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Solutions for Chapter 14: The proton NMR spectrum of a compound with the formula C7H12O2 is shown. The infrared spectrum displays a strong band at 1738 cm21 and a weak band at 1689 cm21. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of th

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9781305080485

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Solutions for Chapter 14: The proton NMR spectrum of a compound with the formula C7H12O2 is shown. The infrared spectrum displays a strong band at 1738 cm21 and a weak band at 1689 cm21. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of th

Solutions for Chapter 14
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Textbook: Organic Chemistry
Edition: 9
Author: John E. McMurry
ISBN: 9781305080485

This expansive textbook survival guide covers the following chapters and their solutions. Since 161 problems in chapter 14: The proton NMR spectrum of a compound with the formula C7H12O2 is shown. The infrared spectrum displays a strong band at 1738 cm21 and a weak band at 1689 cm21. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of th have been answered, more than 59528 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781305080485. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Chapter 14: The proton NMR spectrum of a compound with the formula C7H12O2 is shown. The infrared spectrum displays a strong band at 1738 cm21 and a weak band at 1689 cm21. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of th includes 161 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Acyl group

    An RCO! or ArCO! group.

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • carbides.

    Ionic compounds containing the C2 22 or C42 ion. (22.3)

  • cation.

    An ion with a net positive charge. (2.5)

  • concentration

    The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)

  • crystallization.

    The process in which dissolved solute comes out of solution and forms crystals. (12.1)

  • energy-level diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)

  • fibrous proteins

    Proteins that consist of linear chains that are bundled together.

  • immiscible liquids

    Liquids that do not dissolve in one another to a significant extent. (Section 13.3)

  • Ionization potential (IP)

    The minimum energy required to remove an electron from an atom or molecule to a distance where there is no electrostatic interaction between the resulting ion and electron.

  • leaving group

    A group capable ofseparating from a compound.

  • locant

    In nomenclature, a numberused to identify the location of a substituent.

  • magnetic moment

    A magneticfield generated by a spinning proton.

  • metallic character

    The extent to which an element exhibits the physical and chemical properties characteristic of metals, for example, luster, malleability, ductility, and good thermal and electrical conductivity. (Section 7.6)

  • porphyrin

    A complex derived from the porphine molecule. (Section 23.3)

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • radical

    A chemical entity with an unpaired electron.

  • Thermolysis

    Cleavage by heating

  • Valence shell

    The outermost occupied electron shell of an atom.

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.

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