 group.

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • phenyl group

    A C6H5 group.

  • primary structure

    For proteins, the sequence of amino acid residues.

  • radioisotope

    An isotope that is radioactive; that is, it is undergoing nuclear changes with emission of radiation. (Section 21.1)

  • scientific method

    The general process of advancing scientific knowledge by making experimental observations and by formulating hypotheses, theories, and laws. (Section 1.3)

  • tosylate

    An excellent leaving group (OTs). transition state (Sect. 6.6): A state through which a reaction passes. On an energy diagram, a transition state corresponds with a local maximum.

  • Williamson ether synthesis

    A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).

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