Solutions for Chapter 17: Carboxylic Acids

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 17: Carboxylic Acids

Solutions for Chapter 17
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 48 problems in chapter 17: Carboxylic Acids have been answered, more than 4602 students have viewed full step-by-step solutions from this chapter. Chapter 17: Carboxylic Acids includes 48 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • atomic radius.

    One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • dash

    In bond-line structures, agroup going behind the page.

  • electron configuration

    The arrangement of electrons in the orbitals of an atom or molecule (Section 6.8)

  • Fourier transform NMR (FT-NMR)

    The modern NMR method that is based on a constant magnetic fi eld, a short pulse of electromagnetic radiation, and a mathematical Fourier transform to produce the spectrum

  • hydrophilic

    A polar group that has favorable interactions with water.

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • molecular compound

    A compound that consists of molecules. (Section 2.6)

  • nonpolar covalent bond

    A covalent bond in which the electrons are shared equally. (Section 8.4) normal boiling point The boiling point at 1 atm pressure. (Section 11.5)

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • para

    On an aromatic ring, the C4position.

  • Phasing

    The sign of the wave function at particular coordinates in space, either plus or minus. Phasing is often represented by colors, such as red or blue

  • pi (p) bond

    A bond formed from adjacent, overlapping p orbitals.

  • Pi (p) molecular orbital

    A molecular orbital formed by overlapping parallel 2p orbitals on adjacent atoms; its electron density lies above and below the line connecting the atoms

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • sp3-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with three p orbitals to form four hybridized atomic orbitals.

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

  • Zaitsev’s rule

    A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond

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